Temat: "HEK293 Cells" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: A microfabricated lab-on-chip with three-dimensional electrodes for microscopic observation of bioelectromagnetic effects of cells.
Autorzy:: Lu Y; Beijing Advanced Innovation Center for Structural Biology & Frontier Research Center for Biological Structure, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China. Electronic address: .
Shi Y; Beijing Advanced Innovation Center for Structural Biology & Frontier Research Center for Biological Structure, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China; Westlake Laboratory of Life Sciences and Biomedicine, Xihu District, Hangzhou 310024, Zhejiang Province, China; Key Laboratory of Structural Biology of Zhejiang Province, School of Life Sciences, Westlake University, Institute of Biology, Westlake Institute for Advanced Study, 18 Shilongshan Road, Hangzhou 310024, Zhejiang Province, China. Electronic address: .; Pokaż więcej
Źródło:: Bioelectrochemistry (Amsterdam, Netherlands) [Bioelectrochemistry] 2023 Dec; Vol. 154, pp. 108554. Date of Electronic Publication: 2023 Aug 28.
Typ publikacji:: Journal Article
MeSH Terms:: HEK293 Cells*
Humans ; Cell Proliferation ; Cell Cycle ; Computer Simulation ; Electrodes

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Tytuł:: Enhanced ER protein processing gene expression increases rAAV yield and full capsid ratio in HEK293 cells.
Autorzy:: Fu Q; Department of Biomedical Engineering and Biotechnology, University of Massachusetts Lowell, Lowell, MA, 01854, USA.
Wang Y; Department of Chemical Engineering, University of Massachusetts Lowell, Lowell, MA, 01854, USA.
Qin J; Department of Biomedical Engineering and Biotechnology, University of Massachusetts Lowell, Lowell, MA, 01854, USA.
Xie D; Department of Chemical Engineering, University of Massachusetts Lowell, Lowell, MA, 01854, USA.
McNally D; Department of Chemical Engineering, University of Massachusetts Lowell, Lowell, MA, 01854, USA.; MassBiologics, University of Massachusetts Chan Medical School, Mattapan, MA, 02126, USA.
Yoon S; Department of Biomedical Engineering and Biotechnology, University of Massachusetts Lowell, Lowell, MA, 01854, USA. seongkyu_.; Department of Chemical Engineering, University of Massachusetts Lowell, Lowell, MA, 01854, USA. seongkyu_.; Pokaż więcej
Źródło:: Applied microbiology and biotechnology [Appl Microbiol Biotechnol] 2024 Sep 04; Vol. 108 (1), pp. 459. Date of Electronic Publication: 2024 Sep 04.
Typ publikacji:: Journal Article
MeSH Terms:: Dependovirus*/genetics
X-Box Binding Protein 1*/genetics
X-Box Binding Protein 1*/metabolism
Endoplasmic Reticulum*/metabolism
Genetic Vectors*/genetics
Humans ; HEK293 Cells ; Gene Expression ; Protein Phosphatase 1/genetics ; Protein Phosphatase 1/metabolism ; Proto-Oncogene Proteins c-bcl-2/genetics ; Proto-Oncogene Proteins c-bcl-2/metabolism ; Capsid/metabolism

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Tytuł:: Phosphorylation of phospholamban promotes SERCA2a activation by dwarf open reading frame (DWORF).
Autorzy:: Bovo E; Department of Cell and Molecular Physiology, Loyola University Chicago, Stritch School of Medicine, 2160 South First Avenue, Maywood, IL 60153, USA. Electronic address: .
Jamrozik T; Department of Cell and Molecular Physiology, Loyola University Chicago, Stritch School of Medicine, 2160 South First Avenue, Maywood, IL 60153, USA.
Kahn D; Department of Cell and Molecular Physiology, Loyola University Chicago, Stritch School of Medicine, 2160 South First Avenue, Maywood, IL 60153, USA.
Karkut P; Department of Cell and Molecular Physiology, Loyola University Chicago, Stritch School of Medicine, 2160 South First Avenue, Maywood, IL 60153, USA.
Robia SL; Department of Cell and Molecular Physiology, Loyola University Chicago, Stritch School of Medicine, 2160 South First Avenue, Maywood, IL 60153, USA.
Zima AV; Department of Cell and Molecular Physiology, Loyola University Chicago, Stritch School of Medicine, 2160 South First Avenue, Maywood, IL 60153, USA.; Pokaż więcej
Źródło:: Cell calcium [Cell Calcium] 2024 Jul; Vol. 121, pp. 102910. Date of Electronic Publication: 2024 May 24.
Typ publikacji:: Journal Article
MeSH Terms:: Sarcoplasmic Reticulum Calcium-Transporting ATPases*/metabolism
Calcium-Binding Proteins*/metabolism
Humans ; Phosphorylation ; HEK293 Cells ; Open Reading Frames/genetics ; Calcium/metabolism ; Enzyme Activation ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism ; Cyclic AMP-Dependent Protein Kinases/metabolism

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Tytuł:: Enhanced sensitivity of chimeric insect olfactory co-receptors for detecting odorant molecules.
Autorzy:: Takaku T; Environmental Health Science Laboratory, Sumitomo Chemical Co., Ltd., 1-98, 3-Chome, Kasugade-Naka, Konohana-Ku, Osaka, 554-8558, Japan. Electronic address: .
Tonooka Y; Environmental Health Science Laboratory, Sumitomo Chemical Co., Ltd., 1-98, 3-Chome, Kasugade-Naka, Konohana-Ku, Osaka, 554-8558, Japan.
Takahashi Y; Environmental Health Science Laboratory, Sumitomo Chemical Co., Ltd., 1-98, 3-Chome, Kasugade-Naka, Konohana-Ku, Osaka, 554-8558, Japan.
Kitamoto S; Environmental Health Science Laboratory, Sumitomo Chemical Co., Ltd., 1-98, 3-Chome, Kasugade-Naka, Konohana-Ku, Osaka, 554-8558, Japan.; Pokaż więcej
Źródło:: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2024 Sep 24; Vol. 726, pp. 150273. Date of Electronic Publication: 2024 Jun 15.
Typ publikacji:: Journal Article
MeSH Terms:: Receptors, Odorant*/genetics
Receptors, Odorant*/metabolism
Receptors, Odorant*/chemistry
Odorants*/analysis
Animals ; Drosophila melanogaster/genetics ; Drosophila melanogaster/metabolism ; Bombyx/genetics ; Bombyx/metabolism ; Aedes/genetics ; Aedes/metabolism ; Recombinant Fusion Proteins/metabolism ; Recombinant Fusion Proteins/genetics ; Recombinant Fusion Proteins/chemistry ; Insect Proteins/genetics ; Insect Proteins/metabolism ; Insect Proteins/chemistry ; Bees/metabolism ; Bees/genetics ; HEK293 Cells ; Octanols

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Tytuł:: Identification of a novel target of sulforaphane: Sulforaphane binds to acyl-protein thioesterase 2 (APT2) and attenuates its palmitoylation.
Autorzy:: Kodaka M; Department of Agricultural Chemistry, Faculty of Applied Biosciences, Tokyo University of Agriculture, Tokyo, Japan. Electronic address: .
Kikuchi A; Department of Agricultural Chemistry, Faculty of Applied Biosciences, Tokyo University of Agriculture, Tokyo, Japan. Electronic address: .
Kawahira K; Department of Agricultural Chemistry, Faculty of Applied Biosciences, Tokyo University of Agriculture, Tokyo, Japan. Electronic address: .
Kamada H; Laboratory of Biopharmaceutical Research, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka, Japan. Electronic address: .
Katsuta R; Department of Chemistry for Life Sciences and Agriculture, Tokyo University of Agriculture, Tokyo, Japan. Electronic address: .
Ishigami K; Department of Chemistry for Life Sciences and Agriculture, Tokyo University of Agriculture, Tokyo, Japan. Electronic address: .
Suzuki T; Department of Agricultural Chemistry, Faculty of Applied Biosciences, Tokyo University of Agriculture, Tokyo, Japan. Electronic address: .
Yamamoto Y; Department of Agricultural Chemistry, Faculty of Applied Biosciences, Tokyo University of Agriculture, Tokyo, Japan. Electronic address: .
Inoue J; Department of Agricultural Chemistry, Faculty of Applied Biosciences, Tokyo University of Agriculture, Tokyo, Japan. Electronic address: .; Pokaż więcej
Źródło:: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2024 Sep 24; Vol. 726, pp. 150244. Date of Electronic Publication: 2024 Jun 19.
Typ publikacji:: Journal Article
MeSH Terms:: Isothiocyanates*/metabolism
Isothiocyanates*/pharmacology
Isothiocyanates*/chemistry
Sulfoxides*/pharmacology
Sulfoxides*/metabolism
Sulfoxides*/chemistry
Thiolester Hydrolases*/metabolism
Thiolester Hydrolases*/chemistry
Lipoylation*/drug effects
Humans ; Protein Binding ; HEK293 Cells ; Cell Membrane/metabolism

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Tytuł:: Orthogonal characterization of rAAV9 reveals unexpected transgene heterogeneity.
Autorzy:: Eisenhut P; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Andorfer P; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Haid A; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Jokl B; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Manhartsberger R; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Fuchsberger F; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Innthaler B; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Lengler J; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Kraus B; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Pletzenauer R; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria.
Hernandez Bort JA; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria; Department of Analytical Chemistry, University of Vienna, Vienna 1090, Austria. Electronic address: .
Unterthurner S; Gene Therapy Process Development, Baxalta Innovations GmbH, part of Takeda companies, Orth an der Donau, Orth an der Donau 2304, Austria. Electronic address: .; Pokaż więcej
Źródło:: Journal of biotechnology [J Biotechnol] 2024 Sep 20; Vol. 393, pp. 128-139. Date of Electronic Publication: 2024 Aug 04.
Typ publikacji:: Journal Article
MeSH Terms:: Dependovirus*/genetics
Transgenes*
Genetic Vectors*/genetics
Humans ; HEK293 Cells ; Transfection/methods ; Genome, Viral/genetics ; Genetic Therapy/methods

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Skocz do pozycji: 7.

Tytuł:: Structural insights into the allosteric effects of the antiepileptic drug topiramate on the Ca V 2.3 channel.
Autorzy:: Gao Y; Key Laboratory of Biomacromolecules (CAS), National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.
Bai Q; Key Laboratory of Biomacromolecules (CAS), National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.
Zhang XC; Key Laboratory of Biomacromolecules (CAS), National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China. Electronic address: .
Zhao Y; Key Laboratory of Biomacromolecules (CAS), National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China; State Key Laboratory of Brain and Cognitive Science, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China. Electronic address: .; Pokaż więcej
Źródło:: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2024 Sep 17; Vol. 725, pp. 150271. Date of Electronic Publication: 2024 Jun 15.
Typ publikacji:: Journal Article
MeSH Terms:: Anticonvulsants*/chemistry
Anticonvulsants*/pharmacology
Topiramate*/chemistry
Topiramate*/pharmacology
Cryoelectron Microscopy*
Calcium Channels, R-Type*/chemistry
Calcium Channels, R-Type*/metabolism
Humans ; Allosteric Regulation/drug effects ; Binding Sites ; Models, Molecular ; HEK293 Cells ; Protein Conformation ; Fructose/chemistry ; Fructose/analogs & derivatives ; Fructose/metabolism ; Animals ; Cation Transport Proteins

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Skocz do pozycji: 8.

Tytuł:: RNF8-mediated multi-ubiquitination of MCM7: Linking disassembly of the CMG helicase with DNA damage response in human cells.
Autorzy:: Sun Q; State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, Beijing 10005, China.
Sui Y; School of Life Sciences, Chongqing University; Chongqing 401331, China.
Li S; School of Life Sciences, Chongqing University; Chongqing 401331, China.
Zhou R; School of Life Sciences, Chongqing University; Chongqing 401331, China.
Fu Z; School of Life Sciences, Chongqing University; Chongqing 401331, China.
Luo J; School of Life Sciences, Chongqing University; Chongqing 401331, China.
Zhao W; School of Life Sciences, Chongqing University; Chongqing 401331, China. Electronic address: .; Pokaż więcej
Źródło:: Life sciences [Life Sci] 2024 Sep 15; Vol. 353, pp. 122912. Date of Electronic Publication: 2024 Jul 14.
Typ publikacji:: Journal Article
MeSH Terms:: Ubiquitin-Protein Ligases*/metabolism
Ubiquitin-Protein Ligases*/genetics
Ubiquitination*
DNA Damage*
Minichromosome Maintenance Complex Component 7*/metabolism
Minichromosome Maintenance Complex Component 7*/genetics
DNA-Binding Proteins*/metabolism
DNA-Binding Proteins*/genetics
DNA Replication*
Humans ; BRCA1 Protein/metabolism ; BRCA1 Protein/genetics ; HEK293 Cells ; DNA Repair ; HeLa Cells

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Skocz do pozycji: 9.

Tytuł:: Detachable acoustofluidic droplet-sorter.
Autorzy:: Das D; Department of Biomedical Engineering, National Cheng Kung University, Tainan, 701, Taiwan.
Huang SH; Department of Biochemistry and Molecular Biology, College of Medicine, National Cheng Kung University, Tainan, 701, Taiwan; Institute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan, 701, Taiwan.
Weng CL; Department of Mechanical Engineering, National Cheng Kung University, Tainan, 701, Taiwan.
Yu CH; Department of Biochemistry and Molecular Biology, College of Medicine, National Cheng Kung University, Tainan, 701, Taiwan; Institute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan, 701, Taiwan.
Hsu CK; Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, 701, Taiwan.
Lee YC; Department of Mechanical Engineering, National Cheng Kung University, Tainan, 701, Taiwan.
Cheng HC; Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, 701, Taiwan.
Chuang HS; Department of Biomedical Engineering, National Cheng Kung University, Tainan, 701, Taiwan; Medical Device Innovation Center, National Cheng Kung University, Tainan, 701, Taiwan. Electronic address: .; Pokaż więcej
Źródło:: Analytica chimica acta [Anal Chim Acta] 2024 Sep 08; Vol. 1321, pp. 343043. Date of Electronic Publication: 2024 Jul 31.
Typ publikacji:: Journal Article
MeSH Terms:: Acoustics*/instrumentation
Cell Survival*
Humans ; HEK293 Cells ; Microfluidic Analytical Techniques/instrumentation ; Flow Cytometry/instrumentation ; Lab-On-A-Chip Devices ; Single-Cell Analysis/instrumentation ; Cell Separation/instrumentation ; Cell Separation/methods ; Equipment Design

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Tytuł:: Discovery of pyridazinone derivatives bearing tetrahydroimidazo[1,2-a]pyrazine scaffold as potent inhibitors of transient receptor potential canonical 5 to ameliorate hypertension-induced renal injury in rats.
Autorzy:: Xu Y; School of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, 210046, China; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Ren Y; State Key Laboratory of Natural Medicines and Jiangsu Provincial Key Laboratory for TCM Evaluation and Translational Development, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, 211198, China.
Zhang J; State Key Laboratory of Natural Medicines and Jiangsu Provincial Key Laboratory for TCM Evaluation and Translational Development, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, 211198, China.
Niu B; State Key Laboratory of Natural Medicines and Jiangsu Provincial Key Laboratory for TCM Evaluation and Translational Development, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, 211198, China.
Liu M; State Key Laboratory of Natural Medicines and Jiangsu Provincial Key Laboratory for TCM Evaluation and Translational Development, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, 211198, China.
Xu T; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Zhang X; State Key Laboratory of Natural Medicines and Jiangsu Provincial Key Laboratory for TCM Evaluation and Translational Development, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, 211198, China.
Shen J; School of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, 210046, China; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Wang K; State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. Electronic address: .
Cao Z; State Key Laboratory of Natural Medicines and Jiangsu Provincial Key Laboratory for TCM Evaluation and Translational Development, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, 211198, China. Electronic address: .; Pokaż więcej
Źródło:: European journal of medicinal chemistry [Eur J Med Chem] 2024 Sep 05; Vol. 275, pp. 116565. Date of Electronic Publication: 2024 Jun 04.
Typ publikacji:: Journal Article
MeSH Terms:: Pyrazines*/chemistry
Pyrazines*/pharmacology
Pyrazines*/chemical synthesis
TRPC Cation Channels*/antagonists & inhibitors
TRPC Cation Channels*/metabolism
Hypertension*/drug therapy
Animals ; Humans ; Rats ; HEK293 Cells ; Structure-Activity Relationship ; Male ; Drug Discovery ; Molecular Structure ; Pyridazines/pharmacology ; Pyridazines/chemistry ; Pyridazines/chemical synthesis ; Dose-Response Relationship, Drug ; Antihypertensive Agents/pharmacology ; Antihypertensive Agents/chemistry ; Antihypertensive Agents/chemical synthesis ; Rats, Sprague-Dawley ; Imidazoles/chemistry ; Imidazoles/pharmacology ; Imidazoles/chemical synthesis

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Tytuł:: Agonist Discovery for Membrane Proteins on Live Cells by Using DNA-encoded Libraries.
Autorzy:: Huang Y; Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR 999077, China.
Hou R; Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR 999077, China.; Laboratory for Synthetic Chemistry and Chemical Biology Limited, , Innovation and Technology Commission, Units 1503-1511, 15/F., Building 17W, Hong Kong SAR 999077, China.
Lam FS; Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR 999077, China.
Jia Y; Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR 999077, China.
Zhou Y; Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR 999077, China.; Laboratory for Synthetic Chemistry and Chemical Biology Limited, , Innovation and Technology Commission, Units 1503-1511, 15/F., Building 17W, Hong Kong SAR 999077, China.
He X; Shenzhen NewDEL Biotech Co., Ltd., Shenzhen 518110, China.
Li G; Institute of Systems and Physical Biology, Shenzhen Bay Laboratory, Shenzhen 518000, China.
Xiong F; Shenzhen NewDEL Biotech Co., Ltd., Shenzhen 518110, China.
Cao Y; School of Pharmacy, Naval Medical University, Shanghai 200433, China.
Wang D; School of Pharmacy, Naval Medical University, Shanghai 200433, China.
Li X; Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR 999077, China.; Laboratory for Synthetic Chemistry and Chemical Biology Limited, , Innovation and Technology Commission, Units 1503-1511, 15/F., Building 17W, Hong Kong SAR 999077, China.; Pokaż więcej
Źródło:: Journal of the American Chemical Society [J Am Chem Soc] 2024 Sep 04; Vol. 146 (35), pp. 24638-24653. Date of Electronic Publication: 2024 Aug 22.
Typ publikacji:: Journal Article
MeSH Terms:: Receptor, Insulin*/agonists
Receptor, Insulin*/metabolism
Small Molecule Libraries*/pharmacology
Small Molecule Libraries*/chemistry
Small Molecule Libraries*/chemical synthesis
DNA*/chemistry
DNA*/metabolism
ErbB Receptors*/metabolism
ErbB Receptors*/agonists
Humans ; Membrane Proteins/agonists ; Membrane Proteins/metabolism ; Drug Discovery ; HEK293 Cells ; Ligands ; Antigens, CD

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Skocz do pozycji: 12.

Tytuł:: Finely ordered intracellular domain harbors an allosteric site to modulate physiopathological function of P2X3 receptors.
Autorzy:: Lin YY; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Lu Y; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Li CY; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Ma XF; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Shao MQ; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Gao YH; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Zhang YQ; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Jiang HN; Departments of Chemical Biology and Pharmacology, College of Basic Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Liu Y; Departments of Chemical Biology and Pharmacology, College of Basic Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yang Y; Departments of Chemical Biology and Pharmacology, College of Basic Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Huang LD; Departments of Chemical Biology and Pharmacology, College of Basic Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Cao P; Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Wang HS; State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, Collaborative Innovation Center for Guangxi Ethnic Medicine, School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University, Guilin, China. .
Wang J; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China. .; School of Science, China Pharmaceutical University, Nanjing, China. .
Yu Y; School of Basic Medicine and Clinical Pharmacy, and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China. .; Departments of Chemical Biology and Pharmacology, College of Basic Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai, China. .; Key Laboratory of Preclinical Study for New Drugs of Gansu Province, School of Basic Medical Sciences, Lanzhou University, Lanzhou, China. .; Pokaż więcej
Źródło:: Nature communications [Nat Commun] 2024 Sep 03; Vol. 15 (1), pp. 7652. Date of Electronic Publication: 2024 Sep 03.
Typ publikacji:: Journal Article
MeSH Terms:: Receptors, Purinergic P2X3*/metabolism
Receptors, Purinergic P2X3*/chemistry
Receptors, Purinergic P2X3*/genetics
Allosteric Site*
Protein Domains*
Animals ; Humans ; Mice ; HEK293 Cells ; Adenosine Triphosphate/metabolism ; Male ; Mice, Inbred C57BL ; Allosteric Regulation

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Tytuł:: Molecular mechanism of IKK catalytic dimer docking to NF-κB substrates.
Autorzy:: Li C; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France.
Moro S; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France.
Shostak K; Laboratory of Cancer Biology, GIGA Cancer, University of Liege, CHU, Sart-Tilman, 4000, Liege, Belgium.
O'Reilly FJ; Institute of Biotechnology, Technische Universität Berlin, Gustav-Meyer-Allee 25, Berlin, Germany.
Donzeau M; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France.
Graziadei A; Institute of Biotechnology, Technische Universität Berlin, Gustav-Meyer-Allee 25, Berlin, Germany.
McEwen AG; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) / INSERM UMR-S 1258 / CNRS UMR7104/ Université de Strasbourg, 1 rue Laurent Fries, 67400, Illkirch, France.
Desplancq D; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France.
Poussin-Courmontagne P; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) / INSERM UMR-S 1258 / CNRS UMR7104/ Université de Strasbourg, 1 rue Laurent Fries, 67400, Illkirch, France.
Bachelart T; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France.
Fiskin M; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France.
Berrodier N; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) / INSERM UMR-S 1258 / CNRS UMR7104/ Université de Strasbourg, 1 rue Laurent Fries, 67400, Illkirch, France.
Pichard S; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) / INSERM UMR-S 1258 / CNRS UMR7104/ Université de Strasbourg, 1 rue Laurent Fries, 67400, Illkirch, France.
Brillet K; Institut Biologie Moléculaire et Cellulaire (IBMC), CNRS UPR9002, 2 allée Konrad Roentgen, 67000, Strasbourg, France.
Orfanoudakis G; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France.
Poterszman A; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) / INSERM UMR-S 1258 / CNRS UMR7104/ Université de Strasbourg, 1 rue Laurent Fries, 67400, Illkirch, France.
Torbeev V; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France.
Rappsilber J; Institute of Biotechnology, Technische Universität Berlin, Gustav-Meyer-Allee 25, Berlin, Germany.
Davey NE; Division of Cancer Biology, The Institute of Cancer Research, 237 Fulham Road, London, SW3 6JB, UK.
Chariot A; Laboratory of Cancer Biology, GIGA Cancer, University of Liege, CHU, Sart-Tilman, 4000, Liege, Belgium.; WELBIO department, WEL Research Institute, avenue Pasteur, 6, 1300, Wavre, Belgium.
Zanier K; Biotechnology and Cell Signaling (CNRS/Université de Strasbourg, UMR7242), Ecole Superieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, 67400, Illkirch, France. .; Pokaż więcej
Źródło:: Nature communications [Nat Commun] 2024 Sep 03; Vol. 15 (1), pp. 7692. Date of Electronic Publication: 2024 Sep 03.
Typ publikacji:: Journal Article
MeSH Terms:: I-kappa B Kinase*/metabolism
I-kappa B Kinase*/chemistry
I-kappa B Kinase*/genetics
NF-kappa B*/metabolism
Protein Multimerization*
Amino Acid Motifs*
Humans ; Phosphorylation ; Protein Binding ; Signal Transduction ; NF-KappaB Inhibitor alpha/metabolism ; NF-KappaB Inhibitor alpha/genetics ; Molecular Docking Simulation ; HEK293 Cells ; Substrate Specificity

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Tytuł:: Citrullination modulation stabilizes HIF-1α to promote tumour progression.
Autorzy:: Chen R; School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, China.
Lin Z; School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, China.
Shen S; Medical Research Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, China.
Zhu C; School of Medicine, South China University of Technology, Guangzhou, China.
Yan K; Medical Research Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, China.
Suo C; Department of Colorectal Surgery, Guangzhou First People's Hospital, South China University of Technology, Guangzhou, China.
Liu R; The CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Basic Medical Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Wei H; Medical Research Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, China.
Gao L; School of Medicine, South China University of Technology, Guangzhou, China.
Fan K; School of Medicine, South China University of Technology, Guangzhou, China.
Zhang H; The CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Basic Medical Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Sun L; Medical Research Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, China. .
Gao P; School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou, China. .; Medical Research Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, China. .; Pokaż więcej
Źródło:: Nature communications [Nat Commun] 2024 Sep 03; Vol. 15 (1), pp. 7654. Date of Electronic Publication: 2024 Sep 03.
Typ publikacji:: Journal Article
MeSH Terms:: Hypoxia-Inducible Factor 1, alpha Subunit*/metabolism
Hypoxia-Inducible Factor 1, alpha Subunit*/genetics
Protein-Arginine Deiminase Type 4*/metabolism
Citrullination*
Liver Neoplasms*/metabolism
Liver Neoplasms*/pathology
Liver Neoplasms*/genetics
Disease Progression*
Carcinoma, Hepatocellular*/metabolism
Carcinoma, Hepatocellular*/pathology
Carcinoma, Hepatocellular*/genetics
Humans ; Animals ; Cell Line, Tumor ; Ubiquitination ; Von Hippel-Lindau Tumor Suppressor Protein/metabolism ; Von Hippel-Lindau Tumor Suppressor Protein/genetics ; Mice ; HEK293 Cells ; Protein Stability/drug effects ; Protein-Arginine Deiminases/metabolism ; Protein-Arginine Deiminases/genetics ; Mice, Nude ; Male

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Tytuł:: A molecular mechanism to diversify Ca signaling downstream of Gs protein-coupled receptors.
Autorzy:: Brands J; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.; Research Training Group 1873, University of Bonn, Bonn, Germany.
Bravo S; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.
Jürgenliemke L; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.; Research Training Group 2873, University of Bonn, Bonn, Germany.
Grätz L; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Schihada H; Department of Pharmaceutical Chemistry, Philipps-University Marburg, Marburg, Germany.
Frechen F; Institute of Innate Immunity, Medical Faculty, University of Bonn, Bonn, Germany.
Alenfelder J; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.
Pfeil C; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.; Research Training Group 1873, University of Bonn, Bonn, Germany.; Amsterdam Institute for Molecular and Life Sciences (AIMMS), Division of Medicinal Chemistry, Faculty of Science, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Ohse PG; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.
Hiratsuka S; Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, 980-8578, Japan.
Kawakami K; Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, 980-8578, Japan.; Komaba Institute for Science, The University of Tokyo, Meguro, Tokyo, 153-8505, Japan.
Schmacke LC; Department of Pharmaceutical Chemistry, Philipps-University Marburg, Marburg, Germany.
Heycke N; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.
Inoue A; Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, 980-8578, Japan.; Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, 606-8501, Japan.
König G; Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.
Pfeifer A; Institute of Pharmacology and Toxicology, University Hospital, University of Bonn, Bonn, Germany.
Wachten D; Institute of Innate Immunity, Medical Faculty, University of Bonn, Bonn, Germany.
Schulte G; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Steinmetzer T; Department of Pharmaceutical Chemistry, Philipps-University Marburg, Marburg, Germany.
Watts VJ; Department of Medicinal Chemistry and Molecular Pharmacology, Purdue Institute of Drug Discovery, Purdue University, West Lafayette, IN, USA.
Gomeza J; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.
Simon K; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany.; Department of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131, Padova, Italy.
Kostenis E; Molecular, Cellular and Pharmacobiology Section, Institute for Pharmaceutical Biology, University of Bonn, Bonn, Germany. .; Pokaż więcej
Źródło:: Nature communications [Nat Commun] 2024 Sep 03; Vol. 15 (1), pp. 7684. Date of Electronic Publication: 2024 Sep 03.
Typ publikacji:: Journal Article
MeSH Terms:: Calcium Signaling*
Phospholipase C beta*/metabolism
Phospholipase C beta*/genetics
Receptors, G-Protein-Coupled*/metabolism
Receptors, G-Protein-Coupled*/genetics
Calcium*/metabolism
Humans ; HEK293 Cells ; GTP-Binding Protein alpha Subunits, Gq-G11/metabolism ; GTP-Binding Protein alpha Subunits, Gq-G11/genetics ; CRISPR-Cas Systems ; GTP-Binding Protein alpha Subunits, Gs/metabolism ; GTP-Binding Protein alpha Subunits, Gs/genetics ; Cyclic AMP/metabolism ; Animals ; Gene Editing ; Cytosol/metabolism ; GTP-Binding Protein beta Subunits/metabolism ; GTP-Binding Protein beta Subunits/genetics ; Adenylyl Cyclases/metabolism ; Adenylyl Cyclases/genetics

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Tytuł:: Poly-GR Impairs PRMT1-Mediated Arginine Methylation of Disease-Linked RNA-Binding Proteins by Acting as a Substrate Sink.
Autorzy:: Hutten S; Institute of Molecular Physiology, Johannes Gutenberg-Universität, 55128 Mainz, Germany.
Chen JX; Institute of Molecular Biology, 55128 Mainz, Germany.
Isaacs AM; UK Dementia Research Institute at UCL, London WC1E 6BT, U.K.; Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, London WC1N 3BG, U.K.
Dormann D; Institute of Molecular Physiology, Johannes Gutenberg-Universität, 55128 Mainz, Germany.; Institute of Molecular Biology, 55128 Mainz, Germany.; Pokaż więcej
Źródło:: Biochemistry [Biochemistry] 2024 Sep 03; Vol. 63 (17), pp. 2141-2152. Date of Electronic Publication: 2024 Aug 15.
Typ publikacji:: Journal Article
MeSH Terms:: Protein-Arginine N-Methyltransferases*/metabolism
Protein-Arginine N-Methyltransferases*/genetics
Arginine*/metabolism
Repressor Proteins*/metabolism
Repressor Proteins*/genetics
RNA-Binding Proteins*/metabolism
RNA-Binding Proteins*/genetics
Humans ; Methylation ; Amyotrophic Lateral Sclerosis/metabolism ; Amyotrophic Lateral Sclerosis/genetics ; Frontotemporal Dementia/metabolism ; Frontotemporal Dementia/genetics ; C9orf72 Protein/metabolism ; C9orf72 Protein/genetics ; HEK293 Cells

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Tytuł:: Marburg virus exploits the Rab11-mediated endocytic pathway in viral-particle production.
Autorzy:: Furuyama W; National Research Center for the Control and Prevention of Infectious Diseases, Nagasaki University, Nagasaki, Japan.
Yamada K; National Research Center for the Control and Prevention of Infectious Diseases, Nagasaki University, Nagasaki, Japan.
Sakaguchi M; Central Laboratory, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.
Marzi A; Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA.
Nanbo A; National Research Center for the Control and Prevention of Infectious Diseases, Nagasaki University, Nagasaki, Japan.; Pokaż więcej
Źródło:: Microbiology spectrum [Microbiol Spectr] 2024 Sep 03; Vol. 12 (9), pp. e0026924. Date of Electronic Publication: 2024 Jul 30.
Typ publikacji:: Journal Article
MeSH Terms:: rab GTP-Binding Proteins*/metabolism
rab GTP-Binding Proteins*/genetics
Marburgvirus*/physiology
Marburgvirus*/genetics
Marburgvirus*/metabolism
Viral Matrix Proteins*/metabolism
Viral Matrix Proteins*/genetics
Endocytosis*
Virion*/metabolism
Humans ; Animals ; Microtubules/metabolism ; Microtubules/virology ; Virus Release ; Cell Line ; HEK293 Cells ; Virus Replication

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Tytuł:: SLC7A11-mediated cystine import protects against NDUFS7 deficiency-induced cell death in HEK293T cells.
Autorzy:: Chen J; Clinical Research Center, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Gao L; Department of Obstetrics and Gynecology, Zhujiang Hospital, Southern Medical University, Guangzhou, China. Electronic address: .; Pokaż więcej
Źródło:: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2024 Sep 03; Vol. 723, pp. 150178. Date of Electronic Publication: 2024 May 29.
Typ publikacji:: Journal Article
MeSH Terms:: Amino Acid Transport System y+*/metabolism
Amino Acid Transport System y+*/genetics
Cystine*/metabolism
Electron Transport Complex I*/metabolism
Electron Transport Complex I*/genetics
Electron Transport Complex I*/deficiency
Humans ; Apoptosis ; Cell Death ; Glutathione/metabolism ; HEK293 Cells ; Oxidative Stress ; Reactive Oxygen Species/metabolism

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Tytuł:: Crosstalk between PKA and PIAS3 regulates cardiac Kv4 channel SUMOylation.
Autorzy:: Jansen LR; Department of Biology, Georgia State University, Atlanta, GA, USA.
Welch MA; Department of Biology, Georgia State University, Atlanta, GA, USA.; Present Address: Section on Molecular Neurophysiology and Biophysics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA.
Plant LD; Department of Pharmaceutical Sciences, Center for Drug Discovery, Northeastern University, Boston, MA, USA.
Baro DJ; Department of Biology, Georgia State University, Atlanta, GA, USA. .; Pokaż więcej
Źródło:: Cell communication and signaling : CCS [Cell Commun Signal] 2024 Sep 02; Vol. 22 (1), pp. 422. Date of Electronic Publication: 2024 Sep 02.
Typ publikacji:: Journal Article
MeSH Terms:: Sumoylation*
Cyclic AMP-Dependent Protein Kinases*/metabolism
Protein Inhibitors of Activated STAT*/metabolism
Protein Inhibitors of Activated STAT*/genetics
Myocytes, Cardiac*/metabolism
Shal Potassium Channels*/metabolism
Shal Potassium Channels*/genetics
Humans ; HEK293 Cells ; Animals ; Phosphorylation ; Molecular Chaperones/metabolism ; Molecular Chaperones/genetics

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Tytuł:: The mTOR pathway controls phosphorylation of BRAF at T401.
Autorzy:: Christen D; Institute of Molecular Medicine, University of Freiburg, Stefan-Meier-Str. 17, 79104, Freiburg, Germany.; Faculty of Biology, University of Freiburg, Freiburg, Germany.; German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Partner Site Freiburg and, Heidelberg, 69120, Germany.
Lauinger M; Institute of Molecular Medicine, University of Freiburg, Stefan-Meier-Str. 17, 79104, Freiburg, Germany.; Faculty of Biology, University of Freiburg, Freiburg, Germany.
Brunner M; Department of Biology, University of Fribourg, Chemin du Museé 10, 1700, Fribourg, Switzerland.
Dengjel J; Department of Biology, University of Fribourg, Chemin du Museé 10, 1700, Fribourg, Switzerland.
Brummer T; Institute of Molecular Medicine, University of Freiburg, Stefan-Meier-Str. 17, 79104, Freiburg, Germany. .; German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Partner Site Freiburg and, Heidelberg, 69120, Germany. .; Comprehensive Cancer Center Freiburg (CCCF), Medical Center, Faculty of Medicine, University of Freiburg, University of Freiburg, 79106, Freiburg, Germany. .; Center for Biological Signalling Studies BIOSS, University of Freiburg, 79104, Freiburg, Germany. .; Pokaż więcej
Źródło:: Cell communication and signaling : CCS [Cell Commun Signal] 2024 Sep 02; Vol. 22 (1), pp. 428. Date of Electronic Publication: 2024 Sep 02.
Typ publikacji:: Journal Article
MeSH Terms:: TOR Serine-Threonine Kinases*/metabolism
Proto-Oncogene Proteins B-raf*/metabolism
Proto-Oncogene Proteins B-raf*/genetics
Phosphorylation/drug effects ; Humans ; Animals ; Mice ; Signal Transduction/drug effects ; HEK293 Cells ; Pyrimidinones/pharmacology ; Mechanistic Target of Rapamycin Complex 1/metabolism ; Pyridones/pharmacology ; Naphthyridines

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