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Tytuł pozycji:

Surfactant-assisted one-pot sample preparation for label-free single-cell proteomics.

Tytuł:
Surfactant-assisted one-pot sample preparation for label-free single-cell proteomics.
Autorzy:
Tsai CF; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Zhang P; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.; NHC Key Laboratory of Cancer Proteomics, Department of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, P.R. China.
Scholten D; Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Martin K; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Wang YT; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Zhao R; Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, USA.
Chrisler WB; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Patel DB; Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Dou M; Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, USA.
Jia Y; Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Reduzzi C; Division of Hematology and Oncology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Liu X; Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Moore RJ; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Burnum-Johnson KE; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Lin MH; Graduate Institute of Microbiology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Hsu CC; Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
Jacobs JM; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Kagan J; Cancer Biomarkers Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD, USA.
Srivastava S; Cancer Biomarkers Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD, USA.
Rodland KD; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Steven Wiley H; Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, USA.
Qian WJ; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Smith RD; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA.
Zhu Y; Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, USA.
Cristofanilli M; Division of Hematology and Oncology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.; Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Liu T; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA. .
Liu H; Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. .; Division of Hematology and Oncology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. .; Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. .
Shi T; Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, USA. .
Źródło:
Communications biology [Commun Biol] 2021 Mar 01; Vol. 4 (1), pp. 265. Date of Electronic Publication: 2021 Mar 01.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
Język:
English
Imprint Name(s):
Original Publication: London, United Kingdom : Nature Publishing Group UK, [2018]-
MeSH Terms:
Proteome*
Proteomics*
Single-Cell Analysis*
Breast Neoplasms/*metabolism
Glucosides/*chemistry
Lung Neoplasms/*metabolism
Neoplasm Proteins/*metabolism
Neoplastic Cells, Circulating/*metabolism
Surface-Active Agents/*chemistry
Animals ; Breast Neoplasms/pathology ; Chromatography, Liquid ; Female ; Humans ; Lung Neoplasms/secondary ; MCF-7 Cells ; Mice ; Neoplasm Micrometastasis ; Neoplastic Cells, Circulating/pathology ; Spectrometry, Mass, Electrospray Ionization ; Tandem Mass Spectrometry
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Grant Information:
P41 GM103493 United States GM NIGMS NIH HHS; T32 CA009560 United States CA NCI NIH HHS; UG3 CA256967 United States CA NCI NIH HHS; R01 CA245699 United States CA NCI NIH HHS; R01 DK122160 United States DK NIDDK NIH HHS; R21 CA223715 United States CA NCI NIH HHS; UL1 TR001422 United States TR NCATS NIH HHS; U24 CA210955 United States CA NCI NIH HHS; UH3 CA256967 United States CA NCI NIH HHS; U01 CA227544 United States CA NCI NIH HHS
Substance Nomenclature:
0 (Glucosides)
0 (Neoplasm Proteins)
0 (Proteome)
0 (Surface-Active Agents)
69227-93-6 (dodecyl maltoside)
Entry Date(s):
Date Created: 20210302 Date Completed: 20210810 Latest Revision: 20230701
Update Code:
20240105
PubMed Central ID:
PMC7921383
DOI:
10.1038/s42003-021-01797-9
PMID:
33649493
Czasopismo naukowe
Large numbers of cells are generally required for quantitative global proteome profiling due to surface adsorption losses associated with sample processing. Such bulk measurement obscures important cell-to-cell variability (cell heterogeneity) and makes proteomic profiling impossible for rare cell populations (e.g., circulating tumor cells (CTCs)). Here we report a surfactant-assisted one-pot sample preparation coupled with mass spectrometry (MS) method termed SOP-MS for label-free global single-cell proteomics. SOP-MS capitalizes on the combination of a MS-compatible nonionic surfactant, n-Dodecyl-β-D-maltoside, and hydrophobic surface-based low-bind tubes or multi-well plates for 'all-in-one' one-pot sample preparation. This 'all-in-one' method including elimination of all sample transfer steps maximally reduces surface adsorption losses for effective processing of single cells, thus improving detection sensitivity for single-cell proteomics. This method allows convenient label-free quantification of hundreds of proteins from single human cells and ~1200 proteins from small tissue sections (close to ~20 cells). When applied to a patient CTC-derived xenograft (PCDX) model at the single-cell resolution, SOP-MS can reveal distinct protein signatures between primary tumor cells and early metastatic lung cells, which are related to the selection pressure of anti-tumor immunity during breast cancer metastasis. The approach paves the way for routine, precise, quantitative single-cell proteomics.
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