Truncation of the TPR domain of OGT alters substrate and glycosite selection.
Autorzy:
Ramirez DH; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.; Department of Plant Biology, Carnegie Institution for Science, Stanford, CA, USA. Yang B; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA. D'Souza AK; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA. Shen D; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA. WooCM; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA. .
Isotope-targeted glycoproteomics (IsoTaG) analysis of sialylated N- and O-glycopeptides on an Orbitrap Fusion Tribrid using azido and alkynyl sugars.
Autorzy:
WooCM; Department of Chemistry, Stanford University, Stanford, CA, 94305, USA. Felix A; Department of Chemistry, Stanford University, Stanford, CA, 94305, USA. Zhang L; Chemical and Systems Biology, Stanford University, Stanford, CA, 94305, USA. Elias JE; Chemical and Systems Biology, Stanford University, Stanford, CA, 94305, USA. Bertozzi CR; Department of Chemistry, Stanford University, Stanford, CA, 94305, USA. .; Howard Hughes Medical Institute, Stanford University, Stanford, CA, 94305, USA. .
Isotope-targeted glycoproteomics (IsoTaG): a mass-independent platform for intact N- and O-glycopeptide discovery and analysis.
Autorzy:
WooCM; Department of Chemistry, University of California, Berkeley, California, USA. Iavarone AT; QB3/Chemistry Mass Spectrometry Facility, University of California, Berkeley, California, USA. Spiciarich DR; Department of Chemistry, University of California, Berkeley, California, USA. Palaniappan KK; Department of Chemistry, University of California, Berkeley, California, USA. Bertozzi CR; 1] Department of Chemistry, University of California, Berkeley, California, USA. [2] Department of Molecular and Cell Biology, University of California, Berkeley, California, USA. [3] Howard Hughes Medical Institute, Berkeley, California, USA.
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Źródło:
Nature methods [Nat Methods] 2015 Jun; Vol. 12 (6), pp. 561-7. Date of Electronic Publication: 2015 Apr 20.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
The cytotoxicity of (-)-lomaiviticin A arises from induction of double-strand breaks in DNA.
Autorzy:
Colis LC; Department of Chemistry, Yale University, New Haven, Connecticut 06520, USA. WooCM; Department of Chemistry, Yale University, New Haven, Connecticut 06520, USA. Hegan DC; Departments of Therapeutic Radiology and Genetics, Yale School of Medicine, New Haven, Connecticut 06520, USA. Li Z; Department of Chemistry, Yale University, New Haven, Connecticut 06520, USA. Glazer PM; Departments of Therapeutic Radiology and Genetics, Yale School of Medicine, New Haven, Connecticut 06520, USA. Herzon SB; Department of Chemistry, Yale University, New Haven, Connecticut 06520, USA.
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Źródło:
Nature chemistry [Nat Chem] 2014 Jun; Vol. 6 (6), pp. 504-10. Date of Electronic Publication: 2014 May 11.
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.
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