期刊
JOURNAL OF PROTEOME RESEARCH
卷 8, 期 5, 页码 2140-2143出版社
AMER CHEMICAL SOC
DOI: 10.1021/pr8009879
关键词
quantitative proteomics; isotope labeling; clinical proteomics; (18)O-labeling; absolute quantitation; tissue proteomics; plasma proteome; biofilms; mitochondria; plasma membrane; formalin-fixed paraffin; laser capture micro-dissection; affinity fractionation; protein cross-linking; glycoproteins
Enzyme-catalyzed (18)O(2)-labeling offers a universal strategy for uniform labeling of all peptides from any kind of proteins, including post-translationally modified proteins. It is applicable to clinical samples with unrivaled sensitivity. This review discusses strengths and limitations, and advocates the separation of proteolysis from the labeling step. Continued advances in software will facilitate widespread use of enzyme-catalyzed (18)O(2)-labeling to determine changes in protein abundances.
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