4.5 Review

Global profiling of protein lipidation using chemical proteomic technologies

期刊

CURRENT OPINION IN CHEMICAL BIOLOGY
卷 24, 期 -, 页码 48-57

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.cbpa.2014.10.016

关键词

-

资金

  1. Biotechnology and Biological Sciences Research Council [BB/D02014X/1]
  2. European Commission's Research Executive Agency (ProbesPTRM)
  3. Cancer Research UK [C6433/A16402, C29637/A10711]
  4. British Heart Foundation
  5. BBSRC [BB/D02014X/1] Funding Source: UKRI
  6. MRC [G0502214] Funding Source: UKRI
  7. Biotechnology and Biological Sciences Research Council [BB/D02014X/1] Funding Source: researchfish
  8. Cancer Research UK [20183] Funding Source: researchfish
  9. Medical Research Council [G0502214] Funding Source: researchfish

向作者/读者索取更多资源

Protein lipidation is unique amongst post-translational modifications (PTMs) in enabling direct interaction with cell membranes, and is found in every form of life. Lipidation is important in normal function and in disease, but its intricate interplay with disease context presents a challenging for drug development. Global whole-proteome profiling of protein lipidation lies beyond the range of standard methods, but is well-suited to metabolic tagging with small 'clickable' chemical reporters that do not disrupt metabolism and function; chemoselective reactions are then used to add multifunctional labels exclusively to tagged-lipidated proteins. This chemical proteomic technology has opened up the first quantitative whole-proteome studies of the known major classes of protein lipidation, and the first insights into their full scope in vivo.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据