Chemical tools for understanding protein lipidation in eukaryotes

被引:52
作者
Charron, Guillaume [1 ]
Wilson, John [1 ]
Hang, Howard C. [1 ]
机构
[1] Rockefeller Univ, Lab Chem Biol & Microbial Pathogenesis, New York, NY 10065 USA
关键词
GDP-DISSOCIATION INHIBITOR; N-MYRISTOYL TRANSFERASE; IN-VITRO; FARNESYL DIPHOSPHATE; ANCHORED PROTEINS; MAMMALIAN-CELLS; RAPID DETECTION; WNT PROTEIN; FATTY-ACIDS; PALMITOYLATION;
D O I
10.1016/j.cbpa.2009.07.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipidation of proteins is an important mechanism to regulate protein trafficking and activity in cell and tissues. The targeting of proteins to membranes by lipidation plays key roles in many physiological processes and when not regulated properly can lead to cancer and neurological disorders. Dissecting the precise roles of protein lipidation in physiology and disease is a major challenge. Recent advances in chemical biology have now enabled the semisynthesis of lipidated proteins for fundamental biochemical and cellular studies. In addition, new chemical reporters of protein lipidation have improved the detection and enabled the proteomic analysis of lipidated proteins. The expanding efforts in chemical biology are therefore providing new tools to dissect the mechanisms and functions of protein lipidation as well as develop therapeutics targeted at protein lipidation pathways in disease.
引用
收藏
页码:382 / 391
页数:10
相关论文
共 67 条
[61]   Inhibition of protein palmitoylation, raft localization, and T cell signaling by 2-bromopalmitate and polyunsaturated fatty acids [J].
Webb, Y ;
Hermida-Matsumoto, L ;
Resh, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (01) :261-270
[62]   Influence of the Lipidation Motif on the Partitioning and Association of N-Ras in Model Membrane Subdomains [J].
Weise, Katrin ;
Triola, Gemma ;
Brunsveld, Luc ;
Waldmann, Herbert ;
Winter, Roland .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (04) :1557-1564
[63]   K- and N-Ras are geranylgeranylated in cells treated with farnesyl protein transferase inhibitors [J].
Whyte, DB ;
Kirschmeier, P ;
Hockenberry, TN ;
NunezOliva, I ;
James, L ;
Catino, JJ ;
Bishop, WR ;
Pai, JK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (22) :14459-14464
[64]   Interaction analysis of prenylated Rab GTPase with Rab escort protein and GDP dissociation inhibitor explains the need for both regulators [J].
Wu, Yao-Wen ;
Tan, Kui-Thong ;
Waldmann, Herbert ;
Goody, Roger S. ;
Alexandrov, Kirill .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (30) :12294-12299
[65]   A protein fluorescence amplifier: Continuous fluorometric assay for Rab geranylgeranyltransferase [J].
Wu, Yao-Wen ;
Waldmann, Herbert ;
Reents, Reinhard ;
Ebetino, Frank H. ;
Goody, Roger S. ;
Alexandrova, Kirill .
CHEMBIOCHEM, 2006, 7 (12) :1859-1861
[66]   Posttranslational N-myristoylation of BID as a molecular switch for targeting mitochondria and apoptosis [J].
Zha, JP ;
Weiler, S ;
Oh, KJ ;
Wei, MC ;
Korsmeyer, SJ .
SCIENCE, 2000, 290 (5497) :1761-1765
[67]   Identification of CKAP4/p63 as a major substrate of the palmitoyl acyltransferase DHHC2, a putative tumor suppressor, using a novel proteomics method [J].
Zhang, Jun ;
Planey, Sonia L. ;
Ceballos, Carolina ;
Stevens, Stanley M., Jr. ;
Keay, Susan K. ;
Zacharias, David A. .
MOLECULAR & CELLULAR PROTEOMICS, 2008, 7 (07) :1378-1388