How many lives does CLIMP-63 have?

被引:23
|
作者
Sandoz, Patrick A. [1 ]
van der Goot, F. Gisou [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Global Hlth Inst, CH-1015 Lausanne, Switzerland
基金
欧洲研究理事会;
关键词
cytoskeleton-linking membrane protein (CLIMP-63)/cytoskeleton-associated protein 4 (CKAP4); palmitoyl-acyltransferase 2 (has a DHHC motif) [DHHC2; endoplasmic reticulum (ER) cytoskeleton anchor; nuclear translocation; palmitoylation; plasma membrane receptor; rough endoplasmic reticulum (RER); PALMITOYL ACYLTRANSFERASE DHHC2; GOLGI INTERMEDIATE COMPARTMENT; ENDOPLASMIC-RETICULUM; ANTIPROLIFERATIVE FACTOR; MEMBRANE-PROTEIN; P63; CKAP4; EXPRESSION; MICROTUBULES; ORGANIZATION; CARCINOMA;
D O I
10.1042/BST20140272
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
In 1995, in the Biochemical Society Transactions, Mundy published the first review on CLIMP-63 (cytoskeletonlinking membrane protein 63) or CKPA4 (cytoskeleton-associated protein 4), initially just p63 [1]. Here we review the following 20 years of research on this stillmysterious protein. CLIMP-63 is a type II transmembrane protein, the cytosolic domain of which has the capacity to bind microtubules whereas the luminal domain can form homo-oligomeric complexes, not only with neighbouring molecules but also, in trans, with CLIMP-63 molecules on the other side of the endoplasmic reticulum (ER) lumen, thus promoting the formation of ER sheets. CLIMP-63 however also appears to have a life at the cell surface where it acts as a ligand-activated receptor. The still rudimentary information of how CLIMP-63 fulfills these different roles, what these are exactly and how post-translational modifications control them, will be discussed.
引用
收藏
页码:222 / 228
页数:7
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