Multimerisation of A disintegrin and metalloprotease protein-17 (ADAM17) is mediated by its EGF-like domain

被引：41
|
作者：
Lorenzen, Inken [1 ]
Trad, Ahmad [1 ]
Groetzinger, Joachim [1 ]
机构：
[1] Univ Kiel, Inst Biochem, D-24118 Kiel, Germany
来源：
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 2011年 / 415卷 / 02期
关键词：
ADAM; 17; Metalloprotease; Metzincins; EGF-like domain; Cysteine-rich domain; Multimerisation; Dimer; ALPHA-CONVERTING-ENZYME; NECROSIS-FACTOR-ALPHA; MOLECULAR SWITCH; INFLAMMATION; CELL;
D O I：
10.1016/j.bbrc.2011.10.056
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：
A disintegrin and metalloprotease protein 17 (ADAM17) is a transmembrane zinc dependent metalloprotease. The catalytic activity of the enzyme results in the shedding of a broad range of membrane proteins. The release of the corresponding ectodomains induces a switch in various physiological and pathophysiological processes. So far there is not much information about the molecular mechanism of ADAM 17 activation available. As for other transmembrane proteases, multimerisation may play a critical role in the activation and function of ADAM17. The present work demonstrates that ADAM17 indeed exists as a multimer in the cell membrane and that this multimerisation is mediated by its EGF-like domain. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码：330 / 336
页数：7
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