School of Physics, University of New South Wales, Sydney, NSW 2052, Australia.
FEBS Lett. 2010 May 17;584(10):2093-101. doi: 10.1016/j.febslet.2010.01.027. Epub 2010 Jan 19.
Chloride intracellular channel proteins (CLICs) are distinct from most ion channels in that they have both soluble and integral membrane forms. CLICs are highly conserved in chordates, with six vertebrate paralogues. CLIC-like proteins are found in other metazoans. CLICs form channels in artificial bilayers in a process favoured by oxidising conditions and low pH. They are structurally plastic, with CLIC1 adopting two distinct soluble conformations. Phylogenetic and structural data indicate that CLICs are likely to have enzymatic function. The physiological role of CLICs appears to be maintenance of intracellular membranes, which is associated with tubulogenesis but may involve other substructures.
氯离子细胞内通道蛋白(CLICs)与大多数离子通道不同,它们既有可溶性形式,也有整合膜形式。CLICs 在脊索动物中高度保守,有六个脊椎动物的同源物。类似 CLIC 的蛋白在其他后生动物中也有发现。CLIC 蛋白在人工双层膜中形成通道,这一过程受到氧化条件和低 pH 值的促进。它们结构具有可塑性,CLIC1 采用两种不同的可溶性构象。系统发生和结构数据表明,CLIC 可能具有酶的功能。CLIC 的生理作用似乎是维持细胞内膜,这与小管形成有关,但可能涉及其他亚结构。