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伴侣介导的自噬机制。

Mechanisms of chaperone-mediated autophagy.

作者信息

Majeski Amy E, Dice J Fred

机构信息

Department of Physiology, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111, USA.

出版信息

Int J Biochem Cell Biol. 2004 Dec;36(12):2435-44. doi: 10.1016/j.biocel.2004.02.013.

Abstract

Chaperone-mediated autophagy is one of several lysosomal pathways of proteolysis. This pathway is activated by physiological stresses such as prolonged starvation. Cytosolic proteins with particular peptide sequence motifs are recognized by a complex of molecular chaperones and delivered to lysosomes. No vesicular traffic is required for this protein degradation pathway, so it differs from microautophagy and macroautophagy. Protein substrates bind to a receptor in the lysosomal membrane, the lysosome-associated membrane protein (lamp) type 2a. Levels of lamp2a in the lysosomal membrane are controlled by alterations in the lamp2a half-life as well as by the dynamic distribution of the protein between the lysosomal membrane and the lumen. Substrate proteins are unfolded before transport into the lysosome lumen, and the transport of substrate proteins requires a molecular chaperone within the lysosomal lumen. The exact roles of this lysosomal chaperone remain to be defined. The mechanisms of chaperone-mediated autophagy are similar to mechanisms of protein import into mitochondria, chloroplasts, and the endoplasmic reticulum.

摘要

伴侣蛋白介导的自噬是几种溶酶体蛋白水解途径之一。该途径由长时间饥饿等生理应激激活。具有特定肽序列基序的胞质蛋白被分子伴侣复合物识别并输送到溶酶体。这种蛋白质降解途径不需要囊泡运输,因此它不同于微自噬和巨自噬。蛋白质底物与溶酶体膜中的一种受体,即2a型溶酶体相关膜蛋白(lamp)结合。溶酶体膜中lamp2a的水平受lamp2a半衰期的变化以及该蛋白在溶酶体膜和腔之间的动态分布控制。底物蛋白在转运到溶酶体腔之前会发生解折叠,底物蛋白的转运需要溶酶体腔内的分子伴侣。这种溶酶体伴侣的确切作用仍有待确定。伴侣蛋白介导的自噬机制类似于蛋白质导入线粒体、叶绿体和内质网的机制。

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