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真核生物中通过共翻译折叠促进蛋白质结构域的重组。

Recombination of protein domains facilitated by co-translational folding in eukaryotes.

作者信息

Netzer W J, Hartl F U

机构信息

Cellular Biochemistry & Biophysics Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.

出版信息

Nature. 1997 Jul 24;388(6640):343-9. doi: 10.1038/41024.

Abstract

The evolution of complex genomes requires that new combinations of pre-existing protein domains successfully fold into modular polypeptides. During eukaryotic translation model two-domain polypeptides fold efficiently by sequential and co-translational folding of their domains. In contrast, folding of the same proteins in Escherichia coli is posttranslational, and leads to intramolecular misfolding of concurrently folding domains. Sequential domain folding in eukaryotes may have been critical in the evolution of modular polypeptides, by increasing the probability that random gene-fusion events resulted in immediately foldable protein structures.

摘要

复杂基因组的进化要求预先存在的蛋白质结构域的新组合能够成功折叠成模块化多肽。在真核生物翻译过程中,双结构域多肽通过其结构域的顺序和共翻译折叠而有效折叠。相比之下,相同的蛋白质在大肠杆菌中是翻译后折叠的,这会导致同时折叠的结构域发生分子内错误折叠。真核生物中结构域的顺序折叠可能在模块化多肽的进化中至关重要,因为它增加了随机基因融合事件产生可立即折叠的蛋白质结构的可能性。

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