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蛋白质从头设计中的模板

Templates in protein de novo design.

作者信息

Tuchscherer G, Mutter M

机构信息

Institute of Organic Chemistry, University of Lausanne, Switzerland.

出版信息

J Biotechnol. 1995 Jul 31;41(2-3):197-210. doi: 10.1016/0168-1656(95)00010-n.

Abstract

The de novo design of polypeptide sequences with a three-dimensional structure necessary for many biological functions is limited by the complex folding process, or 'protein folding problem'. This problem can be bypassed through constructing protein-like molecules with a 'built-in' device for intramolecular folding, that is, proteins of non-natural chain architecture (template-assembled synthetic proteins, TASP). Topological templates have become a versatile tool for inducing and stabilizing secondary structures (protein loops, beta-turns, alpha-helices, beta-sheets) and are widely adopted design elements for the construction of protein-like molecules, exhibiting interesting structural and functional properties.

摘要

具有许多生物学功能所必需的三维结构的多肽序列的从头设计受到复杂折叠过程(即“蛋白质折叠问题”)的限制。通过构建具有分子内折叠“内置”装置的类蛋白质分子,即非天然链结构的蛋白质(模板组装合成蛋白,TASP),可以绕过这个问题。拓扑模板已成为诱导和稳定二级结构(蛋白质环、β-转角、α-螺旋、β-折叠)的通用工具,并且是构建类蛋白质分子广泛采用的设计元素,展现出有趣的结构和功能特性。

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