光致多肽材料:自组装和生物功能的时空控制

IF 2.9 Q2 BIOPHYSICS
K. Matsuura, H. Inaba
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引用次数: 0

摘要

肽既可以作为调节各种生物现象的功能分子,也可以作为自组装人工材料。在肽中引入光致伸缩单元,可以在光照射下对肽的结构和功能进行时空遥控。本文概述了过去 30 年中光致多肽的设计、与生物分子的相互作用以及在自组装材料中的应用。用偶氮苯和螺吡喃等光致变色(可光异构)分子修饰的肽,可逆地通过光控与生物大分子结合,并通过自组装形成纳米结构。可光裂解分子单元通过主链的裂解和光的脱保护作用,不可逆地控制肽的功能。肽与肽之间或肽与其他生物大分子之间的光交联增强了肽集合体和复合物的结构稳定性。通过适当的光照射,这些光致肽可时空控制肽集合体的形成和解离、基因表达、蛋白质-药物相互作用、蛋白质-蛋白质相互作用、脂质体变形和运动、细胞骨架结构和稳定性以及细胞功能。这些分子系统可应用于光控生物功能、分子机器人、人工细胞和新一代智能给药材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photoresponsive peptide materials: Spatiotemporal control of self-assembly and biological functions
Peptides work as both functional molecules to modulate various biological phenomena and self-assembling artificial materials. The introduction of photoresponsive units to peptides allows the spatiotemporal remote control of their structure and function upon light irradiation. This article overviews the photoresponsive peptide design, interaction with biomolecules, and applications in self-assembling materials over the last 30 years. Peptides modified with photochromic (photoisomerizable) molecules, such as azobenzene and spiropyran, reversibly photo-controlled the binding to biomolecules and nanostructure formation through self-assembly. Photocleavable molecular units irreversibly control the functions of peptides through cleavage of the main chain and deprotection by light. Photocrosslinking between peptides or between peptides and other biomolecules enhances the structural stability of peptide assemblies and complexes. These photoresponsive peptides spatiotemporally controlled the formation and dissociation of peptide assemblies, gene expressions, protein–drug interactions, protein–protein interactions, liposome deformation and motility, cytoskeleton structure and stability, and cell functions by appropriate light irradiation. These molecular systems can be applied to photo-control biological functions, molecular robots, artificial cells, and next-generation smart drug delivery materials.
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来源期刊
CiteScore
3.60
自引率
0.00%
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