Artificial Metal–Peptide Assemblies: Bioinspired Assembly of Peptides and Metals through Space and across Length Scales

纳米技术 化学 生物分子 金属有机骨架 组合化学 金属 材料科学 有机化学 生物化学 吸附
作者
Jinqiao Dong,Yan Liu,Yong Cui
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:143 (42): 17316-17336 被引量:67
标识
DOI:10.1021/jacs.1c08487
摘要

The exploration of chiral crystalline porous materials, such as metal-organic complexes (MOCs) or metal-organic frameworks (MOFs), has been one of the most exciting recent developments in materials science owing to their widespread applications in enantiospecific processes. However, achieving specific tight-affinity binding and remarkable enantioselectivity toward important biomolecules is still challenging. Perhaps most critically, the lack of adaptability, compatibility, and processability in these materials severely impedes practical applications in chemical engineering and biological technology. In this Perspective, artificial metal-peptide assemblies (MPAs), which are achieved by the assembly of peptides and metals with nanometer-sized cavities or pores, is a new development that could address the current bottlenecks of chiral porous materials. Bioinspired assembly of pore-forming MPAs is not foreign to biological systems and has granted scientists an unprecedented level of control over the chiral recognition sites, conformational flexibility, cavity sizes, and hydrophilic segments through ultrafine-tuning of peptide-derived linkers. We will specifically discuss exemplary MPAs including structurally well-defined metal-peptide complexes and highly crystalline metal-peptide frameworks. With insights from these structures, the peptide assembly and folding by the closer cooperation of metal coordination and noncovalent interactions can create adaptable protein-like nanocavities undergoing a myriad of conformational variations that is reminiscent of enzymatic pockets. We also consider challenges to advancing the field, where the deployment of side-chain groups and manipulation of amino acid sequences are more likely to access the programmable, genetically encodable peptide-mediated porous materials, thus contributing to the enhanced enantioselective recognition as well as enabling key biochemical processes in next-generation versatile biomimetic materials.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研通AI6.4应助mujin采纳,获得10
刚刚
1秒前
1秒前
快乐曼荷完成签到,获得积分10
2秒前
zjm完成签到,获得积分10
2秒前
2秒前
3秒前
3秒前
9秒前
Orange应助123采纳,获得30
10秒前
刻苦初翠发布了新的文献求助10
10秒前
平常母鸡完成签到,获得积分10
11秒前
桐桐应助明理的凡霜采纳,获得10
11秒前
fuguier完成签到,获得积分10
12秒前
12秒前
清脆如风发布了新的文献求助10
12秒前
白冷之完成签到,获得积分10
12秒前
17秒前
111关闭了111文献求助
19秒前
20秒前
白鹭思一骋给不爱吃饭的求助进行了留言
22秒前
22秒前
Lucas应助SXR采纳,获得10
25秒前
Jamesliu完成签到,获得积分10
26秒前
流觞完成签到 ,获得积分10
27秒前
123发布了新的文献求助30
27秒前
初景发布了新的文献求助30
27秒前
外向山雁完成签到,获得积分10
28秒前
多金多金完成签到,获得积分10
29秒前
科研通AI6.4应助无尽夏采纳,获得10
30秒前
小马甲应助刻苦初翠采纳,获得10
31秒前
33秒前
纯情的雨雪完成签到,获得积分10
33秒前
35秒前
Copyright应助激昂的眼神采纳,获得10
36秒前
一羊完成签到,获得积分10
36秒前
36秒前
37秒前
冯大哥完成签到,获得积分10
38秒前
刻苦初翠完成签到,获得积分20
39秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7265486
求助须知:如何正确求助?哪些是违规求助? 8886465
关于积分的说明 18781768
捐赠科研通 6943091
什么是DOI,文献DOI怎么找? 3202907
关于科研通互助平台的介绍 2376043
邀请新用户注册赠送积分活动 2178820