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Co-assembly of aromatic dipeptides into spherical structures that are similar in morphology to red and white blood cells.芳香二肽共组装成形态与红细胞和白细胞相似的球形结构。
J Mater Chem B. 2014 May 7;2(17):2583-2591. doi: 10.1039/c3tb21456g. Epub 2014 Feb 4.
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Self-assembly of amphiphilic peptides into bio-functionalized nanotubes: a novel hydrolase model.两亲性肽自组装成生物功能化纳米管:一种新型水解酶模型。
J Mater Chem B. 2013 May 7;1(17):2297-2304. doi: 10.1039/c3tb20156b. Epub 2013 Mar 25.
3
Energy transfer within responsive pi-conjugated coassembled peptide-based nanostructures in aqueous environments.水性环境中基于响应性π共轭共组装肽的纳米结构内的能量转移。
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Self-assembling peptide semiconductors.自组装肽半导体
Science. 2017 Nov 17;358(6365). doi: 10.1126/science.aam9756.
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Molecular co-assembly as a strategy for synergistic improvement of the mechanical properties of hydrogels.分子共组装作为协同改善水凝胶力学性能的一种策略。
Chem Commun (Camb). 2017 Aug 24;53(69):9586-9589. doi: 10.1039/c7cc04187j.
6
Molecular, Local, and Network-Level Basis for the Enhanced Stiffness of Hydrogel Networks Formed from Coassembled Racemic Peptides: Predictions from Pauling and Corey.由外消旋肽共组装形成的水凝胶网络增强硬度的分子、局部和网络水平基础:来自鲍林和科里的预测。
ACS Cent Sci. 2017 Jun 28;3(6):586-597. doi: 10.1021/acscentsci.7b00115. Epub 2017 May 31.
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Fabrication of Supramolecular n/p-Nanowires via Coassembly of Oppositely Charged Peptide-Chromophore Systems in Aqueous Media.通过在水相中组装带相反电荷的肽-生色团体系来制备超分子 n/p-纳米线。
ACS Nano. 2017 Jul 25;11(7):6881-6892. doi: 10.1021/acsnano.7b02025. Epub 2017 Jul 11.
8
Kinetically Controlled Coassembly of Multichromophoric Peptide Hydrogelators and the Impacts on Energy Transport.动力学控制的多色荧光团肽凝胶因子的共组装及其对能量传递的影响。
J Am Chem Soc. 2017 Jun 28;139(25):8685-8692. doi: 10.1021/jacs.7b04006. Epub 2017 Jun 16.
9
Aromatic-Aromatic Interactions Enable α-Helix to β-Sheet Transition of Peptides to Form Supramolecular Hydrogels.芳香-芳香相互作用促使肽段从α-螺旋向β-折叠转变以形成超分子水凝胶。
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Disruption of diphenylalanine assembly by a Boc-modified variant.Boc 修饰变体对二苯丙氨酸组装的破坏。
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极简肽超分子共组装:拓展纳米技术的构象空间。

Minimalistic peptide supramolecular co-assembly: expanding the conformational space for nanotechnology.

机构信息

Department of Molecular Microbiology and Biotechnology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 6997801, Israel.

出版信息

Chem Soc Rev. 2018 May 21;47(10):3406-3420. doi: 10.1039/c7cs00827a.

DOI:10.1039/c7cs00827a
PMID:29498728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6338309/
Abstract

Molecular self-assembly is a ubiquitous process in nature and central to bottom-up nanotechnology. In particular, the organization of peptide building blocks into ordered supramolecular structures has gained much interest due to the unique properties of the products, including biocompatibility, chemical and structural diversity, robustness and ease of large-scale synthesis. In addition, peptides, as short as dipeptides, contain all the molecular information needed to spontaneously form well-ordered structures at both the nano- and the micro-scale. Therefore, peptide supramolecular assembly has been effectively utilized to produce novel materials with tailored properties for various applications in the fields of material science, engineering, medicine, and biology. To further expand the conformational space of peptide assemblies in terms of structural and functional complexity, multicomponent (two or more) peptide supramolecular co-assembly has recently evolved as a promising extended approach, similar to the structural diversity of natural sequence-defined biopolymers (proteins) as well as of synthetic covalent co-polymers. The use of this methodology was recently demonstrated in various applications, such as nanostructure physical dimension control, the creation of non-canonical complex topologies, mechanical strength modulation, the design of light harvesting soft materials, fabrication of electrically conducting devices, induced fluorescence, enzymatic catalysis and tissue engineering. In light of these significant advancements in the field of peptide supramolecular co-assembly in the last few years, in this tutorial review, we provide an updated overview and future prospects of this emerging subject.

摘要

分子自组装是自然界中普遍存在的过程,也是自下而上纳米技术的核心。特别是,由于产物具有独特的性能,包括生物相容性、化学和结构多样性、鲁棒性和易于大规模合成,因此肽构建块有序地组装成超分子结构引起了广泛的兴趣。此外,即使是像二肽这样短的肽,也包含了自发形成纳米和微观尺度有序结构所需的所有分子信息。因此,肽超分子组装已被有效地用于生产具有各种特性的新型材料,这些材料在材料科学、工程、医学和生物学等领域有广泛的应用。为了进一步扩展肽组装在结构和功能复杂性方面的构象空间,多组分(两个或更多)肽超分子共组装最近已经发展成为一种很有前途的扩展方法,类似于天然序列定义生物聚合物(蛋白质)以及合成共价共聚物的结构多样性。这种方法最近在各种应用中得到了证明,例如纳米结构物理尺寸控制、非规范复杂拓扑结构的创建、机械强度调制、光收集软材料的设计、导电器件的制造、诱导荧光、酶催化和组织工程。鉴于近年来肽超分子共组装领域的这些重大进展,在本综述中,我们提供了对这一新兴主题的最新概述和未来展望。