Peptide Tectonics: Encoded Structural Complementarity Dictates Programmable Self-Assembly.

biomaterials conformational entropy hierarchical nanostructures peptides self‐assembly supramolecular chemistry

Journal

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
ISSN: 2198-3844
Titre abrégé: Adv Sci (Weinh)
Pays: Germany
ID NLM: 101664569

Informations de publication

Date de publication:
03 Jul 2019
Historique:
received: 12 11 2018
revised: 20 03 2019
entrez: 6 8 2019
pubmed: 6 8 2019
medline: 6 8 2019
Statut: epublish

Résumé

Programmable self-assembly of peptides into well-defined nanostructures represents one promising approach for bioinspired and biomimetic synthesis of artificial complex systems and functional materials. Despite the progress made over the past two decades in the development of strategies for precise manipulation of the self-assembly of peptides, there is a remarkable gap between current peptide assemblies and biological systems in terms of structural complexity and functions. Here, the concept of peptide tectonics for the creation of well-defined nanostructures predominately driven by the complementary association at the interacting interfaces of tectons is introduced. Peptide tectons are defined as peptide building blocks exhibiting structural complementarity at the interacting interfaces of commensurate domains and undergoing programmable self-assembly into defined supramolecular structures promoted by complementary interactions. Peptide tectons are categorized based on their conformational entropy and the underlying mechanism for the programmable self-assembly of peptide tectons is highlighted focusing on the approaches for incorporating the structural complementarity within tectons. Peptide tectonics not only provides an alternative perspective to understand the self-assembly of peptides, but also allows for precise manipulation of peptide interactions, thus leading to artificial systems with advanced complexity and functions and paves the way toward peptide-related functional materials resembling natural systems.

Identifiants

pubmed: 31380179
doi: 10.1002/advs.201802043
pii: ADVS1103
pmc: PMC6662064
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1802043

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Shaofeng Lou (S)

Key Laboratory of Functional Polymer Materials, Ministry of Education State Key Laboratory of Medicinal Chemical Biology Institute of Polymer Chemistry College of Chemistry Nankai University Weijin Road 94 Tianjin 300071 China.

Xinmou Wang (X)

Key Laboratory of Functional Polymer Materials, Ministry of Education State Key Laboratory of Medicinal Chemical Biology Institute of Polymer Chemistry College of Chemistry Nankai University Weijin Road 94 Tianjin 300071 China.

Zhilin Yu (Z)

Key Laboratory of Functional Polymer Materials, Ministry of Education State Key Laboratory of Medicinal Chemical Biology Institute of Polymer Chemistry College of Chemistry Nankai University Weijin Road 94 Tianjin 300071 China.

Linqi Shi (L)

Key Laboratory of Functional Polymer Materials, Ministry of Education State Key Laboratory of Medicinal Chemical Biology Institute of Polymer Chemistry College of Chemistry Nankai University Weijin Road 94 Tianjin 300071 China.

Classifications MeSH