Issue 23, 2024

Molecular recognition of peptides and proteins by cucurbit[n]urils: systems and applications

Abstract

The development of methodology for attaching ligand binding sites to proteins of interest has accelerated biomedical science. Such protein tags have widespread applications as well as properties that significantly limit their utility. This review describes the mechanisms and applications of supramolecular systems comprising the synthetic receptors cucurbit[7]uril (Q7) or cucurbit[8]uril (Q8) and their polypeptide ligands. Molecular recognition of peptides and proteins occurs at sites of 1–3 amino acids with high selectivity and affinity via several distinct mechanisms, which are supported by extensive thermodynamic and structural studies in aqueous media. The commercial availability, low cost, high stability, and biocompatibility of these synthetic receptors has led to the development of myriad applications. This comprehensive review compiles the molecular recognition studies and the resulting applications with the goals of providing a valuable resource to the community and inspiring the next generation of innovation.

Graphical abstract: Molecular recognition of peptides and proteins by cucurbit[n]urils: systems and applications

Article information

Article type
Review Article
Submitted
07 Jun 2024
First published
17 Oct 2024
This article is Open Access
Creative Commons BY-NC license

Chem. Soc. Rev., 2024,53, 11519-11556

Molecular recognition of peptides and proteins by cucurbit[n]urils: systems and applications

L. Armstrong, S. L. Chang, N. Clements, Z. Hirani, L. B. Kimberly, K. Odoi-Adams, P. Suating, H. F. Taylor, S. A. Trauth and A. R. Urbach, Chem. Soc. Rev., 2024, 53, 11519 DOI: 10.1039/D4CS00569D

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements