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Peptide‐Scaffolded Detergents for Membrane Protein Studies.

  • Published In: Chemistry - A European Journal, 2025, v. 31, n. 16. P. 1 1 of 3

  • Database: Academic Search Ultimate 2 of 3

  • Authored By: Yang, Meifang; Dai, Yili; Zhou, Fang; Zhou, Xin; Qiu, Yanli; Tan, Yan; Zhao, Suwen; Xue, Dongxiang; Zhao, Fei; Tao, Houchao 3 of 3

Abstract

Detergents are essential for preserving the structural integrity and functionality of membrane proteins (MPs) outside the biological membrane or in aqueous solution, and thus ensuring accurate biochemical and structural analyses. Here, we introduce peptide‐scaffolded detergents, a novel class of hybrid molecules formed by preassembling detergent monomers with peptides of varying lengths, mediated via Click chemistry. These detergents are characterized by scalable, straightforward synthesis and enhanced solubility. Among the variants, A4B2 emerged as the optimal detergent, demonstrating superior thermal stabilization across a range of G protein‐coupled receptors, including A2AAR, SMO and GLP‐1R. Additionally, A4B2 exhibits a low critical micelle concentration and small micelle size, together making it particularly effective for electron microscopy studies of A2AAR. This innovative design leverages the benefits of peptide‐based and traditional detergents, offering new insights for the development of advanced detergents in MP research. [ABSTRACT FROM AUTHOR]

Additional Information

  • Source:Chemistry - A European Journal. 2025/03, Vol. 31, Issue 16, p1
  • Document Type:Article
  • Subject Area:Science
  • Publication Date:2025
  • ISSN:0947-6539
  • DOI:10.1002/chem.202404520
  • Accession Number:183823123
  • Copyright Statement:Copyright of Chemistry - A European Journal is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

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