Review on the o-Aminoaniline Moiety in Peptide and Protein Chemistry

IF 2.8 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY ChemBioChem Pub Date : 2025-01-23 DOI:10.1002/cbic.202401011
Ziyong Z. Hong
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Abstract

Peptides and proteins are important functional biomolecules both inside and outside of living organisms. The ability to prepare various types of functionalized peptides and proteins is essential for understanding fundamental biological processes, such as protein folding and post-translational modifications (PTMs), and for developing new therapeutics for many diseases, such as cancers and neurodegenerative diseases. The o-aminoaniline moiety was first proposed for activation to a thioester precursor and used for native chemical ligation to prepare large peptides and proteins. In the past decade, the function of o-aminoaniline has been greatly expanded to facilitate the preparation of homogeneously modified peptide and protein samples, where the modifications can include cyclization, C-terminus diversification, etc. Many o-aminoaniline derivatives have also been developed to overcome the inherent limitations of previous versions. In this review, we attempt to summarize the recent developments of different o-aminoaniline derivatives, focusing on their application to the preparation of functional peptide and protein molecules.

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肽和蛋白质化学中邻氨基苯胺部分的研究进展。
多肽和蛋白质是生物体内和体外重要的功能性生物分子。制备各种功能化多肽和蛋白质的能力对于理解蛋白质折叠和翻译后修饰(PTMs)等基本生物学过程以及开发许多疾病(如癌症和神经退行性疾病)的新疗法至关重要。邻氨基苯胺部分首先被提出活化为硫酯前体,并用于天然化学连接以制备大肽和蛋白质。在过去的十年中,邻氨基苯胺的功能得到了极大的扩展,以方便制备均质修饰的肽和蛋白质样品,其中修饰可以包括环化,c端多样化等。许多邻氨基苯胺衍生物也被开发出来,以克服以前版本的固有局限性。本文综述了邻氨基苯胺衍生物的研究进展,重点介绍了邻氨基苯胺衍生物在功能肽和蛋白质分子制备中的应用。
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来源期刊
ChemBioChem
ChemBioChem 生物-生化与分子生物学
CiteScore
6.10
自引率
3.10%
发文量
407
审稿时长
1 months
期刊介绍: ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).
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