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用于多种肽和蛋白质应用的吖啶基丙氨酸的改进大规模合成

Improved Large-Scale Synthesis of Acridonylalanine for Diverse Peptide and Protein Applications.

作者信息

Marmorstein Jason G, Pagar Vinayak V, Hummingbird Eshe, Saleh Ibrahim G, Phan Hoang Anh T, Chang Yanan, Shaffer Kyle D, Venkatesh Yarra, Dmochowski Ivan J, Stebe Kathleen J, Petersson E James

机构信息

Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104, United States.

Department of Chemical and Biomolecular Engineering, University of Pennsylvania, 220 South 33rd Street, Philadelphia, Pennsylvania 19104, United States.

出版信息

Bioconjug Chem. 2024 Dec 18;35(12):1913-1922. doi: 10.1021/acs.bioconjchem.4c00411. Epub 2024 Nov 12.

Abstract

Fluorescent unnatural amino acids give biochemists, biophysicists, and bioengineers new ways to probe the properties of proteins and peptides. Here, the synthesis of acridon-2-ylalanine (Acd) is optimized for large-scale production to enable ribosomal incorporation through genetic code expansion (GCE), and fluorenylmethoxycarbonyl (Fmoc)-protected Acd is prepared for solid-phase peptide synthesis (SPPS). We demonstrate the utility of Acd in several applications: first, Acd quenching by Tyr is used in the design of fluorescent protease sensors made by SPPS. Second, we demonstrate Acd incorporation into a lanthanide-binding peptide that is generated either by GCE or by SPPS and demonstrate the utility of Acd for sensitizing the emission of Eu. Finally, Acd is inserted into the intrinsically disordered protein, α-synuclein, using GCE and used to study ion binding and aggregation.

摘要

荧光非天然氨基酸为生物化学家、生物物理学家和生物工程师提供了探究蛋白质和肽性质的新方法。在此,吖啶-2-基丙氨酸(Acd)的合成针对大规模生产进行了优化,以通过遗传密码扩展(GCE)实现核糖体掺入,并制备了用于固相肽合成(SPPS)的芴甲氧羰基(Fmoc)保护的Acd。我们展示了Acd在多种应用中的效用:首先,通过SPPS制备的荧光蛋白酶传感器设计中利用了酪氨酸对Acd的淬灭作用。其次,我们证明了Acd可掺入通过GCE或SPPS生成的镧系元素结合肽中,并展示了Acd对增强铕发射的效用。最后,利用GCE将Acd插入内在无序蛋白α-突触核蛋白中,用于研究离子结合和聚集。

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