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蛋白质结构与稳定性的位点特异性研究

Site-Specific Interrogation of Protein Structure and Stability.

机构信息

Department of Chemistry, University of Pennsylvania, Philadelphia, PA, USA.

Department of Biochemistry and Molecular Biophysics, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Methods Mol Biol. 2022;2376:65-87. doi: 10.1007/978-1-0716-1716-8_3.

Abstract

To execute their function or activity, proteins need to possess variability in local electrostatic environment, solvent accessibility, structure, and stability. However, assessing any protein property in a site-specific manner is not easy since native spectroscopic signals often lack the needed specificity. One strategy that overcomes this limitation is to use unnatural amino acids that exhibit distinct spectroscopic features. In this chapter, we describe several such unnatural amino acids (UAAs) and their respective applications in site-specific interrogation of protein structure and stability using standard biophysical methods, including circular dichroism (CD), infrared (IR), and fluorescence spectroscopies.

摘要

为了执行其功能或活动,蛋白质需要在局部静电环境、溶剂可及性、结构和稳定性方面具有可变性。然而,由于天然光谱信号通常缺乏所需的特异性,因此以特定于位置的方式评估任何蛋白质特性并不容易。克服这一限制的一种策略是使用具有独特光谱特征的非天然氨基酸。在本章中,我们描述了几种这样的非天然氨基酸 (UAA) 及其在使用标准生物物理方法(包括圆二色性 (CD)、红外 (IR) 和荧光光谱法)进行蛋白质结构和稳定性的特定位置检测中的各自应用。

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