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用多种方法重新研究常见的蛋白质-配体相互作用。

A Familiar Protein-Ligand Interaction Revisited with Multiple Methods.

机构信息

Biophysics Facility, Biozentrum, University of Basel, Basel, Switzerland.

出版信息

Methods Mol Biol. 2021;2263:47-79. doi: 10.1007/978-1-0716-1197-5_2.

Abstract

The interaction of hen egg white lysozyme with the trisaccharide tri-N-acetyl glucosamine has been well-characterized by biophysical methods and structural biology. In this chapter, we present a series of experiments designed to detect and quantify that interaction using several commonly available biophysical methods: thermal shift assay, fluorescence intensity, microscale thermophoresis, isothermal titration calorimetry, and surface plasmon resonance.These experiments have been used for teaching and troubleshooting in a core facility. By taking a set of representative data from several years of practical courses, we are able to demonstrate the robustness of the protocols, calculate confidence intervals for the dissociation constant from each method, and illustrate the degree of consistency between those methods when applied to a simple system in a single location by different experimenters.

摘要

通过生物物理方法和结构生物学,已经很好地描述了蛋清溶菌酶与三糖三-N-乙酰氨基葡萄糖的相互作用。在本章中,我们设计了一系列实验,使用几种常用的生物物理方法来检测和定量这种相互作用:热位移分析、荧光强度、微量热泳动、等温滴定量热法和表面等离子体共振。这些实验已在核心设施中用于教学和故障排除。通过从几年的实践课程中获取一组有代表性的数据,我们能够证明方案的稳健性,从每种方法计算出离解常数的置信区间,并说明当由不同的实验者在单个位置应用于简单系统时,这些方法之间的一致性程度。

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