Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions

被引:5
作者
Thurairajah, Bethany
Hudson, Andrew J.
Doveston, Richard G. [1 ]
机构
[1] Univ Leicester, Leicester Inst Struct & Chem Biol, Leicester, England
基金
英国工程与自然科学研究理事会;
关键词
14-3-3; fluorescence polarisation; FRET-fluorescence resonance energy transfer; isothermal titration calorimetery; surface plasmon resonace; molecular glues; SMALL-MOLECULE STABILIZATION; BINDING;
D O I
10.3389/fmolb.2022.1043673
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
14-3-3 proteins are a family of regulatory hubs that function through a vast network of protein-protein interactions. Their dysfunction or dysregulation is implicated in a wide range of diseases, and thus they are attractive drug targets, especially for molecular glues that promote protein-protein interactions for therapeutic intervention. However, an incomplete understanding of the molecular mechanisms that underpin 14-3-3 function hampers progress in drug design and development. Biophysical methodologies are an essential element of the 14-3-3 analytical toolbox, but in many cases have not been fully exploited. Here, we present a contemporary review of the predominant biophysical techniques used to study 14-3-3 protein-protein interactions, with a focus on examples that address key questions and challenges in the 14-3-3 field.
引用
收藏
页数:12
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