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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.
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页数:12
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