Mechanistic Insights into the Inhibition of a Common CTLA-4 Gene Mutation in the Cytoplasmic Domain

被引:2
|
作者
Xu, Jikang [1 ,2 ]
Zhang, Yu [1 ,2 ]
Shen, Lijuan [1 ]
Du, Lingyu [1 ]
Xue, Hongjuan [3 ]
Wu, Bin [3 ]
OuYang, Bo [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biochem & Cell Biol, State Key Lab Mol Biol, Ctr Excellence Mol Cell Sci, Shanghai 200031, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Zhangjiang Lab, Natl Facil Prot Sci Shanghai, Shanghai Adv Res Inst, Shanghai 201203, Peoples R China
来源
MOLECULES | 2024年 / 29卷 / 06期
基金
国家重点研发计划;
关键词
CTLA-4; G199R; NMR spectroscopy; lipid regulation; inhibitory mechanism; T-CELLS; PROTEIN; CD28; ASSOCIATION; RECEPTOR; LOCALIZATION; SUPERFAMILY; EXPRESSION; SEQUENCE; VARIANTS;
D O I
10.3390/molecules29061330
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
Cytotoxic T-lymphocyte antigen 4 (CTLA-4) is a pivotal immune checkpoint receptor, playing a crucial role in modulating T-cell activation. In this study, we delved into the underlying mechanism by which a common mutation, G199R, in the cytoplasmic domain of CTLA-4 impacts its inhibitory function. Utilizing nuclear magnetic resonance (NMR) spectroscopy and biochemical techniques, we mapped the conformational changes induced by this mutation and investigated its role in CTLA-4 activity. Our findings reveal that this mutation leads to a distinct conformational alteration, enhancing protein-membrane interactions. Moreover, functional assays demonstrated an improved capacity of the G199R mutant to downregulate T-cell activation, underscoring its potential role in immune-related disorders. These results not only enhance our understanding of CTLA-4 regulatory mechanisms but also provide insights for targeted therapeutic strategies addressing immune dysregulation linked to CTLA-4 mutations.
引用
收藏
页数:15
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