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
相关论文
共 50 条
  • [1] Analysing the role of the CTLA-4 cytoplasmic domain in intracellular trafficking
    Kaur, S.
    Qureshi, O.
    Sansom, D. M.
    IMMUNOLOGY, 2010, 131 : 90 - 90
  • [2] CTLA-4 lacking the cytoplasmic domain costimulates IL-2 production
    Matzkies, F
    Manger, B
    Kalden, JR
    Nagel, T
    FASEB JOURNAL, 1999, 13 (04): : A628 - A628
  • [3] A regulatory role for cytoplasmic YVKM motif in CTLA-4 inhibition of TCR signaling
    Schneider, H
    Dias, SD
    Hu, H
    Rudd, CE
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2001, 31 (07) : 2042 - 2050
  • [4] The role of cytoplasmic YVKM motif in CTLA-4 inhibition of TCR signaling.
    Dias, SD
    Schneider, H
    Hu, H
    Rudd, CE
    BLOOD, 2001, 98 (11) : 509A - 509A
  • [5] CTLA-4 lacking the cytoplasmic domain costimulates IL-2 production.
    Nagel, T
    Matzkies, F
    Kalden, JR
    Manger, B
    ARTHRITIS AND RHEUMATISM, 1999, 42 (09): : S262 - S262
  • [6] The cytoplasmic domain of CTLA-4 control autoimmunity via inducing regulatory T cells
    Kim, Gil-Ran
    Lim, Sangho
    Lee, Jae-Ung
    Choi, Je-Min
    JOURNAL OF IMMUNOLOGY, 2019, 202 (01):
  • [7] CTLA-4 gene polymorphisms and natural soluble CTLA-4 protein in psoriasis vulgaris
    Luszczek, W.
    Kubicka, W.
    Jasek, M.
    Baran, E.
    Cislo, M.
    Nockowski, P.
    Luczywo-Rudy, M.
    Wisniewski, A.
    Nowak, I.
    Kusnierczyk, P.
    INTERNATIONAL JOURNAL OF IMMUNOGENETICS, 2006, 33 (03) : 217 - 224
  • [8] HUMAN IG SUPERFAMILY CTLA-4 GENE - CHROMOSOMAL LOCALIZATION AND IDENTITY OF PROTEIN-SEQUENCE BETWEEN MURINE AND HUMAN CTLA-4 CYTOPLASMIC DOMAINS
    DARIAVACH, P
    MATTEI, MG
    GOLSTEIN, P
    LEFRANC, MP
    EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (12) : 1901 - 1905
  • [9] CTLA-4 gene mutation and multiple sclerosis: A case report and literature review
    Lin, Ting-Wei
    Hu, Ya-Chiao
    Yang, Yao-Hsu
    Chien, Yin-Hsiu
    Lee, Ni-Chung
    Yu, Hsin-Hui
    Chiang, Bor-Luen
    Wang, Li-Chieh
    JOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION, 2022, 55 (03) : 545 - 548
  • [10] Intranasal delivery of the cytoplasmic domain of CTLA-4 using a novel protein transduction domain prevents allergic inflammation
    Je-Min Choi
    Mi-Hyun Ahn
    Wook-Jin Chae
    Yung-Gook Jung
    Jae-Chul Park
    Hyun-Mi Song
    Young-Eun Kim
    Jung-Ah Shin
    Choon-Sik Park
    Jung-Won Park
    Tae-Kwann Park
    Jung-Hoon Lee
    Byung-Fhy Seo
    Kyun-Do Kim
    Eun-Sung Kim
    Dong-Ho Lee
    Seung-Kyou Lee
    Sang-Kyou Lee
    Nature Medicine, 2006, 12 : 574 - 579