HIV-1 gp41 and TCRα Trans-Membrane Domains Share a Motif Exploited by the HIV Virus to Modulate T-Cell Proliferation

被引:27
作者
Cohen, Tomer [1 ]
Cohen, Shmuel Jaffe [2 ]
Antonovsky, Niv [1 ]
Cohen, Irun R. [2 ]
Shai, Yechiel [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
基金
以色列科学基金会;
关键词
TYPE-1 ENVELOPE GLYCOPROTEIN; AMINO-ACID-SEQUENCE; PROTEIN-KINASE-C; SYNTHETIC PEPTIDE; ANTIGEN RECEPTOR; IMMUNOLOGICAL SYNAPSE; TRANSMEMBRANE DOMAIN; SPANNING DOMAIN; FUSION PEPTIDE; ACTIVATION;
D O I
10.1371/journal.ppat.1001085
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viruses have evolved several strategies to modify cellular processes and evade the immune response in order to successfully infect, replicate, and persist in the host. By utilizing in-silico testing of a transmembrane sequence library derived from virus protein sequences, we have pin-pointed a nine amino-acid motif shared by a group of different viruses; this motif resembles the transmembrane domain of the alpha-subunit of the T-cell receptor (TCR alpha). The most striking similarity was found within the immunodeficiency virus (SIV and HIV) glycoprotein 41 TMD (gp41 TMD). Previous studies have shown that stable interactions between TCR alpha and CD3 are localized to this nine amino acid motif within TCR alpha, and a peptide derived from it (TCRa TMD, GLRILLLKV) interfered and intervened in the TCR function when added exogenously. We now report that the gp41 TMD peptide co-localizes with CD3 within the TCR complex and inhibits T cell proliferation in vitro. However, the inhibitory mechanism of gp41 TMD differs from that of the TCR alpha TMD and also from the other two known immunosuppressive regions within gp41.
引用
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页数:10
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