Enhancing and inhibitory motifs regulate CD4 activity

被引:2
作者
Lee, Mark S. [1 ]
Tuohy, Peter J. [1 ]
Kim, Caleb Y. [1 ]
Lichauco, Katrina [1 ]
Parrish, Heather L. [1 ]
Van Doorslaer, Koenraad [1 ,2 ,3 ,4 ,5 ]
Kuhns, Michael S. [1 ,3 ,4 ,5 ,6 ]
McLaughlin, Richard N.
机构
[1] Univ Arizona, Coll Med, Dept Immunobiol, Tucson, AZ 85721 USA
[2] Univ Arizona, Sch Anim & Comparat Biomed Sci, Tucson, AZ 85721 USA
[3] Univ Arizona, Canc Biol Grad Interdisciplinary Program, Tucson, AZ 85721 USA
[4] Univ Arizona, Genet Grad Interdisciplinary Program, Tucson, AZ 85721 USA
[5] Univ Arizona, Inst Bio5, Tucson, AZ 85721 USA
[6] Univ Arizona, Arizona Ctr Aging, Coll Med, Tucson, AZ 85721 USA
来源
ELIFE | 2022年 / 11卷
关键词
T cell; CD4; evolution; TCR; signaling; activation; EVOLUTIONARY CONSERVATION; JUXTAMEMBRANE REGIONS; SEQUENCE ALIGNMENT; PROTEINS; LCK; PALMITOYLATION; IDENTIFICATION; ASSOCIATION; SITES; ORGANIZATION;
D O I
10.7554/eLife.79508
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
CD4(+) T cells use T cell receptor (TCR)-CD3 complexes, and CD4, to respond to peptide antigens within MHCII molecules (pMHCII). We report here that, through similar to 435 million years of evolution in jawed vertebrates, purifying selection has shaped motifs in the extracellular, transmembrane, and intracellular domains of eutherian CD4 that enhance pMHCII responses, and covary with residues in an intracellular motif that inhibits responses. Importantly, while CD4 interactions with the Src kinase, Lck, are viewed as key to pMHCII responses, our data indicate that CD4-Lck interactions derive their importance from the counterbalancing activity of the inhibitory motif, as well as motifs that direct CD4-Lck pairs to specific membrane compartments. These results have implications for the evolution and function of complex transmembrane receptors and for biomimetic engineering.
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页数:29
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