Affiliation
Department of Immunobiology, University of Arizona College of MedicineSchool of Animal and Comparative Biomedical Sciences, University of Arizona
Cancer Biology Graduate Interdisciplinary Program and Genetics Graduate Interdisciplinary Program, University of Arizona
BIO-5 Institute, University of Arizona
University of Arizona Cancer Center
Cancer Biology Graduate Interdisciplinary Program, University of Arizona
Genetics Graduate Interdisciplinary Program, University of Arizona
Arizona Center on Aging, University of Arizona College of Medicine
Issue Date
2022
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ELIFE SCIENCES PUBLICATIONS LTDCitation
Lee, M. S., Tuohy, P. J., Kim, C. Y., Lichauco, K., Parrish, H. L., Van Doorslaer, K., & Kuhns, M. S. (2022). Enhancing and inhibitory motifs regulate CD4 activity. ELife, 11.Journal
eLifeRights
Copyright © Lee et al. This article is distributed under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
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 ~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. © 2022, Lee et al.Note
Open access journalISSN
2050-084XPubMed ID
35861317Version
Final published versionae974a485f413a2113503eed53cd6c53
10.7554/eLife.79508
Scopus Count
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Except where otherwise noted, this item's license is described as Copyright © Lee et al. This article is distributed under the terms of the Creative Commons Attribution License.
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