Decoupling peptide binding from T cell receptor recognition with engineered chimeric MHC-I molecules

نویسندگان

چکیده

Abstract Human leucocyte antigens (HLAs) display a repertoire of epitopic peptides on the cell surface for T recognition. Amino acid polymorphisms in peptide-binding groove different HLA allotypes result distinct antigenic repertoires, providing basis adaptive immunity to emerging pathogens at population level. receptors (TCRs) recognize pHLA through interactions with both peptide and heavy chain residues. In this work, we use structural data from peptide:MHC-I pMHC:TCR structures identify residues important and/or TCR binding, outline fixed-backbone computational design approach engineering synthetic molecules that combine binding recognition surfaces existing allotypes. X-ray crystallography demonstrates chimeric bridging divergent alleles can bind selected specified backbone conformation. Moreover, vitro tetramer staining biophysical experiments using pMHC-I presenting established further demonstrate requirement framework residues, as opposed peptide-centric Chimeric Antigen Receptors (CARs). Our results underscore novel, structure-guided platform developing displaying tumor-associated modified interaction surfaces, which could serve platforms elicit alloreactive responses against self-antigens are overexpressed cancer. Finally, gain deeper understanding evolution functional divergence by demonstrating an example convergent evolution. Supported grants NIAID (5R01AI143997), NIGMS (5R35GM125034), NIDDK (5U01DK112217)

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ژورنال

عنوان ژورنال: Journal of Immunology

سال: 2023

ISSN: ['1550-6606', '0022-1767']

DOI: https://doi.org/10.4049/jimmunol.210.supp.251.06