MHC Class II Tetramers Made from Isolated Recombinant α and β Chains Refolded with Affinity-Tagged Peptides

被引:12
作者
Braendstrup, Peter [1 ,2 ]
Justesen, Sune [1 ]
Osterbye, Thomas [1 ]
Nielsen, Lise Lotte Bruun [1 ]
Mallone, Roberto [3 ]
Vindelov, Lars [2 ]
Stryhn, Anette [1 ]
Buus, Soren [1 ]
机构
[1] Univ Copenhagen, Expt Immunol Lab, Copenhagen, Denmark
[2] Rigshosp, Dept Hematol, Allogene Hematopoiet Cell Transplantat Lab, DK-2100 Copenhagen, Denmark
[3] INSERM, Cochin Inst, U1016, DeAR Lab Avenir, Paris, France
关键词
CD4(+) T-CELLS; HEPATITIS-C VIRUS; REPERTOIRE SELECTION; ANTIGEN; MOLECULES; COMPLEX; EPITOPE; ACTIVATION; INFECTION; STRATEGY;
D O I
10.1371/journal.pone.0073648
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Targeting CD4+ T cells through their unique antigen-specific, MHC class II-restricted T cell receptor makes MHC class II tetramers an attractive strategy to identify, validate and manipulate these cells at the single cell level. Currently, generating class II tetramers is a specialized undertaking effectively limiting their use and emphasizing the need for improved methods of production. Using class II chains expressed individually in E. coli as versatile recombinant reagents, we have previously generated peptide-MHC class II monomers, but failed to generate functional class II tetramers. Adding a monomer purification principle based upon affinity-tagged peptides, we here provide a robust method to produce class II tetramers and demonstrate staining of antigen-specific CD4+ T cells. We also provide evidence that both MHC class II and T cell receptor molecules largely accept affinity-tagged peptides. As a general approach to class II tetramer generation, this method should support rational CD4+ T cell epitope discovery as well as enable specific monitoring and manipulation of CD4+ T cell responses.
引用
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页数:12
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