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Production and Thermal Exchange of Conditional Peptide‐MHC I Multimers

Cytotoxic CD8(+) T cells mediate cellular immunity through recognition of specific antigens presented by MHC class I on all nucleated cells. Studying T cell interactions and responses provides invaluable information on infection, autoimmunity and cancer. Fluorescently labeled multimers of MHC I can...

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Detalles Bibliográficos
Autores principales: Luimstra, Jolien J., Franken, Kees L. M. C., Garstka, Malgorzata A., Drijfhout, Jan W., Neefjes, Jacques, Ovaa, Huib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852010/
https://www.ncbi.nlm.nih.gov/pubmed/31483102
http://dx.doi.org/10.1002/cpim.85
Descripción
Sumario:Cytotoxic CD8(+) T cells mediate cellular immunity through recognition of specific antigens presented by MHC class I on all nucleated cells. Studying T cell interactions and responses provides invaluable information on infection, autoimmunity and cancer. Fluorescently labeled multimers of MHC I can be used to quantify, characterize, and isolate specific CD8(+) T cells by flow cytometry. Here we describe the production and use of conditional MHC I multimers that can be loaded with peptides of choice by incubating them at a defined temperature. Multimers are folded with a template peptide that forms a stable complex at low temperature, but dissociates at a defined elevated temperature. Using this technology multiple MHC I multimers can be generated in parallel, to allow staining and isolation of large sets of antigen‐specific CD8(+) T cells, especially when combined with barcoding technologies. © 2019 The Authors.