| Literature DB >> 31147933 |
Abstract
In the endoplasmic reticulum (ER), MHC class I molecules associate with several specialized proteins, forming a large macromolecular complex referred to as the "peptide-loading complex" (PLC). In the PLC, antigenic peptides undergo a stringent selection process that determines which antigen becomes part of the repertoire presented by MHC class I molecules. This ensures that the immune system elicits robust CD8+ T-cell responses to viruses and solid tumors. The ability to reconstitute in vitro MHC class I molecules in association with key proteins of the PLC provides a mean for studying at the molecular level how antigenic peptides are selected for presentation to CD8+ T-cells. Here, we describe practical procedures for generating a cell-free system made up of MHC class I molecules and tapasin that can be used for mechanistic studies of peptide loading and exchange.Entities:
Keywords: Fluorescence anisotropy; MHC class I molecule; Peptide association; Peptide dissociation; Peptide exchange; Peptide-loading complex; Tapasin
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Year: 2019 PMID: 31147933 PMCID: PMC7278038 DOI: 10.1007/978-1-4939-9450-2_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745