发布: 2017年07月05日第7卷第13期 DOI: 10.21769/BioProtoc.2366 浏览次数: 8693
评审: Jia LiAna Santos AlmeidaPalash Kanti DuttaAnonymous reviewer(s)
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Hironori Saito [...] Shintaro Iwasaki
2023年02月05日 1146 阅读
Abstract
T cell receptor (TCR) recognition of foreign peptide fragments, presented by peptide major histocompatibility complex (pMHC), governs T-cell mediated protection against pathogens and cancer. Many factors govern T-cell sensitivity, including the affinity of the TCR-pMHC interaction and the stability of pMHC on the surface of antigen presenting cells. These factors are particularly relevant for the peptide vaccination field, in which more stable pMHC interactions could enable more effective protection against disease. Here, we discuss a method for the determination of pMHC stability that we have used to investigate HIV immune escape, T-cell sensitivity to cancer antigens and mechanisms leading to autoimmunity.
Keywords: Peptide-MHC stability (肽MHC稳定性)Background
The ability of CD8+ T-cells to respond to foreign invaders or dysregulated self is dependent on stable pMHC class I (pMHCI) presentation at the cell surface. Structurally, MHCI molecules form a peptide binding groove formed of two parallel α helices with a floor of β sheets at the interface between the α1 and α2 domains (Latron et al., 1992). The peptide binding groove has primary peptide binding pockets (B and F) that tightly interact with specific amino acids towards the N- and C-terminals of bound peptides. Although these pockets can accommodate a range of amino acids, they exhibit preferences for certain side chains that have been characterized using structural and biochemical approaches (Parker et al., 1992). This information has been used to generate so called ‘heteroclitic’ peptides in which natural peptides that have poor MHC-anchors can be modified with amino acids that bind optimally to MHC for vaccination (Cole et al., 2010). Moreover, pMHC stability has been linked to HIV immune escape (Bronke et al., 2013) and the selection of autoreactive T-cell clones (Yin et al., 2011). Thus, understanding the mechanisms that control pMHC stability is important for therapeutic design and understanding complex human diseases. Here, we developed a protocol to accurately determine pMHC stability using circular dichroism spectroscopy. We have used this technique, together with structural, biophysical and cellular experiments, to provide new insight into the molecular factors that determined T-cell antigen recognition in the context of a range of human diseases (Kløverpris et al., 2015; Knight et al., 2015; Motozono et al., 2015; Cole et al., 2016; Jones et al., 2016; Cole et al., 2017).
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版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Fuller, A., Wall, A., Crowther, M. D., Lloyd, A., Zhurov, A., Sewell, A. K., Cole, D. K. and Beck, K. (2017). Thermal Stability of Heterotrimeric pMHC Proteins as Determined by Circular Dichroism Spectroscopy. Bio-protocol 7(13): e2366. DOI: 10.21769/BioProtoc.2366.
分类
免疫学 > 免疫细胞染色 > 免疫检测
细胞生物学 > 细胞染色 > 蛋白质
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