Circular dichroism determination of class I MHC-peptide equilibrium dissociation constants

被引:35
作者
Morgan, CS
Holton, JM
Olafson, BD
Bjorkman, PJ
Mayo, SL
机构
[1] CALTECH,HOWARD HUGHES MED INST,DIV BIOL,PASADENA,CA 91125
[2] CALTECH,DIV CHEM & CHEM ENGN,PASADENA,CA 91125
[3] CALTECH,HOWARD HUGHES MED INST,PASADENA,CA 91125
关键词
circular dichroism; class I MHC; dissociation constant;
D O I
10.1002/pro.5560060819
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Class I major histocompatibility complex (MHC) molecules bind peptides derived from degraded proteins for display to T cells of the immune system. Peptides bind to MHC proteins with varying affinities, depending upon their sequence and length. We demonstrate that the thermal stability of the MHC-peptide complex depends directly on peptide binding affinity. We use this correlation to develop a convenient method to determine peptide dissociation constants by measuring MHC-peptide complex stability using thermal denaturation profiles monitored by circular dichroism.
引用
收藏
页码:1771 / 1773
页数:3
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