Schodin B A, Tsomides T J, Kranz D M
Department of Biochemistry, University of Illinois, Urbana 61801, USA.
Immunity. 1996 Aug;5(2):137-46. doi: 10.1016/s1074-7613(00)80490-2.
The number of T cell receptors on CTL clone 2C that are required for recognition of various peptide-MHC or superantigen-MHC ligands were measured as a function of both the ligand density on target cells and the binding affinity of the TCR. Quantitative inverse correlations were determined between the number of TCRs required for recognition and the number of ligands on target cells, and the number of TCR required and the Ka of the TCR for the ligand. We propose and test predictive uses of these relationships to determine the number of endogenous peptide-MHC complexes on a target cell (when TCR affinity is known) or to determine the affinity of the TCR (when the number of ligands is known).
测量了CTL克隆2C上识别各种肽-MHC或超抗原-MHC配体所需的T细胞受体数量,该数量是靶细胞上配体密度和TCR结合亲和力的函数。确定了识别所需的TCR数量与靶细胞上配体数量之间以及所需的TCR数量与TCR对配体的解离常数(Ka)之间的定量负相关关系。我们提出并测试了这些关系的预测用途,以确定靶细胞上内源性肽-MHC复合物的数量(当TCR亲和力已知时)或确定TCR的亲和力(当配体数量已知时)。