Burrows S R, Suhrbier A, Khanna R, Moss D J
Queensland Institute of Medical Research, Bancroft Centre, Brisbane, Australia.
Immunology. 1992 May;76(1):174-5.
Synthetic peptides are widely used to define the specificity of CD8+ cytotoxic T-lymphocyte (CTL) clones. When many peptides need to be tested by the standard chromium release assay large numbers of a CTL clone are required. Specific synthetic peptide epitopes induce CTL clones to kill each other. This phenomenon can be directly visualized using an inverted microscope and forms the basis for a convenient assay, which can be performed with as few as 100 CTL per peptide and does not require radiolabelled targets.
合成肽被广泛用于确定CD8 + 细胞毒性T淋巴细胞(CTL)克隆的特异性。当需要通过标准的铬释放试验检测多种肽时,就需要大量的CTL克隆。特定的合成肽表位可诱导CTL克隆相互杀伤。使用倒置显微镜可直接观察到这种现象,这构成了一种便捷检测方法的基础,该方法每种肽仅需100个CTL即可进行,且不需要放射性标记的靶细胞。