Chersi A, Romano T F, Ruocco E
Regina Elena Institute for Cancer Research, Rome, Italy.
Z Naturforsch C J Biosci. 1989 Sep-Oct;44(9-10):886-9. doi: 10.1515/znc-1989-9-1032.
This study indicates that antibodies raised against a DR4,w6; DQw1,3 positive cell line may bind to synthetic peptides selected from the polymorphic amino acid sequences 51-59 and 63-79 on the DQw2 beta chain. This cross-reaction may be explained by the relatively high sequence homology of these sequences in the beta chains of class II histocompatibility antigens, and suggests that antibody binding to small peptides may be scarsely selective. Based on the observations of the reactivity of the antibodies with several cell lines, and comparison of the amino acid sequences of beta chains of DR and DQ molecules, an attempt to identify the cross-reacting epitope is presented.
本研究表明,针对DR4,w6; DQw1,3阳性细胞系产生的抗体可能与从DQw2β链上的多态性氨基酸序列51 - 59和63 - 79中选择的合成肽结合。这种交叉反应可能是由于这些序列在II类组织相容性抗原β链中的相对较高的序列同源性所致,这表明抗体与小肽的结合可能几乎没有选择性。基于对抗体与几种细胞系反应性的观察,以及对DR和DQ分子β链氨基酸序列的比较,本文尝试鉴定交叉反应表位。