Schwartz M, Waltenbaugh C, Dorf M, Cesla R, Sela M, Benacerraf B
Proc Natl Acad Sci U S A. 1976 Aug;73(8):2862-6. doi: 10.1073/pnas.73.8.2862.
The ability of mice bearing the H-2S haplotype to develop helper responses to the random copolymer of Glu,Ala while they developed suppressor responses to the terpolymer of Glu,Ala,Tyr suggested the crucial role of tyrosine in these peptides. On the basis of various considerations, it was postulated that many of the tyrosine residues in Glu,Ala,Tyr would be localized at the NH2-terminal end of the molecule. To verify this hypothesis, a block terpolymer composed of a short sequence of homopolymer tyrosine covalently bound to the random copolymer of Glu,Ala was synthesized. The present studies, using this block terpolymer, demonstrated that the chemical determinants stimulating helper and suppressor responses are distinct and can be present simultaneously in the same molecule. Thus, addition of COOH-terminal tyrosine residues to the Glu,Ala polypeptide converted this immunogenic molecule to an immunosuppressive molecule in mice bearing the H-2S haplotype. The mechanism by which these short sequences of tyrosine influence H-2-linked immune responses remains to be determined.
携带H-2S单倍型的小鼠能够对Glu、Ala的无规共聚物产生辅助性反应,而对Glu、Ala、Tyr的三元共聚物产生抑制性反应,这表明酪氨酸在这些肽中起着关键作用。基于各种考虑,推测Glu、Ala、Tyr中的许多酪氨酸残基会位于分子的NH2末端。为了验证这一假设,合成了一种由短序列的均聚酪氨酸共价连接到Glu、Ala的无规共聚物上的嵌段三元共聚物。本研究使用这种嵌段三元共聚物证明,刺激辅助性和抑制性反应的化学决定簇是不同的,并且可以同时存在于同一分子中。因此,在Glu、Ala多肽上添加COOH末端的酪氨酸残基,可将这种免疫原性分子转化为携带H-2S单倍型小鼠体内的免疫抑制分子。这些短序列酪氨酸影响H-2连锁免疫反应的机制仍有待确定。