Jemmerson R, Morrow P R, Klinman N R, Paterson Y
Proc Natl Acad Sci U S A. 1985 Mar;82(5):1508-12. doi: 10.1073/pnas.82.5.1508.
Two synthetic peptides inclusive of the NH2-terminal N-acetyl-Gly-Asp-Val-Glu tetrapeptide of mammalian cytochrome c (cyt c) were used in this study to address the question of whether mammals can respond immunologically to an evolutionarily conserved region of a protein. These peptides were assessed for their capacity (i) to act as immunogens for the production of anti-self cyt c antisera and (ii) to bind rabbit anti-rodent cyt c antibody. The findings from these studies indicate the existence of an immunogenic determinant in an evolutionarily conserved region of cyt c that contains residues 1-4. This determinant can induce anti-self cyt c antibodies whether presented as a peptide on a carrier protein or in the context of the intact molecule as polymerized mammalian cyt c.
本研究使用了两种包含哺乳动物细胞色素c(cyt c)NH2末端N - 乙酰 - 甘氨酸 - 天冬氨酸 - 缬氨酸 - 谷氨酸四肽的合成肽,以探讨哺乳动物是否能对蛋白质的进化保守区域产生免疫反应这一问题。对这些肽进行了评估,以确定它们(i)作为免疫原产生抗自身cyt c抗血清的能力,以及(ii)与兔抗啮齿动物cyt c抗体结合的能力。这些研究结果表明,在cyt c的进化保守区域中存在一个免疫原性决定簇,该区域包含第1 - 4位残基。无论该决定簇是以肽的形式呈现在载体蛋白上,还是以聚合的哺乳动物cyt c完整分子的形式呈现,都能诱导产生抗自身cyt c抗体。