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Immunological and Biophysical Separation of Dengue-2 Antigens

机译:登革热2抗原的免疫和生物物理分离

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Antigenic compositions of slowly sedimenting dengue-2 hemagglutinin (SHA) and soluble complement-fixing antigen (SCF) were compared with the virion (rapidly sedimenting hemagglutinin, RHA) by radioimmune precipitation (RIP), RIP inhibition, kinetic neutralization, and neutralization blocking tests with the use of hyperimmune mouse ascitic fluids. RHA and SHA were unable to inhibit completely the RIP of each other by anti-RHA, and neutralization by anti-RHA was not blocked by SHA. This indicated that SHA is serologically related, but not identical, to RHA. SHA differed from RHA in that SHA lacked the “core” polypeptide but contained the two envelope polypeptides. In addition, SHA contained a polypeptide with a molecular weight of 16,500 daltons and a suggestion of several other proteins. These data, when considered with other evidence, suggest that SHA is a special form of “incomplete virus.” SCF was unable to inhibit the RIP of SHA or RHA or to block neutralizing antibodies. Further, anti-SCF did not neutralize RHA or precipitate significant levels of SHA or RHA. Polyacrylamide gel electrophoresis separated SCF from structural polypeptides by molecular size. This evidence suggests that SCF is a nonstructural antigen.
机译:将慢沉淀的抗原 - 2血凝素(SHA)和可溶性补体固定抗原(SCF)进行抗原组合物与Regimmune沉淀(RIP),RIP抑制,动力学中和和中和阻断测试进行比较(迅速沉淀的血凝素,Rha)。随着超微征鼠标腹水液体的使用。 rha和Sha无法完全抑制抗rha彼此的撕裂,并且抗rha的中和不被沙子阻塞。这表明SHA在旋律相关,但不相同到RHA。 SHA与rha不同,因为Sha缺乏“核心”多肽,但含有两个包络多肽。此外,SHA含有分子量为16,500道尔顿的多肽,以及其他几种蛋白质的建议。这些数据在考虑到其他证据时,建议沙是“不完全病毒”的特殊形式。 SCF无法抑制SHA或RHA的裂口或阻断中和抗体。此外,抗SCF未中和RHA或沉淀显着水平的SHA或RHA。聚丙烯酰胺凝胶电泳通过分子尺寸将SCF与结构多肽分离。该证据表明,SCF是非结构抗原。

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