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[口蹄疫病毒的抗原结构。II. A22型口蹄疫病毒VP1蛋白主要免疫原区保护性肽的合成]

[Antigenic structure of the foot-and-mouth disease virus. II. Synthesis of protective peptides from the major immunogenic region of VP1 protein of foot-and-mouth disease virus type A22].

作者信息

Vol'pina O M, Surovoĭ A Iu, Ul'iashin V V, Ivanov V T, Chepurkin A V

出版信息

Bioorg Khim. 1988 Oct;14(10):1363-71.

PMID:2852938
Abstract

Earlier we found that the immune response and antiviral protection from FMDV can be achieved by immunization with uncoupled FMDV peptides. In a search of approaches to animal protection from FMDV A22 strain we prepared a series of peptides corresponding to the putative antigenic determinants. Synthetic 131-149 and 140-149 sequences afforded 50 to 80% protection, both in the free state and conjugated with keyhole limpet hemocyanin. We believe that the 140-149 segment is so far the smallest peptide capable of eliciting specific antiviral protection without conjugation with a high molecular carrier.

摘要

早些时候我们发现,通过用未偶联的口蹄疫病毒(FMDV)肽进行免疫,可以实现对FMDV的免疫应答和抗病毒保护。在寻找保护动物免受FMDV A22株感染的方法时,我们制备了一系列对应于推定抗原决定簇的肽。合成的131-149和140-149序列,无论是游离状态还是与钥孔血蓝蛋白偶联,都能提供50%至80%的保护。我们认为,140-149片段是迄今为止能够在不与高分子载体偶联的情况下引发特异性抗病毒保护的最小肽。

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