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[乙型肝炎病毒核心蛋白中央部分的异源表位]

[Heterologous epitopes in the central part of the hepatitis B virus core protein].

作者信息

Makeeva I V, Kalinina T I, Khudiakov Iu E, Samoshin V V, Smirnova E A, Semiletov Iu A, Pavliuchenkova R P, Kadoshnikov Iu P, Smirnov V D

出版信息

Mol Biol (Mosk). 1995 Jan-Feb;29(1):211-24.

PMID:7723761
Abstract

A set of plasmids was constructed determining synthesis of hybrid proteins with insertions of antigenic determinants of preS1 and preS2 regions of HBV in the middle part of HBcAg. The polypeptides containing the 31-36 or monomeric 94-105 preS1 epitopes were water-soluble and formed particles similar to the 27-nm ones of native HBcAg, possessing antigenic properties of both HBcAg and the inserted epitope, while the hybrids containing 133-143 of preS2 or a trimeric form of the 94-105 preS1 epitope became membrane-bound. Another hybrid encoded by plasmid pPS2M31 contained two regions of HBcAg modification: insertion of amino acids 133-143 a.a. (preS2 region) in the N-terminal part and 31-36 (preS1) in the middle part of the carrier. The immunogenicity of the epitope inserted into the middle part of the HBcAg molecule was an order of magnitude higher than that of the same epitope in the N-part of the protein; the fact might be important for constructing artificial immunogens.

摘要

构建了一组质粒,用于确定在HBcAg中部插入HBV preS1和preS2区域抗原决定簇的杂合蛋白的合成。含有31 - 36或单体94 - 105 preS1表位的多肽是水溶性的,并形成类似于天然HBcAg 27纳米颗粒的颗粒,具有HBcAg和插入表位的抗原特性,而含有preS2的133 - 143或三聚体形式的94 - 105 preS1表位的杂合体则与膜结合。由质粒pPS2M31编码的另一种杂合体包含两个HBcAg修饰区域:在载体的N端插入133 - 143个氨基酸(preS2区域),在中部插入31 - 36(preS1)。插入到HBcAg分子中部的表位的免疫原性比在蛋白质N端的相同表位高一个数量级;这一事实对于构建人工免疫原可能很重要。

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