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在受感染细胞内发现的多重电荷莫洛尼鼠白血病病毒p30多肽之间的抗原差异。

Antigenic differences among multiply charged Moloney murine leukemia virus p30 polypeptides found inside infected cells.

作者信息

Ikuta K, Luftig R B

出版信息

Virus Res. 1986 Nov;6(2):101-8. doi: 10.1016/0168-1702(86)90042-0.

Abstract

At least three Moloney murine leukemia virus (M-MuLV) p30 polypeptides (p30's), viz., a major species at pI 6.3 and two minor ones at pI 6.1 and pI 6.6, have previously been identified in purified virions by 2-dimensional gel electrophoresis and chromatofocusing (Katoh, I., Yoshinaka, Y. and Luftig, R.B. (1984) J. Gen. Virol. 65, 733-741). We have observed a similar, but distinctive pI pattern for [35S]methionine-labeled MuLV p30's in lysates from chronically infected (MuLV) cells. The variation in pI pattern of the intracellular MuLV p30's was dependent on the type of p30 reactive antibody used for immunoprecipitation. Specifically: a p30 spot with pI 6.3 was always precipitated as the major spot with three different antibodies, minor spots with pI 6.0 and 6.6 were variably seen dependent on the antibody used, and an intracellular p30 spot at pI 6.1 was only precipitated with a rat p30 monoclonal antibody but not with monospecific mouse or intact MuLV cross-reacting p30 sera. These results indicate that first, there are differences between the pI pattern of virion and intracellular MuLV p30's, and second, the antigenic determinants of intracellular p30's vary dependent on the antibody used for immunoprecipitation.

摘要

此前,通过二维凝胶电泳和层析聚焦法已在纯化病毒粒子中鉴定出至少三种莫洛尼鼠白血病病毒(M-MuLV)p30多肽(p30),即等电点为6.3的主要种类以及等电点为6.1和6.6的两种次要种类(加藤一、吉中义、卢夫蒂格·R·B.(1984年)《普通病毒学杂志》65卷,733 - 741页)。我们在慢性感染(MuLV)细胞的裂解物中观察到了经[35S]甲硫氨酸标记的MuLV p30呈现出类似但独特的等电点模式。细胞内MuLV p30等电点模式的变化取决于用于免疫沉淀的p30反应性抗体的类型。具体而言:等电点为6.3的p30斑点始终作为主要斑点被三种不同抗体沉淀,等电点为6.0和6.6的次要斑点是否出现则取决于所使用的抗体,并且细胞内等电点为6.1的p30斑点仅能用大鼠p30单克隆抗体沉淀,而不能用单特异性小鼠或完整MuLV交叉反应性p30血清沉淀。这些结果表明,第一,病毒粒子和细胞内MuLV p30的等电点模式存在差异;第二,细胞内p30的抗原决定簇因用于免疫沉淀的抗体不同而有所变化。

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