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布氏布氏锥虫变异特异性表面抗原信使核糖核酸的免疫纯化及部分特性分析

Immunological purification and partial characterization of variant-specific surface antigen messenger RNA of Trypanosoma brucei brucei.

作者信息

Lheureux M, Lheureux M, Vervoort T, Van Meirvenne N, Steinert M

出版信息

Nucleic Acids Res. 1979 Oct 10;7(3):595-609. doi: 10.1093/nar/7.3.595.

Abstract

Polyadenylated RNA isolated from total polyribosomes of two variable antigen types (VATs) of T. brucei brucei were shown to program the synthesis, in mRNA-dependant reticulocyte lysates, of a wide variety of polypeptides. After immunoprecipitation of these cell-free products with an homologous antiserum raised against purified variant-specific surface antigen (VSSA), a major electrophoretic band was apparent on fluorography. It was confirmed that this band corresponds to the variable antigen since only an excess of purified homologous antigen will provoke competition. The apparent molecular weight of the in vitro synthesized antigen is about 63,000 daltons. The VSSA mRNA has been found in membrane-bound polyribosomes and a 15 fold immunological purification of this mRNA has been obtained, using partially purified anti-VSSA IgG in conjunction with inactivated Staphylococcus aureus.

摘要

从布氏布氏锥虫两种可变抗原类型(VATs)的总多核糖体中分离出的聚腺苷酸化RNA,在依赖mRNA的网织红细胞裂解物中能够指导合成多种多肽。用针对纯化的变异特异性表面抗原(VSSA)产生的同源抗血清对这些无细胞产物进行免疫沉淀后,荧光自显影片上出现一条主要的电泳带。经证实,这条带对应于可变抗原,因为只有过量的纯化同源抗原才会引发竞争。体外合成抗原的表观分子量约为63,000道尔顿。已在膜结合多核糖体中发现VSSA mRNA,并使用部分纯化的抗VSSA IgG结合灭活的金黄色葡萄球菌对该mRNA进行了15倍的免疫纯化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5577/328041/7e67bdb93076/nar00456-0063-a.jpg

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