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从布氏锥虫血液和培养形式中分离的RNA在无细胞网织红细胞系统中的翻译。

Translation in a reticulocyte cell-free system of RNA isolated from blood and culture forms of Trypanosoma brucei.

作者信息

Eggitt M J, Tappenden L, Brown K N

出版信息

Parasitology. 1977 Oct;75(2):133-41. doi: 10.1017/s0031182000062272.

Abstract

RNA with messenger activity has been extracted from both blood and culture (insect mid-gut) forms of Trypanosoma brucei and translated in a reticulocyte cell-free system. The products of this cell-free system have been compared, and many common polypeptides demonstrated. A major polypeptide of 58000--65000 molecular weight was made when both blood and culture form RNA was added to the cell-free system. Antiserum raised against purified variant antigen from a cloned variant (MIAG 099) was used to detect specific products of this system. A major polypeptide of approximately 58000-65000 molecular weight was precipitated when the homologous trypanosome (MIAG 099) blood form RNA was used in the cell-free system. No such polypeptide was precipitated when RNA from a heterologous strain culture or blood form was used in the system. Competition experiments, in which excess purified variant antigen was addded after incubation but before addition of specific antiserum, confirmed that the polypeptide of 58000--65000 molecular weight is the variant antigen.

摘要

已从布氏锥虫的血液和培养(昆虫中肠)形态中提取出具有信使活性的RNA,并在网织红细胞无细胞系统中进行翻译。对该无细胞系统的产物进行了比较,发现了许多共同的多肽。当将血液和培养形态的RNA都添加到无细胞系统中时,会产生一种分子量为58000 - 65000的主要多肽。用针对克隆变体(MIAG 099)纯化的变体抗原产生的抗血清来检测该系统的特定产物。当在无细胞系统中使用同源锥虫(MIAG 099)血液形态的RNA时,一种分子量约为58000 - 65000的主要多肽会沉淀下来。当在该系统中使用来自异源菌株培养物或血液形态的RNA时,不会沉淀出这样的多肽。在孵育后但在添加特异性抗血清之前添加过量纯化变体抗原的竞争实验证实,分子量为58000 - 65000的多肽就是变体抗原。

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