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干扰素诱导的15 kDa蛋白的分子特征。分子克隆及核苷酸和氨基酸序列。

Molecular characterization of the interferon-induced 15-kDa protein. Molecular cloning and nucleotide and amino acid sequence.

作者信息

Blomstrom D C, Fahey D, Kutny R, Korant B D, Knight E

出版信息

J Biol Chem. 1986 Jul 5;261(19):8811-6.

PMID:3087979
Abstract

We have isolated a cDNA clone for an interferon-induced 15-kDa protein. The cDNA clone was prepared from mRNA isolated from interferon-beta-treated human Daudi cells. The clone of 635 base pairs contains an open reading frame coding for a protein of 145 amino acids, and suggests for the mRNA a 75-base pair 5' untranslated and a 125-base pair 3' untranslated region. Approximately 85% of the amino acid sequence of the 15-kDa protein has been independently obtained from 2 nmol of material using microsequencing technology on the N terminus of the intact protein and on tryptic and chymotryptic peptides. The amino acid sequence of the isolated protein is identical to the amino acid sequence deduced from the cDNA. Northern blot analysis confirmed that the mRNA for the 15-kDa protein is undetectable in untreated cells, but is greatly induced following interferon treatment.

摘要

我们分离出了一种干扰素诱导的15 kDa蛋白的cDNA克隆。该cDNA克隆是从经β干扰素处理的人Daudi细胞中分离出的mRNA制备而来的。这个635个碱基对的克隆包含一个编码145个氨基酸的开放阅读框,并显示该mRNA有一个75个碱基对的5'非翻译区和一个125个碱基对的3'非翻译区。使用微量测序技术,已从2 nmol完整蛋白质的N端以及胰蛋白酶和糜蛋白酶肽段中独立获得了该15 kDa蛋白约85%的氨基酸序列。分离出的蛋白质的氨基酸序列与从cDNA推导的氨基酸序列相同。Northern印迹分析证实,在未处理的细胞中检测不到15 kDa蛋白的mRNA,但在干扰素处理后会大量诱导产生。

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