Suppr超能文献

重组纤连蛋白多肽的高效稳定表达。

Efficient and stable expression of recombinant fibronectin polypeptides.

作者信息

Schwarzbauer J E, Mulligan R C, Hynes R O

出版信息

Proc Natl Acad Sci U S A. 1987 Feb;84(3):754-8. doi: 10.1073/pnas.84.3.754.

Abstract

We describe retroviral expression vectors containing cDNAs encoding part of fibronectin preceded by the signal and "pro" sequences of parathyroid hormone. The recombinant retroviruses were used to generate NIH 3T3 cell lines stably producing functionally active fragments of fibronectin. The recombinant fibronectins (deminectins) are processed and secreted by the cells and form disulfide-bonded dimers with themselves and with endogenous fibronectin subunits. The fibronectin-deminectin heterodimers are incorporated into the extracellular matrix. We describe cell lines producing six variant forms of deminectin corresponding to variant forms of fibronectin produced by alternative splicing. In constructing fibronectin cDNAs encoding the six variant forms, we also made use of the ability of retroviral vectors to generate cDNAs by accurate splicing of cloned genomic segments. These constructs should be valuable in analyses of the structure-function relationships of fibronectins.

摘要

我们描述了逆转录病毒表达载体,其包含编码纤连蛋白部分的cDNA,该cDNA之前有甲状旁腺激素的信号序列和“前体”序列。重组逆转录病毒用于生成稳定产生具有功能活性的纤连蛋白片段的NIH 3T3细胞系。重组纤连蛋白(去纤连蛋白)由细胞加工并分泌,并与自身以及内源性纤连蛋白亚基形成二硫键连接的二聚体。纤连蛋白-去纤连蛋白异源二聚体被整合到细胞外基质中。我们描述了产生六种去纤连蛋白变体形式的细胞系,这些变体形式对应于通过可变剪接产生的纤连蛋白变体形式。在构建编码这六种变体形式的纤连蛋白cDNA时,我们还利用了逆转录病毒载体通过对克隆的基因组片段进行精确剪接来生成cDNA的能力。这些构建体在纤连蛋白结构-功能关系的分析中应具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8364/304294/23901434db72/pnas00268-0148-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验