跨膜生长素进口源的异源表达:生长素转运体功能分析的意义。

International journal of plant genomics Pub Date : 2009-01-01 Epub Date: 2009-06-18 DOI:10.1155/2009/848145
David John Carrier, Norliza Tendot Abu Bakar, Karen Lawler, James Matthew Dorrian, Ameena Haider, Malcolm John Bennett, Ian Derek Kerr
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引用次数: 4

摘要

由于多种植物生长素转运体和生长素相互作用蛋白的存在,使植物体内生长素转运体的生化研究变得困难。此外,大多数此类转运体在植物中的表达水平可能太低,无法进行纯化和下游功能分析。异源表达系统应该解决这两个问题。我们已经研究了许多这样的系统在拟南芥中表达AUX1的效率。我们发现基于重组杆状病毒感染昆虫细胞的真核系统提供了一个高水平、易于扩展的表达系统,能够提供对AUX1的功能检测。此外,哺乳动物细胞中的瞬时转染系统可以研究AUX1的定位和AUX1介导的生长素运输。相比之下,我们无法利用P. pastoris或L. lactis表达系统来可靠地表达AUX1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Heterologous expression of a membrane-spanning auxin importer: implications for functional analyses of auxin transporters.

Biochemical studies of plant auxin transporters in vivo are made difficult by the presence of multiple auxin transporters and auxin-interacting proteins. Furthermore, the expression level of most such transporters in plants is likely to be too low for purification and downstream functional analysis. Heterologous expression systems should address both of these issues. We have examined a number of such systems for their efficiency in expressing AUX1 from Arabidopsis thaliana. We find that a eukaryotic system based upon infection of insect cells with recombinant baculovirus provides a high level, easily scalable expression system capable of delivering a functional assay for AUX1. Furthermore, a transient transfection system in mammalian cells enables localization of AUX1 and AUX1-mediated transport of auxin to be investigated. In contrast, we were unable to utilise P. pastoris or L. lactis expression systems to reliably express AUX1.

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