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人水通道蛋白在毕赤酵母中的重组生产(特邀综述)

Recombinant production of the human aquaporins in the yeast Pichia pastoris (Invited Review).

作者信息

Oberg Fredrik, Hedfalk Kristina

机构信息

Department of Chemistry and Molecular Biology, University of Gothenburg, Sweden.

出版信息

Mol Membr Biol. 2013 Feb;30(1):15-31. doi: 10.3109/09687688.2012.665503. Epub 2012 Aug 21.

Abstract

Aquaporins are water facilitating proteins embedded in the cellular membranes. Such channels have been identified in almost every living organism - including humans. These proteins are vital molecules and their malfunction can lead to several severe disorders and diseases. Hence, an increased understanding of their structure, function and regulation is of the utmost importance for developing current and future drugs. Heading towards this goal, the first problem to overcome is to acquire the proteins in sufficient amounts to enable functional and structural characterization. Using a suitable host organism, large amounts of target molecules can possibly be produced, but for membrane proteins limitations are frequently encountered. In the work described here, we have produced the 13 human aquaporins (hAQPs) in one of the most successful hosts for recombinant overproduction of eukaryotic proteins; the yeast Pichia pastoris, in order to explore the underlying bottleneck to a successful membrane protein production experiment. Here we present exceptional yield of hAQP1, whereas some other hAQPs were below the threshold needed for scaled up production. In the overproduction process, we have established methods for efficient production screening as well as for accurate determination of the initial production yield. Furthermore, we have optimized the yield of low producing targets, enabling studies of proteins previously out of reach, exemplified with hAQP4 as well as the homologue PfAQP. Taken together, our results. present insight into factors directing high production of eukaryotic membrane proteins together with suggestions on ways to optimize the recombinant production in the yeast P. pastoris.

摘要

水通道蛋白是嵌入细胞膜中的促进水运输的蛋白质。几乎在包括人类在内的每一种生物中都发现了这类通道。这些蛋白质是至关重要的分子,其功能失调会导致多种严重的病症和疾病。因此,深入了解它们的结构、功能和调节对于开发当前及未来的药物至关重要。为了实现这一目标,首先要克服的问题是获得足够数量的蛋白质,以便进行功能和结构表征。利用合适的宿主生物,有可能大量生产目标分子,但对于膜蛋白来说,经常会遇到限制。在本文所述的工作中,我们在用于真核蛋白重组过量表达最成功的宿主之一——酵母毕赤酵母中生产了13种人类水通道蛋白(hAQP),以探究成功进行膜蛋白生产实验的潜在瓶颈。在此我们展示了hAQP1的超高产量,而其他一些hAQP产量低于扩大生产所需的阈值。在过量生产过程中,我们建立了高效生产筛选方法以及准确测定初始产量的方法。此外,我们优化了低产量目标蛋白的产量,使得以前无法研究的蛋白质能够进行研究,以hAQP4以及同源物PfAQP为例。综上所述,我们的结果揭示了指导真核膜蛋白高产的因素,并提出了优化酵母毕赤酵母中重组生产的方法建议。

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