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测量酵母中质膜和液泡转运蛋白的活性

Measuring the Activity of Plasma Membrane and Vacuolar Transporters in Yeast.

作者信息

Cools Melody, Rompf Maria, Mayer Andreas, André Bruno

机构信息

Molecular Physiology of the Cell, Université Libre de Bruxelles (ULB), Biopark, Belgium.

Department of Biochemistry, University of Lausanne (UNIL), Lausanne, Switzerland.

出版信息

Methods Mol Biol. 2019;2049:247-261. doi: 10.1007/978-1-4939-9736-7_15.

Abstract

The yeast proteome includes about 300 polytopic membrane proteins known or predicted to function as transporters. Such proteins ensure active or passive transport of small ions or metabolites across the plasma or internal membranes. Despite decades of research on yeast transporters, many of these remain uncharacterized in terms of substrate selectivity range, subcellular localization, and biological function. Assaying the uptake of radiolabeled compounds into whole cells or isolated organelles remains a powerful method for characterizing the function and biochemical properties of these proteins. Here we describe established protocols for measuring transporter activity in whole cells, intact vacuoles, or reconstituted vacuolar vesicles. These methods have proved particularly useful in the context of our work on yeast amino acid transporters, and can in principle be applied to assaying the uptake of other categories of compounds.

摘要

酵母蛋白质组包含约300种已知或预测具有转运功能的多跨膜蛋白。这类蛋白质确保小离子或代谢物在质膜或内膜上的主动或被动运输。尽管对酵母转运蛋白进行了数十年的研究,但其中许多在底物选择性范围、亚细胞定位和生物学功能方面仍未得到表征。检测放射性标记化合物进入全细胞或分离细胞器的摄取情况仍然是表征这些蛋白质功能和生化特性的有力方法。在这里,我们描述了用于测量全细胞、完整液泡或重组液泡膜泡中转运蛋白活性的既定方案。这些方法在我们对酵母氨基酸转运蛋白的研究中已证明特别有用,并且原则上可应用于检测其他类化合物的摄取。

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