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丝状真菌中的转运实验:构巢曲霉 UapC 嘌呤转运蛋白的动力学特征。

Transport assays in filamentous fungi: kinetic characterization of the UapC purine transporter of Aspergillus nidulans.

机构信息

Faculty of Biology, University of Athens, Panepistimioupolis, Athens 15784, Greece.

Faculty of Biology, University of Athens, Panepistimioupolis, Athens 15784, Greece.

出版信息

Fungal Genet Biol. 2014 Feb;63:1-8. doi: 10.1016/j.fgb.2013.12.004. Epub 2013 Dec 16.

Abstract

Transport assays allow the direct kinetic analysis of a specific transporter by measuring apparent Km and Vmax values, and permit the characterization of substrate specificity profiles through competition assays. In this protocol we describe a rapid and easy method for performing uptake assays in the model filamentous ascomycete Aspergillus nidulans. Our method makes use of A. nidulans germinating conidiospores at a defined morphological stage in which most transporters show maximal expression, avoiding technical difficulties associated with the use of mycelia. In combination with the ease of construction of genetic null mutants in A. nidulans, our method allows the rigorous characterization of any transporter in genetic backgrounds that are devoid of other transporters of similar specificity. Here, we use this method to characterize the kinetic parameters and the specificity profile of UapC, a uric acid-xanthine transporter present in all ascomycetes and member of the ubiquitous Nucleobase-Ascorbate Transporter family, in specific genetic backgrounds lacking other relevant transporters.

摘要

转运蛋白分析可通过测量表观 Km 和 Vmax 值,直接对特定转运蛋白进行动力学分析,并通过竞争分析来描述底物特异性特征。在本方案中,我们描述了一种在丝状子囊菌构巢曲霉中进行摄取分析的快速简便方法。我们的方法利用构巢曲霉处于特定形态发生阶段的萌发分生孢子,在此阶段大多数转运蛋白表达达到最大值,从而避免了使用菌丝体所带来的技术难题。与在缺乏类似特异性转运蛋白的遗传背景中构建基因缺失突变体的简易性相结合,我们的方法允许对任何转运蛋白进行严格的特征描述。在这里,我们使用该方法在缺乏其他相关转运蛋白的特定遗传背景下,对尿酸-黄嘌呤转运蛋白 UapC 的动力学参数和特异性特征进行了表征。UapC 存在于所有子囊菌中,是普遍存在的核苷酸碱基-抗坏血酸转运蛋白家族的成员。

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