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用于研究人类溶酶体胱氨酸转运蛋白胱氨酸酶的基因筛选。

A Genetic Screen for Investigating the Human Lysosomal CystineTransporter, Cystinosin.

机构信息

Indian Institute of Science and Education Research Mohali, Sector 81, Knowledge City, SAS Nagar, Punjab, India.

出版信息

Sci Rep. 2018 Feb 21;8(1):3442. doi: 10.1038/s41598-018-21483-x.

Abstract

Cystinosin, a lysosomal transporter is involved in the efflux of cystine from the lysosome to the cytosol. Mutations in the human cystinosin gene (CTNS) cause cystinosis, a recessive autosomal disorder. Studies on cystinosin have been limited by the absence of a robust genetic screen. In the present study we have developed a dual strategy for evaluating cystinosin function that is amenable to rapid genetic analysis. We show that human cystinosin expressed in this yeast confers growth on cystine when the protein is mistargeted to the plasma membrane by the deletion of the C-terminal targeting signal, GYQDL. We also screened a vacuolar protein sorting deletion library, and subsequently created multiple vps deletion mutants for kinetic studies. The double deletion, vps1Δvps17Δ, greatly enhanced uptake. This enabled validation by kinetic studies, including first studies on the WT CTNS protein (that contained the GYQDL motif). Using this screen we isolated several gain of function mutants, G131S/D, G309S/D, A137V, G197R, S270T, L274F and S312N showing enhanced growth on low concentrations of cystine. Kinetic analysis yielded insights into the role of the residues (including one of the patient mutations, G197R). The results indicate that the screen could be effectively used for interrogating and understanding the CTNS protein.

摘要

半胱氨酸转运蛋白,一种溶酶体转运蛋白,参与胱氨酸从溶酶体向细胞质的外排。人类半胱氨酸转运蛋白基因 (CTNS) 的突变导致胱氨酸病,这是一种隐性常染色体疾病。对半胱氨酸转运蛋白的研究受到缺乏强大遗传筛选的限制。在本研究中,我们开发了一种评估半胱氨酸转运蛋白功能的双重策略,该策略适用于快速遗传分析。我们表明,当通过缺失 C 末端靶向信号 GYQDL 将人源半胱氨酸转运蛋白错误靶向质膜时,在酵母中表达的人源半胱氨酸转运蛋白可以在胱氨酸上生长。我们还筛选了液泡蛋白分选缺失文库,并随后创建了多个 vps 缺失突变体进行动力学研究。双缺失 vps1Δvps17Δ 极大地增强了摄取。这使通过动力学研究进行验证成为可能,包括对 WT CTNS 蛋白(含有 GYQDL 基序)的首次研究。使用该筛选,我们分离到几个获得功能的突变体,G131S/D、G309S/D、A137V、G197R、S270T、L274F 和 S312N,它们在低浓度胱氨酸下显示出增强的生长。动力学分析深入了解了这些残基的作用(包括一个患者突变 G197R)。结果表明,该筛选可以有效地用于研究和理解 CTNS 蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d0/5821828/656c0e52d2ca/41598_2018_21483_Fig1_HTML.jpg

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