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本文引用的文献

1
Cooperativity and allostery in aquaporin 0 regulation by Ca.钙对水通道蛋白 0 调节的协同作用和别构调节
Biochim Biophys Acta Biomembr. 2019 May 1;1861(5):988-996. doi: 10.1016/j.bbamem.2019.02.007. Epub 2019 Feb 22.
2
Aquaglyceroporin PbAQP is required for efficient progression through the liver stage of Plasmodium infection.水甘油通道蛋白 PbAQP 是疟原虫感染肝脏阶段有效进展所必需的。
Sci Rep. 2018 Jan 12;8(1):655. doi: 10.1038/s41598-017-18987-3.
3
Computing osmotic permeabilities of aquaporins AQP4, AQP5, and GlpF from near-equilibrium simulations.从近平衡模拟计算水通道蛋白 AQP4、AQP5 和 GlpF 的渗透系数。
Biochim Biophys Acta Biomembr. 2017 Aug;1859(8):1310-1316. doi: 10.1016/j.bbamem.2017.04.022. Epub 2017 Apr 25.
4
Mammalian aquaglyceroporin function in metabolism.哺乳动物水甘油通道蛋白在新陈代谢中的功能。
Biochim Biophys Acta. 2016 Jan;1858(1):1-11. doi: 10.1016/j.bbamem.2015.10.004. Epub 2015 Oct 9.
5
Erythritol predicted to inhibit permeation of water and solutes through the conducting pore of P. falciparum aquaporin.赤藓糖醇预计可抑制水和溶质通过恶性疟原虫水通道蛋白的传导孔渗透。
Biophys Chem. 2015 Mar;198:14-21. doi: 10.1016/j.bpc.2015.01.004. Epub 2015 Jan 14.
6
SWISS-MODEL: modelling protein tertiary and quaternary structure using evolutionary information.SWISS-MODEL:利用进化信息进行蛋白质三级和四级结构建模。
Nucleic Acids Res. 2014 Jul;42(Web Server issue):W252-8. doi: 10.1093/nar/gku340. Epub 2014 Apr 29.
7
Aquaporins: important but elusive drug targets.水通道蛋白:重要但难以捉摸的药物靶点。
Nat Rev Drug Discov. 2014 Apr;13(4):259-77. doi: 10.1038/nrd4226. Epub 2014 Mar 14.
8
Structural determinants of the hydrogen peroxide permeability of aquaporins.水通道蛋白过氧化氢通透性的结构决定因素。
FEBS J. 2014 Feb;281(3):647-56. doi: 10.1111/febs.12653. Epub 2013 Dec 13.
9
Parasite aquaporins: current developments in drug facilitation and resistance.寄生虫水通道蛋白:药物促进与耐药性的当前进展
Biochim Biophys Acta. 2014 May;1840(5):1566-73. doi: 10.1016/j.bbagen.2013.10.014. Epub 2013 Oct 17.
10
Glycerol modulates water permeation through Escherichia coli aquaglyceroporin GlpF.甘油调节水通过大肠杆菌水甘油通道蛋白GlpF的渗透。
Biochim Biophys Acta. 2013 Aug;1828(8):1786-93. doi: 10.1016/j.bbamem.2013.03.008. Epub 2013 Mar 16.

布朗动力学涨落耗散定理在伯氏疟原虫转运蛋白PbAQP研究中的应用。

Application of the Brown dynamics fluctuation-dissipation theorem to the study of Plasmodium berghei transporter protein PbAQP.

作者信息

Chen Liao Y

机构信息

Department of Physics and Astronomy, The University of Texas at San Antonio, San Antonio, Texas, USA.

出版信息

Front Phys. 2020 Apr;8. doi: 10.3389/fphy.2020.00119. Epub 2020 Apr 17.

DOI:10.3389/fphy.2020.00119
PMID:32457897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7250396/
Abstract

In this article, the Brownian dynamics fluctuation-dissipation theorem (BD-FDT) is applied to the study of transport of neutral solutes across the cellular membrane of Plasmodium berghei (Pb), a disease-causing parasite. Pb infects rodents and causes symptoms in laboratory mice that are comparable to human malaria caused by Plasmodium falciparum (Pf). Due to the relative ease of its genetic engineering, P. berghei has been exploited as a model organism for the study of human malaria. P. berghei expresses one type of aquaporin (AQP), PbAQP, and, in parallel, P. falciparum expresses PfAQP. Either PbAQP or PfAQP is a multifunctional channel protein in the plasma membrane of the rodent/human malarial parasite for homeostasis of water, uptake of glycerol, and excretion of some metabolic wastes across the cell membrane. This FDT-study of the channel protein PbAQP is to elucidate how and how strongly it interacts with water, glycerol, and erythritol. It is found that erythritol, which binds deep inside the conducting pore of PbAQP/PfAQP, inhibits the channel protein's functions of conducting water, glycerol . This points to the possibility that erythritol, a sugar substitute, may inhibit the malarial parasites in rodents and in humans.

摘要

在本文中,布朗动力学涨落耗散定理(BD-FDT)被应用于研究中性溶质跨致病寄生虫伯氏疟原虫(Pb)细胞膜的转运。伯氏疟原虫感染啮齿动物,并在实验室小鼠中引发与恶性疟原虫(Pf)引起的人类疟疾相当的症状。由于其基因工程相对容易操作,伯氏疟原虫已被用作研究人类疟疾的模式生物。伯氏疟原虫表达一种水通道蛋白(AQP),即PbAQP,同时,恶性疟原虫表达PfAQP。PbAQP或PfAQP都是啮齿动物/人类疟原虫质膜中的多功能通道蛋白,用于维持水的稳态、摄取甘油以及跨细胞膜排泄一些代谢废物。对通道蛋白PbAQP的这项基于涨落耗散定理的研究旨在阐明它如何以及在多大程度上与水、甘油和赤藓糖醇相互作用。研究发现,结合在PbAQP/PfAQP传导孔深处的赤藓糖醇会抑制通道蛋白传导水、甘油的功能。这表明糖替代品赤藓糖醇可能抑制啮齿动物和人类体内疟原虫的可能性。