The inhibition of glycerol permeation through aquaglyceroporin-3 induced by mercury(II): A molecular dynamics study

被引:24
|
作者
Spinello, Angelo [1 ,2 ]
de Almeida, Andreia [3 ]
Casini, Angela [3 ,4 ]
Barone, Giampaolo [1 ,2 ]
机构
[1] Univ Palermo, Dipartimento Sci & Tecnol Biol Chim & Farmaceut S, Viale Sci Ed 16, I-90128 Palermo, Italy
[2] Ist EuroMediterraneo Sci & Tecnol IEMEST, Via Emer Amari 123, I-90139 Palermo, Italy
[3] Univ Groningen, Groningen Res Inst Pharm, Dept Pharmacokinet Toxicol & Targeting, A Deusinglaan 1, NL-9731 AV Groningen, Netherlands
[4] Cardiff Univ, Sch Chem, Main Bldg,Pk Pl, Cardiff CF10 3AT, S Glam, Wales
关键词
Aquaglyceroporin; Glycerol permeation; Mercury; Molecular dynamics; Water permeation; WATER CHANNEL; AQUAPORIN INHIBITION; STRUCTURAL BASIS; PERMEABILITY; COMPLEXES; GLPF; CRYSTAL; CYSTEINE-189; COORDINATION; SIMULATIONS;
D O I
10.1016/j.jinorgbio.2015.11.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mercurial compounds are known to inhibit water permeation through aquaporins (AQPs). Although in the last years some hypotheses were proposed, the exact mechanism of inhibition is still an open question and even less is known about the inhibition of the glycerol permeation through aquaglyceroporins. Molecular dynamics (MD) simulations of human aquaporin-3 (AQP3) have been performed up to 200 ns in the presence of Hg2+ ions. For the first time, we have observed the unbiased passage of a glycerol molecule from the extracellular to cytosolic side. Moreover, the presence of Hg2+ ions covalently bound to Cys40 leads to a collapse of the aromatic/arginine selectivity filter (ar/R SF), blocking the passage of both glycerol and water. Interestingly, the local conformational changes of the protein follow mercury coordination by water and by aminoacidic donor atoms. Overall, the obtained results are important to improve the design of selective AQP inhibitors for future therapeutic and imaging applications. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:78 / 84
页数:7
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