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Comparative transport efficiencies of urea analogues through urea transporter UT-B

机译:尿素类似物通过尿素转运蛋白UT-B的比较转运效率

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Expression of urea transporter UT-B confers high urea permeability to mammalian erythrocytes. Erythrocyte membranes also permeate various urea analogues, suggesting common transport pathways for urea and structurally similar solutes. In this study, we examined UT-B-facilitated passage of urea analogues and other neutral small solutes by comparing transport properties of wildtype to UT-B-deficient mouse erythrocytes. Stopped-flow light-scattering measurements indicated high UT-B permeability to urea and chemical analogues formamide, acetamide, methylurea, methylformarnide, ammonium carbarnate, and acrylamide, each with P-s > 5.0 x 10(-6) cm/s at 10 degrees C. UT-B genetic knockout and phloretin treatment of wildtype erythrocytes similarly reduced urea analogue permeabilities. Strong temperature dependencies of formamide, acetamide, acrylamide and butyramide transport across UT-B-null membranes (E-a > 10 kcal/mol) suggested efficient diffusion of these amides across lipid bilayers. Urea analogues dimethylurea, acryalmide, methylurea, thiourea and methylformamide inhibited UT-B-mediated urea transport by > 60% in the absence of transmembrane analogue gradients, supporting a pore-blocking mechanism of UT-B inhibition. Differential transport efficiencies of urea and its analogues through UT-B provide insight into chemical interactions between neutral solutes and the UT-B pore. (c) 2007 Elsevier B.V. All rights reserved.
机译:尿素转运蛋白UT-B的表达赋予哺乳动物红细胞高尿素渗透性。红细胞膜也渗透到各种尿素类似物中,提示尿素和结构相似的溶质具有共同的转运途径。在这项研究中,我们通过比较野生型与UT-B缺陷型小鼠红细胞的转运特性,研究了UT-B促进的尿素类似物和其他中性小溶质的传递。停止流动的光散射测量表明,UT-B对尿素和化学类似物甲酰胺,乙酰胺,甲基脲,甲基甲酰胺,氨基甲酸铵和丙烯酰胺具有很高的UT-B渗透性,在10摄氏度时Ps> 5.0 x 10(-6)cm / s UT-B基因敲除和促黄体素处理野生型红细胞同样降低了尿素类似物的通透性。甲酰胺,乙酰胺,丙烯酰胺和丁酰胺在UT-B空膜上的转运(E-a> 10 kcal / mol)对温度的强烈依赖性表明这些酰胺在脂质双层中的有效扩散。在不存在跨膜类似物梯度的情况下,尿素类似物二甲基脲,丙烯酰胺,甲基脲,硫脲和甲基甲酰胺可将UT-B介导的尿素转运抑制> 60%,从而支持UT-B抑制的孔隙阻断机制。尿素及其类似物通过UT-B的差异传输效率提供了对中性溶质与UT-B孔之间化学相互作用的了解。 (c)2007 Elsevier B.V.保留所有权利。

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