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肠道刷状缘脯氨酸转运的特异性:花青染料研究

Specificity of intestinal brush-border proline transport: cyanine dye studies.

作者信息

Wright E M, Schell R E, Stevens B R

出版信息

Biochim Biophys Acta. 1985 Aug 27;818(2):271-4. doi: 10.1016/0005-2736(85)90568-1.

Abstract

The ability of rabbit jejunal brush borders to transport inhibitors of the imino carrier was investigated in membrane vesicles by measuring their ability to depolarize the membrane potential. Membrane potentials were monitored using a voltage-sensitive cyanine dye. Piperidine and pyrrolidine carboxylic acids, which are potent inhibitors of Na+-dependent proline transport (Ki less than 0.5 mM) depolarize the potential in a Na+-dependent, saturable manner indicating transport. On the other hand, N-methylated amino acids, which are fair inhibitors (Ki 2-10 mM), do not depolarize the membrane to any significant extent, but they competitively inhibit the L-proline transport signal. This indicates that these analogs are nontransported inhibitors of the imino carrier. The poor inhibitors niacin and pipolinic acid (Ki greater than 60 mM) depolarize the membrane about twice as much as proline and with low Kf values. This suggests separate carriers for these substrates.

摘要

通过测量兔空肠刷状缘膜囊泡使膜电位去极化的能力,研究了其转运亚氨基载体抑制剂的能力。使用电压敏感染料监测膜电位。哌啶和吡咯烷羧酸是Na⁺依赖性脯氨酸转运的强效抑制剂(Ki小于0.5 mM),它们以Na⁺依赖性、可饱和的方式使电位去极化,表明发生了转运。另一方面,N-甲基化氨基酸是中等抑制剂(Ki为2 - 10 mM),在任何显著程度上都不会使膜去极化,但它们竞争性抑制L-脯氨酸转运信号。这表明这些类似物是亚氨基载体的非转运抑制剂。弱抑制剂烟酸和哌啶酸(Ki大于60 mM)使膜去极化的程度约为脯氨酸的两倍,且Kf值较低。这表明这些底物有不同的载体。

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