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血清素转运体-丙咪嗪“受体”

The serotonin transporter-imipramine "receptor".

作者信息

Talvenheimo J, Fishkes H, Nelson P J, Rudnick G

出版信息

J Biol Chem. 1983 May 25;258(10):6115-9.

PMID:6853478
Abstract

The platelet plasma membrane serotonin transporter requires Na+ for two reactions, serotonin transport and imipramine binding. Although imipramine binding has been thought to reflect the same process required for serotonin binding prior to transport (Talvenheimo, J., Nelson, P.J., and Rudnick, G. (1979) J. Biol. Chem. 254, 4631-4635), binding and transport display markedly different responses to Na+. Imipramine binding (and competitive inhibition of transport) apparently requires two sodium ions which bind with a KD of 300 +/- 70 meq/liter. The total number of sites (Bmax) is the same at all Na+ concentrations, but the affinity for imipramine increases from 7.3 x 10(6) M-1 at 20 meq/liter to 110 x 10(6) M-1 at 200 meq/liter. Na+ acts, at least in part, by decreasing the rate of imipramine dissociation from its binding site. Serotonin binding displaces imipramine from its site on the membrane. In contrast to imipramine binding, this displacement is a simple, hyperbolic function of Na+ concentration with a KD for Na+ of 400 +/- 100 meq/liter, which suggests that only one Na+ is required. Serotonin transport is also much less responsive to Na+ concentration. Over the same concentration range in which the affinity for imipramine increases 15-fold, the affinity for serotonin increases only 2-fold. Despite the lack of Na+ effect on the Bmax for imipramine binding, the Vmax for serotonin transport increases as a simple saturable function of Na+ with a KM (Na+) of 52 meq/liter. Thus, substrate translocation as well as binding requires Na+. Since serotonin is cotransported with Na+, the serotonin gradient accumulated depends on the coupling stoichiometry and the magnitude of the Na+ gradient imposed. From the response of the serotonin gradient to imposed Na+ gradients, we calculated a serotonin:Na+ cotransport stoichiometry of 0.9. Taken together, the results suggest that serotonin and imipramine bind either to the same site or to mutually exclusive sites, but maximal imipramine binding requires two sodium ions, while maximal serotonin binding and translocation requires only one.

摘要

血小板质膜5-羟色胺转运体在两种反应中需要Na⁺,即5-羟色胺转运和丙咪嗪结合。虽然丙咪嗪结合一直被认为反映了5-羟色胺在转运前结合所需的相同过程(塔尔文海莫,J.,尼尔森,P.J.,和鲁德尼克,G.(1979年)《生物化学杂志》254,4631 - 4635),但结合和转运对Na⁺的反应明显不同。丙咪嗪结合(以及对转运的竞争性抑制)显然需要两个钠离子,其结合的解离常数KD为300±70毫当量/升。在所有Na⁺浓度下,位点总数(Bmax)相同,但丙咪嗪的亲和力从20毫当量/升时的7.3×10⁶M⁻¹增加到200毫当量/升时的110×10⁶M⁻¹。Na⁺至少部分通过降低丙咪嗪从其结合位点的解离速率起作用。5-羟色胺结合会将丙咪嗪从其在膜上的位点置换下来。与丙咪嗪结合相反,这种置换是Na⁺浓度的简单双曲线函数,Na⁺的KD为400±100毫当量/升,这表明只需要一个Na⁺。5-羟色胺转运对Na⁺浓度的反应也小得多。在丙咪嗪亲和力增加15倍的相同浓度范围内,5-羟色胺的亲和力仅增加2倍。尽管Na⁺对丙咪嗪结合的Bmax没有影响,但5-羟色胺转运的Vmax随着Na⁺的简单饱和函数增加,其米氏常数(Km[Na⁺])为52毫当量/升。因此,底物转运以及结合都需要Na⁺。由于5-羟色胺与Na⁺协同转运,积累的5-羟色胺梯度取决于偶联化学计量和施加的Na⁺梯度的大小。根据5-羟色胺梯度对施加的Na⁺梯度的反应,我们计算出5-羟色胺:Na⁺协同转运化学计量为0.9。综上所述,结果表明5-羟色胺和丙咪嗪要么结合到同一位点,要么结合到互斥位点,但最大丙咪嗪结合需要两个钠离子,而最大5-羟色胺结合和转运只需要一个。

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