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生物素在大鼠肝脏基底外侧膜囊泡中的转运

Transport of biotin in basolateral membrane vesicles of rat liver.

作者信息

Said H M, Korchid S, Horne D W, Howard M

机构信息

Department of Medicine, University of California School of Medicine, Irvine 92717.

出版信息

Am J Physiol. 1990 Nov;259(5 Pt 1):G865-72. doi: 10.1152/ajpgi.1990.259.5.G865.

DOI:10.1152/ajpgi.1990.259.5.G865
PMID:2240226
Abstract

We examined biotin transport across the basolateral membrane (BLM) of rat liver using BLM vesicles (BLMV) technique. The purity and suitability for transport studies of liver BLMV were demonstrated by morphological (electron microscopy), enzymatic, and functional criteria. Orientation of liver BLMV was determined by freeze-fracture electron microscopy and by [3H]ouabain binding methodology and was found to be 65.3-69.7% in the right-side-out orientation. Uptake of biotin by liver BLMV was found by osmolarity and temperature studies to be mostly the result of transport of the substrate into an active intravesicular space with little binding to membrane surfaces. Transport of biotin was found to be Na+ gradient dependent with a distinct "over-shoot" phenomenon. Initial rate of transport of biotin as a function of concentration was found to include a saturable component in the presence of a Na+ gradient (out greater than in) but was linear and lower in the presence of a K+ gradient (no Na+). Kinetic parameters of the saturable Na+ gradient-dependent transport process were 0.39 microM and 1,807 fmol.mg protein-1.20 s-1 for the apparent Km and Vmax, respectively. In the presence, but not the absence, of a Na+ gradient (out greater than in), the addition of structural analogues to the incubation medium caused significant inhibition in the transport of 0.079 microM [3H]biotin. Induction, with the use of valinomycin and an inwardly directed K+ gradient, of a relatively positive intravesicular space caused significant inhibition in the initial rate of biotin transport.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们采用基底外侧膜囊泡(BLMV)技术研究了生物素跨大鼠肝脏基底外侧膜(BLM)的转运。通过形态学(电子显微镜)、酶学和功能标准证明了肝脏BLMV的纯度及其适用于转运研究。通过冷冻断裂电子显微镜和[3H]哇巴因结合方法确定了肝脏BLMV的取向,发现右侧向外取向的比例为65.3 - 69.7%。通过渗透压和温度研究发现,肝脏BLMV对生物素的摄取主要是底物转运到活跃的囊泡内空间的结果,与膜表面的结合很少。发现生物素的转运依赖于Na +梯度,存在明显的“过冲”现象。发现生物素的初始转运速率作为浓度的函数,在存在Na +梯度(外大于内)时包括一个可饱和成分,但在存在K +梯度(无Na +)时是线性的且较低。可饱和的Na +梯度依赖性转运过程的动力学参数,表观Km和Vmax分别为0.39 microM和1,807 fmol·mg蛋白-1·20 s-1。在存在(而非不存在)Na +梯度(外大于内)的情况下,向孵育培养基中添加结构类似物会显著抑制0.079 microM [3H]生物素的转运。使用缬氨霉素和内向的K +梯度诱导相对正的囊泡内空间,会显著抑制生物素转运的初始速率。(摘要截短于250字)

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