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人红细胞对D-葡萄糖的预稳态摄取与循环载体机制不一致。

Pre-steady-state uptake of D-glucose by the human erythrocyte is inconsistent with a circulating carrier mechanism.

作者信息

Naftalin R J

机构信息

Department of Physiology, King's College London, U.K.

出版信息

Biochim Biophys Acta. 1988 Dec 22;946(2):431-8. doi: 10.1016/0005-2736(88)90420-8.

Abstract

Simulation shows that the four-state mobile carrier model for sugar transport in which the asymmetry arises from unequal rate constants of inward and outward translation of the free-carrier and carrier-sugar complex, does not fit with the observed data for pre-steady-state uptake recently obtained by A.G. Lowe and A.R. Walmsley [1987) Biochim. Biophys. Acta 903, 547-550). The main reason for this discrepancy is that pre-steady-state fluxes are determined mainly by the dissociation constants Ks of glucose and maltose for the external sites, rather than the Km (zero-transoi) of glucose and the Ki of maltose. The data are also inconsistent with other forms of asymmetric carrier but are fairly consistent with a symmetrical carrier with high-affinity sites for D-glucose or with a fixed site carrier model.

摘要

模拟表明,糖转运的四态移动载体模型(其中不对称性源于游离载体和载体 - 糖复合物向内和向外转运的速率常数不相等)与A.G. 洛(A.G. Lowe)和A.R. 沃尔姆斯利(A.R. Walmsley)[1987年,《生物化学与生物物理学报》903卷,547 - 550页]最近获得的稳态前摄取的观测数据不相符。这种差异的主要原因是,稳态前通量主要由葡萄糖和麦芽糖对外侧位点的解离常数Ks决定,而非葡萄糖的Km(零转运)和麦芽糖的Ki。这些数据也与其他形式的不对称载体不一致,但与具有D - 葡萄糖高亲和力位点的对称载体或固定位点载体模型相当一致。

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