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LK绵羊红细胞膜内翻小泡中K-Cl协同转运体肿胀激活的机制。

Mechanism of swelling activation of K-Cl cotransport in inside-out vesicles of LK sheep erythrocyte membranes.

作者信息

Kelley S J, Dunham P B

机构信息

Department of Biology, Syracuse University, New York 13244, USA.

出版信息

Am J Physiol. 1996 Apr;270(4 Pt 1):C1122-30. doi: 10.1152/ajpcell.1996.270.4.C1122.

Abstract

Stimulation by swelling of K-Cl cotransport was studied in inside-out vesicles (IOVs) made from membranes of LK sheep erythrocytes. The purpose was to understand this stimulation in terms of the three-state process proposed for regulation of the cotransporter (P.B. Dunham, J. Klimczak, and P.J. Logue. J. Gen. Physiol. 101: 733-765, 1993). The first step in this process, A --> B, is rate limiting and controlled by transphosphorylation reactions. The second step, B --> C, is fast; its control is unknown. Predictions were that maximum velocity (Jmax) of cotransport increases with A --> B and concentration at one-half Jmax (K1/2) of K+ as a substrate decreases with B --> C. We tested the hypothesis that most transporters in IOVs are in the B state and that swelling activates cotransport in vesicles by the B --> C conversion. In accordance with this hypothesis, swelling should activate K+ influx with no discernable delay. It did. K1/2 for K+ should decrease with swelling and Jmax should not change. K1/2 decreased 10-fold, and Jmax did not change. Inhibitors of transphosphorylation, reactions of A --> B, should not affect K+ flux into IOVs, and they did not. The results support the hypothesis: swelling activation of K+ flux into IOVs corresponds to B --> C. A mechanical change in the membrane causes a specific change in the cotransporter: an increase in apparent affinity for K+.

摘要

在由LK绵羊红细胞膜制成的内翻囊泡(IOV)中研究了K-Cl协同转运体肿胀刺激的情况。目的是根据为协同转运体调节提出的三态过程来理解这种刺激(P.B. 邓纳姆、J. 克利姆扎克和P.J. 洛格。《普通生理学杂志》101: 733 - 765, 1993)。这个过程的第一步,A→B,是限速步骤,受转磷酸化反应控制。第二步,B→C,很快;其控制机制未知。预测是协同转运的最大速度(Jmax)随着A→B增加,而作为底物的K⁺在一半Jmax时的浓度(K1/2)随着B→C降低。我们测试了这样一个假设,即IOV中的大多数转运体处于B状态,并且肿胀通过B→C转化激活囊泡中的协同转运。根据这个假设,肿胀应该能立即激活K⁺内流。事实确实如此。K⁺的K1/2应该随着肿胀而降低,而Jmax应该不变。K1/2降低了10倍,Jmax没有变化。转磷酸化反应(A→B)的抑制剂不应影响K⁺流入IOV,实际情况也是如此。结果支持了这个假设:肿胀激活K⁺流入IOV对应于B→C。膜的机械变化导致协同转运体发生特定变化:对K⁺的表观亲和力增加。

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