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使用Cl(-)敏感荧光探针表征液泡膜囊泡中的Cl-转运:Cl-通量电压和浓度依赖性的反应动力学模型

Characterization of Cl- transport in vacuolar membrane vesicles using a Cl(-)-sensitive fluorescent probe: reaction kinetic models for voltage- and concentration-dependence of Cl- flux.

作者信息

Pope A J, Jennings I R, Sanders D, Leigh R A

机构信息

AFRC Institute of Arable Crops Research, Rothamsted Experimental Station, Harpenden, Hertfordshire, United Kingdom.

出版信息

J Membr Biol. 1990 Jun;116(2):129-37. doi: 10.1007/BF01868671.

Abstract

The effects of Cl- concentration and membrane potential (delta psi) on Cl- influx in isolated vesicles of vacuolar membrane (tonoplast) from red beet (Beta vulgaris L.) storage tissue have been characterized using the Cl(-)-sensitive fluorescent probe, 6-methoxy-1-(3-sulfonatopropyl)quinolinium (SPQ). The initial rate of Cl- transport into the vesicles was enhanced both by the imposition of a positive delta psi and by increases in extravesicular Cl- concentration. The kinetic mechanism underlying these responses was investigated by examining the accuracy with which the data could be described by several transport models. A model based on constant field theory yielded a poor description of the data, but satisfactory fits were generated by pseudo-two-state reaction kinetic models based on classical carrier schemes. Fits were equally good when it was assumed that charge translocation accompanied Cl- entry, or when charge was carried by the unloaded transport system, as long as only a single charge is translocated in each carrier cycle. Expansion of the models to three states enabled description of the Cl- concentration dependence of transport by changes in a single, voltage insensitive rate constant which is tentatively identified with Cl- binding at the external surface of the membrane. The derived value of the dissociation constant between Cl- and the transport system is estimated at between 30 and 52 mM.

摘要

利用对Cl⁻敏感的荧光探针6-甲氧基-1-(3-磺丙基)喹啉鎓(SPQ),对来自红甜菜(Beta vulgaris L.)贮藏组织的液泡膜(液泡质膜)分离囊泡中Cl⁻浓度和膜电位(Δψ)对Cl⁻内流的影响进行了表征。通过施加正的Δψ和增加囊泡外Cl⁻浓度,均可提高Cl⁻转运到囊泡中的初始速率。通过研究几种转运模型对数据的拟合精度,探究了这些响应背后的动力学机制。基于恒定场理论的模型对数据的描述较差,但基于经典载体机制的伪二态反应动力学模型能产生令人满意的拟合。当假设电荷转运伴随Cl⁻进入时,或者当电荷由空载转运系统携带时,拟合效果同样良好,只要在每个载体循环中只有一个电荷发生转运。将模型扩展到三态能够通过一个单一的、对电压不敏感的速率常数的变化来描述Cl⁻转运的浓度依赖性,该速率常数初步确定为膜外表面的Cl⁻结合。Cl⁻与转运系统之间的解离常数估计值在30至52 mM之间。

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