Horger Kim S, Liu Haiyan, Rao Divya K, Shukla Suneet, Sept David, Ambudkar Suresh V, Mayer Michael
Department of Chemical Engineering, University of Michigan, 2300 Hayward Street, Ann Arbor, MI 48109, USA.
Department of Biomedical Engineering, University of Michigan, 1101 Beal Avenue, Ann Arbor, MI 48109, USA.
Biochim Biophys Acta. 2015 Feb;1848(2):643-53. doi: 10.1016/j.bbamem.2014.10.023. Epub 2014 Nov 4.
This paper describes the formation of giant proteoliposomes containing P-glycoprotein (P-gp) from a solution of small proteoliposomes that had been deposited and partially dried on a film of agarose. This preparation method generated a significant fraction of giant proteoliposomes that were free of internalized vesicles, making it possible to determine the accessible liposome volume. Measuring the intensity of the fluorescent substrate rhodamine 123 (Rho123) inside and outside these giant proteoliposomes determined the concentration of transported substrates of P-gp. Fitting a kinetic model to the fluorescence data revealed the rate of passive diffusion as well as active transport by reconstituted P-gp in the membrane. This approach determined estimates for the membrane permeability coefficient (Ps) of passive diffusion and rate constants of active transport (kT) by P-gp as a result of different experimental conditions. The Ps value for Rho123 was larger in membranes containing P-gp under all assay conditions than in membranes without P-gp indicating increased leakiness in the presence of reconstituted transmembrane proteins. For P-gp liposomes, the kT value was significantly higher in the presence of ATP than in its absence or in the presence of ATP and the competitive inhibitor verapamil. This difference in kT values verified that P-gp was functionally active after reconstitution and quantified the rate of active transport. Lastly, patch clamp experiments on giant proteoliposomes showed ion channel activity consistent with a chloride ion channel protein that co-purified with P-gp. Together, these results demonstrate several advantages of using giant rather than small proteoliposomes to characterize transport properties of transport proteins and ion channels.
本文描述了从已沉积并部分干燥在琼脂糖薄膜上的小蛋白脂质体溶液中形成含有P-糖蛋白(P-gp)的巨型蛋白脂质体的过程。这种制备方法产生了很大一部分不含内化囊泡的巨型蛋白脂质体,从而能够确定可及的脂质体体积。通过测量这些巨型蛋白脂质体内外荧光底物罗丹明123(Rho123)的强度,确定了P-gp转运底物的浓度。将动力学模型拟合到荧光数据中,揭示了被动扩散速率以及膜中重组P-gp的主动转运速率。由于不同的实验条件,这种方法确定了被动扩散的膜渗透系数(Ps)和P-gp主动转运速率常数(kT)的估计值。在所有测定条件下,含有P-gp的膜中Rho123的Ps值均大于不含P-gp的膜,这表明在存在重组跨膜蛋白的情况下泄漏增加。对于P-gp脂质体,在存在ATP时的kT值显著高于不存在ATP时或存在ATP和竞争性抑制剂维拉帕米时。kT值的这种差异证实了重组后P-gp具有功能活性,并对主动转运速率进行了量化。最后,对巨型蛋白脂质体进行的膜片钳实验显示出与与P-gp共纯化的氯离子通道蛋白一致的离子通道活性。总之,这些结果证明了使用巨型而非小蛋白脂质体来表征转运蛋白和离子通道转运特性的几个优点。