Koetters P J, Chou H F, Jonas A J
Department of Pediatrics, Harbor-UCLA Medical Center, Torrance 90502, USA.
Biochim Biophys Acta. 1995 Jun 9;1244(2-3):311-6. doi: 10.1016/0304-4165(95)00036-b.
As part of a strategy to purify the lysosomal sulfate transporter, we developed a method for reconstitution of transport in artificial membrane vesicles. Lysosomal membranes were prepared from Percoll density gradient purified rat liver lysosomes and membrane proteins were solubilized using the non-ionic detergent, Triton X-100. The solubilized proteins were mixed with liposomes prepared by sonication of egg yolk lecithin and the detergent was removed by passage of the mixture over Bio-beads XAD2. The resulting proteoliposomes exhibited saturable sulfate transport with characteristics that were very similar to those observed in lysosomal membranes. Transport in proteoliposomes had a Km of 155 microM, exhibited pH dependence and was sensitive to inhibition by DIDS. Reconstitution of transport in proteoliposomes may be useful as an assay for purification of the lysosomal sulfate carrier.
作为纯化溶酶体硫酸盐转运蛋白策略的一部分,我们开发了一种在人工膜囊泡中重建转运的方法。溶酶体膜由经Percoll密度梯度纯化的大鼠肝脏溶酶体制备,膜蛋白用非离子去污剂Triton X-100溶解。将溶解的蛋白与通过超声处理蛋黄卵磷脂制备的脂质体混合,混合物通过Bio-beads XAD2柱以去除去污剂。所得的蛋白脂质体表现出可饱和的硫酸盐转运,其特性与在溶酶体膜中观察到的非常相似。蛋白脂质体中的转运Km为155 microM,表现出pH依赖性,并且对DIDS抑制敏感。蛋白脂质体中转运的重建可能作为纯化溶酶体硫酸盐载体的一种测定方法。