Buhl A M, Sheikh M I, Steensgaard J, Røigaard-Petersen H, Jacobsen C
Institute of Medical Biochemistry, University of Aarhus, Denmark.
FEBS Lett. 1992 Jun 15;304(2-3):179-83. doi: 10.1016/0014-5793(92)80613-l.
The GTP-binding proteins on luminal and basolateral membrane vesicles from outer cortex (pars convoluta) and outer medulla (pars recta) of rabbit proximal tubule have been examined. The membrane vesicles were highly purified, as ascertained by electron microscopy, by measurements of marker enzymes, and by investigating segmental-specific transport systems. The [35S]GTP gamma S binding to vesicles, and to sodium cholate-extracted proteins from vesicles, indicated that the total content of GTP-binding proteins were equally distributed on pars convoluta, pars recta luminal and basolateral membranes. The membranes were ADP-ribosylated with [32P]NAD+ in the presence of pertussis toxin and cholera toxin. Gel electrophoresis revealed, for all preparations, the presence of cholera toxin [32P]ADP-ribosylated 42 and 45 kDa G alpha s proteins, and pertussis toxin [32P]ADP-ribosylated 41 kDa G alpha i1, 40 kDa G alpha i2 and 41 kDa G alpha i3 proteins. The 2D electrophoresis indicated that Go's were not present in luminal nor in basolateral membranes of pars convoluta or pars recta of rabbit proximal tubule.
对兔近端小管外皮质(曲部)和外髓质(直部)腔面膜囊泡和基底外侧膜囊泡上的GTP结合蛋白进行了研究。通过电子显微镜、标记酶测量以及对节段特异性转运系统的研究确定,膜囊泡已高度纯化。[35S]GTPγS与囊泡以及囊泡中经胆酸钠提取的蛋白质的结合表明,GTP结合蛋白的总含量在曲部、直部腔面和基底外侧膜上均匀分布。在百日咳毒素和霍乱毒素存在的情况下,膜用[32P]NAD+进行ADP核糖基化。凝胶电泳显示,对于所有制剂,均存在霍乱毒素[32P]ADP核糖基化的42 kDa和45 kDa Gαs蛋白,以及百日咳毒素[32P]ADP核糖基化的41 kDa Gαi1、40 kDa Gαi2和41 kDa Gαi3蛋白。二维电泳表明,兔近端小管曲部或直部的腔面或基底外侧膜中不存在Go。