Cohen L K, Kaplan S
J Biol Chem. 1981 Jun 10;256(11):5901-8.
A nonspecific solubilization of the intracytoplasmic membrane proteins from Rhodopseudomonas sphaeroides has been achieved in the absence of detergents. Following removal of the photopigments and phospholipids by acetone/methanol extractions, the protein is quantitatively solubilized in 6 M guanidine thiocyanate which is subsequently exchanged by dialysis for 7 M urea. A urea-soluble protein fraction is obtained which represents 80% of the initial protein and qualitatively contains all the polypeptides of the membrane resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis with the exception of the reaction center polypeptides M and L, and the 35.2-kilodalton species. Fractionation of the urea-soluble polypeptides on a Sepharose CL-6B column resolves into separate fractions the two major low molecular weight polypeptides identified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Further examination of these fractions by isoelectric focusing and electrophoresis at pH 4.5 in the presence of 8 M urea reveals the presence of three major species each of which has been purified to homogeneity by a combination of ion exchange chromatography and preparative electrophoretic techniques. It is believed that these three major polypeptides are components of the light-harvesting pigment-protein complexes.
在没有去污剂的情况下,已经实现了对球形红假单胞菌胞内膜蛋白的非特异性增溶。通过丙酮/甲醇萃取去除光合色素和磷脂后,蛋白质在6M硫氰酸胍中定量增溶,随后通过透析将其换成7M尿素。得到了一种尿素可溶的蛋白质组分,它占初始蛋白质的80%,并且除了反应中心多肽M和L以及35.2千道尔顿的蛋白外,定性地包含了通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分离的膜的所有多肽。在琼脂糖CL-6B柱上对尿素可溶多肽进行分级分离,将通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳鉴定的两种主要低分子量多肽分离成不同的级分。通过等电聚焦和在8M尿素存在下于pH 4.5进行电泳对这些级分进行进一步检测,发现存在三种主要蛋白,每种蛋白都通过离子交换色谱和制备电泳技术的组合纯化至均一。据信这三种主要多肽是光捕获色素-蛋白质复合物的组分。