Conrad M J, Penniston J T
J Biol Chem. 1976 Jan 10;251(1):253-5.
A two-dimensional electrophoresis method has been developed which solubilizes erythrocyte membrane proteins, and which resolves the components of the band that migrates in detergent gels as if its molecular mass were 95,000 daltons. This method uses gel electrophoresis with sodium dodecyl sulfate in the first dimension and phenol, aqueous urea, and acetic acid in the second dimension. The 95,000 dalton band is known to contain several different membrane proteins, including those associated with anion transport, glucose transport, and (Na+,K+) transport. Two-dimensional electrophoresis resolved this band into one major spot and several minor ones. Pronase digestion of whole erythrocytes, followed by preparation of ghosts and two-dimensional electrophoresis, showed that only the major component of this band was digested by pronase.
已开发出一种二维电泳方法,该方法可溶解红细胞膜蛋白,并能解析在去污剂凝胶中迁移的条带成分,其分子量似乎为95,000道尔顿。此方法在第一维使用十二烷基硫酸钠进行凝胶电泳,在第二维使用苯酚、尿素水溶液和乙酸。已知95,000道尔顿的条带包含几种不同的膜蛋白,包括与阴离子转运、葡萄糖转运和(Na +,K +)转运相关的蛋白。二维电泳将该条带解析为一个主要斑点和几个次要斑点。对全红细胞进行链霉蛋白酶消化,随后制备血影并进行二维电泳,结果表明该条带中只有主要成分被链霉蛋白酶消化。