Edwards J J, Anderson N G, Nance S L, Anderson N L
Blood. 1979 Jun;53(6):1121-32.
Human erythrocyte lysate proteins were resolved into over 250 discrete spots by two-dimensional electrophoresis using isoelectric focusing in the first dimension and electrophoresis in the presence of sodium dodecyl sulfate, (SDS) in the second. The overwhelming excess of hemoglobin has made such analyses difficult in the past. However, with the ISO-DALT two-dimensional electrophoresis system, large numbers of red cell proteins can be mapped in the presence of hemoglobin. When hemoglobin and several other major proteins are removed by adsorption to DEAE-cellulose, additional minor components are seen, giving a total of over 275. With the use of purified preparations, the map positions of five cell enzymes or their subunits were determined: pyruvate kinase, catalase, glucose-6-phosphate dehydrogenase, hypoxanthine phosphoribosyltransferase, and carbonic anhydrase. The mapping techniques described complement and extend those traditionally used to find human red cell protein variants.
通过二维电泳,利用等电聚焦作为第一维,在十二烷基硫酸钠(SDS)存在的情况下进行第二维电泳,人类红细胞裂解物蛋白质可分离成250多个离散的斑点。过去,由于血红蛋白的大量存在,此类分析一直很困难。然而,使用ISO-DALT二维电泳系统,可以在血红蛋白存在的情况下对大量红细胞蛋白质进行图谱分析。当血红蛋白和其他几种主要蛋白质通过吸附到DEAE-纤维素上被去除后,可以看到更多的次要成分,总数超过275种。通过使用纯化制剂,确定了五种细胞酶或其亚基的图谱位置:丙酮酸激酶、过氧化氢酶、葡萄糖-6-磷酸脱氢酶、次黄嘌呤磷酸核糖转移酶和碳酸酐酶。所描述的图谱技术补充并扩展了传统上用于发现人类红细胞蛋白质变体的技术。