Russell H, Facklam R R
Infect Immun. 1975 Sep;12(3):679-86. doi: 10.1128/iai.12.3.679-686.1975.
A new method of extracting M protein from streptococcal cell walls has been presented. The extracting agent was guanidine-hydrochloride, a protein denaturant. The crude guanidine extract was further purified by ammonium sulfate and pH 5 fractionation and by hydroxyapatite column chromatography. Three major protein peaks were eluted from the hydroxyapatite column with 0.01, 0.1 and 0.3 M phosphate buffer, respectively. Protein fractions eluted at 0.1 and 0.3 M phosphate concentractions contained antigens that precipitated with homologous M-protein specific antisera, whereas the 0.01 M phosphate fraction had no immunological activity. The fraction eluted with 0.3 M phosphate was electrophoretically homogeneous in sodium dodecyl sulfate-acrylamide gels and elicited the production of bactericidal antibodies in rabbits. The 0.1 M phosphate buffer eluant was electrophoretically heterogeneous and did not elicit the production of bactericidal antibodies in rabbits.
一种从链球菌细胞壁中提取M蛋白的新方法已被提出。提取剂是盐酸胍,一种蛋白质变性剂。粗制的胍提取物通过硫酸铵和pH 5分级分离以及羟基磷灰石柱色谱进一步纯化。分别用0.01、0.1和0.3 M磷酸盐缓冲液从羟基磷灰石柱上洗脱下来三个主要的蛋白质峰。在0.1和0.3 M磷酸盐浓度下洗脱的蛋白质组分含有能与同源M蛋白特异性抗血清沉淀的抗原,而0.01 M磷酸盐组分没有免疫活性。用0.3 M磷酸盐洗脱的组分在十二烷基硫酸钠-丙烯酰胺凝胶中电泳均一,并且能在兔体内引发杀菌抗体的产生。用0.1 M磷酸盐缓冲液洗脱的组分电泳不均一,并且不能在兔体内引发杀菌抗体的产生。