Peptic Digestion of Streptococcal M Protein II. Extraction of M Antigen from Group A Streptococci With Pepsin

Author:

Beachey Edwin H.1,Campbell Gary L.1,Ofek Itzhak1

Affiliation:

1. Veterans Administration Hospital and the Departments of Medicine and Microbiology, University of Tennessee, Memphis, Tennessee 38104

Abstract

M protein of group A streptococci was extracted by mild peptic digestion. Optimal amounts of type-specific M protein were released after 20 min of digestion with 0.02 mg of pepsin per ml at pH 5.8. Immunological analysis revealed that, unlike conventional HCl extracts, pepsin extracts lacked the surface C carbohydrate antigen and contained less non-type-specific, heat-stable cellular antigens; they also lacked detectable heat-labile T protein. Similar to HCl extracts, however, the pepsin-extracted M protein precipitated homologous-type M antisera and inhibited type-specific opsonization of homologous group A streptococci. Furthermore, the pepsin extract was capable of inducing type-specific opsonic M antibody in rabbits. This method may provide a useful initial step in the purification of M protein by reducing contaminating antigens.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference21 articles.

1. Delayed hypersensitivity to purified streptococcal M protein in guinea pigs and in man;Beachey E. H.;J. Immunol.,1969

2. Type-specific inhibition of preopsonization versus immunoprecipitation by streptococcal M proteins;Beachey E. H.;Infect. Immunity,1973

3. Studies of antibodies to non-type-specific antigens associated with streptococcal M protein in the sera of patients with rheumatic fever;Beachey E. H.;J. Immunol.,1973

4. Toxic effects of streptococcal Mi protein on platelets and polymorphonuclear leukocytes in human blood;Beachey E. H.;J. Exp. Med.,1971

5. Mediation of cytotoxic effects of streptococcal M protein by nontype-specific antibody in human sera;Beachey E. H.;J. Clin. Invest.,1973

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3