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- W4243948319 endingPage "188" @default.
- W4243948319 startingPage "173" @default.
- W4243948319 abstract "Prior to bacterial genome sequencing and the genetic analysis of pathogenesis, microbiologists identified molecules on microbial surfaces and studied their role in disease processes (1). The ultimate goal of this research was the identification of molecular formulations inciting antibody responses in vaccine recipients that prevented disease yet would otherwise not cause harm (2). Oswald Avery's discovery of the pneumococcus capsule and the demonstration that capsular polysaccharide vaccine protects against pneumococcal pneumonia represent an important paradigm (3, 4). Another was Rebecca Lancefield's characterization of M protein as the determinant of type-specific immunity against Streptococcus pyogenes, the causative agent of streptococcal pharyngitis and rheumatic fever (2). Lancefield and Sjöquist required proteases or peptidoglycan (murein) hydrolases, but not membrane detergents, to solubilize surface proteins of Gram-positive bacteria (2, 5, 6). The underlying reason for this biochemical phenomenon is that surface proteins are covalently linked to peptidoglycan at their C-terminal ends (7, 8)." @default.
- W4243948319 created "2022-05-12" @default.
- W4243948319 creator A5005368537 @default.
- W4243948319 creator A5083683183 @default.
- W4243948319 date "2019-09-12" @default.
- W4243948319 modified "2023-09-25" @default.
- W4243948319 title "Sortases, Surface Proteins, and Their Roles in<i>Staphylococcus aureus</i>Disease and Vaccine Development" @default.
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