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Updated: Sep 5, 2026

Immuno-fluorescence Assay of Leptospiral Surface-exposed Proteins
Published on: July 1, 2011
STREPTOCOCCAL M ANTIGEN LOCATION AND SYNTHESIS, STUDIED BY IMMUNOFLUORESCENCE
Abstract:
Streptococcal M protein has been studied directly in the intact streptococcal cell by specific immunofluorescence. By this method, it can be seen to be concentrated in or on the cell wall, but cannot be detected in the capsule. The lack of type-specific (but not group-specific) immunofluorescence after trypsinization; and the inhibition of group-specific immunofluorescence by unlabeled type-specific antibody, are observations most compatible with a location of the M antigen determinants on the cell surface superficial to the group antigen. M antigen is not "resynthesized" after trypsinization of living cells, but appears anew only at sites of new cell wall growth. A limited amount of such growth, leading sometimes to detectable amounts of M in the gross, can take place in deficient media without detectable increases in optical density of the cell population.
Insights
Streptococcal M protein is located on the cell wall surface, not in the capsule. It appears at new cell wall growth sites after trypsinization, indicating its superficial location.
Area of Science:
- Microbiology
- Immunology
- Cell Biology
Background:
- Streptococcal M protein is a key virulence factor.
- Its precise location on the bacterial cell surface is crucial for understanding host-pathogen interactions.
Purpose of the Study:
- To determine the exact location of Streptococcal M protein on the intact bacterial cell.
- To investigate the relationship between M protein, group antigen, and cell wall structure.
Main Methods:
- Specific immunofluorescence was used to visualize M protein on intact streptococcal cells.
- Trypsinization was employed to assess the protein's accessibility and resynthesis.
- Immunofluorescence inhibition assays were performed using specific antibodies.
Main Results:
- M protein was found concentrated in or on the cell wall, but not within the capsule.
- Type-specific M protein immunofluorescence was lost after trypsinization, while group-specific fluorescence remained.
- M protein was not resynthesized after trypsinization but reappeared at sites of new cell wall growth.
Conclusions:
- Streptococcal M protein determinants are located superficially on the cell surface, external to the group antigen.
- M protein localization is linked to new cell wall synthesis, not continuous resynthesis.
- These findings clarify the spatial organization of M protein and its implications for streptococcal virulence.
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