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Published on: August 11, 2018
Subcellular localization of the Streptococcus mutans P1 protein C terminus
M K Homonylo-McGavin1, S F Lee, G H Bowden
1Department of Oral Biology, Faculty of Dentistry, University of Manitoba, Winnipeg, Canada.
Insights
The Streptococcus mutans P1 protein
Area of Science:
- Microbiology
- Molecular Biology
- Cell Biology
Background:
- Streptococcus mutans is a key pathogen in dental caries.
- The P1 protein's role and localization are crucial for understanding its function.
- Previous studies have not precisely defined the P1 protein's C-terminal anchor location.
Purpose of the Study:
- To ascertain the subcellular localization of the Streptococcus mutans P1 protein's C-terminal anchor.
- To investigate the association of the P1 protein with cell wall components, particularly peptidoglycan.
Main Methods:
- Cell envelope fractionation of Streptococcus mutans.
- Western immunoblotting using specific monoclonal (MAb 6-8C) and polyclonal (anti-P1COOH) antibodies.
- Enzymatic (mutanolysin) and chemical (trichloroacetic acid) treatments of cell wall components.
Main Results:
- Monoclonal antibody detected P1 protein in cell walls, but not membranes.
- Polyclonal antibody against P1 C-terminus (P1COOH) only recognized P1 after mutanolysin treatment of cell walls, indicating epitope masking by peptidoglycan.
- P1 protein was exclusively associated with peptidoglycan, not cell-wall-associated carbohydrates.
Conclusions:
- The C-terminal 144 amino acids of the P1 protein are embedded within the Streptococcus mutans cell wall.
- P1 protein is tightly associated with peptidoglycan, suggesting intercalation within the peptidoglycan strands.
- The localization implies a structural role for P1 protein within the bacterial cell wall.
Abstract:
To determine the subcellular location of the Streptococcus mutans P1 protein C-terminal anchor, cell envelope fractionation experiments were conducted in combination with Western immunoblotting, using monoclonal antibody MAb 6-8C specific for an epitope that maps near the C terminus of P1 protein and also a polyclonal antibody preparation directed against the P1 C-terminal 144 amino acids (P1COOH). P1 protein was detected in cell walls but not the membrane purified from S. mutans cells by the monoclonal antibody. In contrast, P1 protein was not detected in the same cell wall preparation using the anti-P1COOH polyclonal antibody. However, proteins released from the cell walls by treatment with mutanolysin contained antigen that was recognized by the anti-P1COOH antibody, suggesting that the epitopes recognized by the antibody were masked by peptidoglycan in the cell wall preparations. When cell walls were treated with boiling trichloroacetic acid to solubilize cell-wall-associated carbohydrate, P1 antigen could not be detected in either the solubilized carbohydrate, or in the remaining peptidoglycan, regardless of whether polyclonal or monoclonal antibody was used. However, when the peptidoglycan was treated with mutanolysin, P1 antigen could be detected in the mutanolysin solubilized fraction by MAb 6-8C. Collectively, these data suggest that the C-terminal 144 amino acids of the P1 protein are embedded within the cell wall, and associated exclusively with the peptidoglycan. Furthermore, the ability of the anti-P1COOH antibody to recognize P1 antigen only after mutanolysin treatment of cell walls suggests these C-terminal 144 amino acids are tightly intercalated within the peptidoglycan strands.
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