4 research outputs found
Additional file 2 of Mediation analysis of erythrocyte lipophilic index on the association between BMI and risk of oral cancer
Additional file 2: Supplement Table 1. Multivariable generalized Linear Models of mediation of outcome models
Development of Oxadiazolone Activity-Based Probes Targeting FphE for Specific Detection of Staphylococcus aureus Infections
Staphylococcus aureus (S. aureus) is a major human pathogen that is responsible
for a wide range of systemic infections. Since its propensity to form
biofilms in vivo poses formidable challenges for
both detection and treatment, tools that can be used to specifically
image S. aureus biofilms are highly
valuable for clinical management. Here, we describe the development
of oxadiazolone-based activity-based probes to target the S. aureus-specific serine hydrolase FphE. Because
this enzyme lacks homologues in other bacteria, it is an ideal target
for selective imaging of S. aureus infections.
Using X-ray crystallography, direct cell labeling, and mouse models
of infection, we demonstrate that oxadiazolone-based probes enable
specific labeling of S. aureus bacteria
through the direct covalent modification of the FphE active site serine.
These results demonstrate the utility of the oxadizolone electrophile
for activity-based probes and validate FphE as a target for the development
of imaging contrast agents for the rapid detection of S. aureus infections
Development of Oxadiazolone Activity-Based Probes Targeting FphE for Specific Detection of Staphylococcus aureus Infections
Staphylococcus aureus (S. aureus) is a major human pathogen that is responsible
for a wide range of systemic infections. Since its propensity to form
biofilms in vivo poses formidable challenges for
both detection and treatment, tools that can be used to specifically
image S. aureus biofilms are highly
valuable for clinical management. Here, we describe the development
of oxadiazolone-based activity-based probes to target the S. aureus-specific serine hydrolase FphE. Because
this enzyme lacks homologues in other bacteria, it is an ideal target
for selective imaging of S. aureus infections.
Using X-ray crystallography, direct cell labeling, and mouse models
of infection, we demonstrate that oxadiazolone-based probes enable
specific labeling of S. aureus bacteria
through the direct covalent modification of the FphE active site serine.
These results demonstrate the utility of the oxadizolone electrophile
for activity-based probes and validate FphE as a target for the development
of imaging contrast agents for the rapid detection of S. aureus infections
Additional file 1 of Mediation analysis of erythrocyte lipophilic index on the association between BMI and risk of oral cancer
Additional file 1: Supplement Figure 1. Association between the lipophilic index and oral cancer by stratified analysis