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A mass spectrometry-based assay for improved quantitative measurements of efflux pump inhibition.
Brown, Adam R; Ettefagh, Keivan A; Todd, Daniel; Cole, Patrick S; Egan, Joseph M; Foil, Daniel H; Graf, Tyler N; Schindler, Bryan D; Kaatz, Glenn W; Cech, Nadja B.
Afiliação
  • Brown AR; Department of Chemistry/Biochemistry, The University of North Carolina Greensboro, Greensboro, North Carolina, United States of America.
  • Ettefagh KA; Department of Chemistry/Biochemistry, The University of North Carolina Greensboro, Greensboro, North Carolina, United States of America.
  • Todd D; Department of Chemistry/Biochemistry, The University of North Carolina Greensboro, Greensboro, North Carolina, United States of America.
  • Cole PS; Department of Chemistry/Biochemistry, The University of North Carolina Greensboro, Greensboro, North Carolina, United States of America.
  • Egan JM; Department of Chemistry/Biochemistry, The University of North Carolina Greensboro, Greensboro, North Carolina, United States of America.
  • Foil DH; Department of Chemistry/Biochemistry, The University of North Carolina Greensboro, Greensboro, North Carolina, United States of America.
  • Graf TN; Department of Chemistry/Biochemistry, The University of North Carolina Greensboro, Greensboro, North Carolina, United States of America.
  • Schindler BD; Division of Infectious Disease, John Dingell Department of Veteran Affairs Medical Center and Department of Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan, United States of America.
  • Kaatz GW; Division of Infectious Disease, John Dingell Department of Veteran Affairs Medical Center and Department of Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan, United States of America.
  • Cech NB; Department of Chemistry/Biochemistry, The University of North Carolina Greensboro, Greensboro, North Carolina, United States of America.
PLoS One ; 10(5): e0124814, 2015.
Article em En | MEDLINE | ID: mdl-25961825
ABSTRACT
Bacterial efflux pumps are active transport proteins responsible for resistance to selected biocides and antibiotics. It has been shown that production of efflux pumps is up-regulated in a number of highly pathogenic bacteria, including methicillin resistant Staphylococcus aureus. Thus, the identification of new bacterial efflux pump inhibitors is a topic of great interest. Existing assays to evaluate efflux pump inhibitory activity rely on fluorescence by an efflux pump substrate. When employing these assays to evaluate efflux pump inhibitory activity of plant extracts and some purified compounds, we observed severe optical interference that gave rise to false negative results. To circumvent this problem, a new mass spectrometry-based method was developed for the quantitative measurement of bacterial efflux pump inhibition. The assay was employed to evaluate efflux pump inhibitory activity of a crude extract of the botanical Hydrastis Canadensis, and to compare the efflux pump inhibitory activity of several pure flavonoids. The flavonoid quercetin, which appeared to be completely inactive with a fluorescence-based method, showed an IC50 value of 75 µg/mL with the new method. The other flavonoids evaluated (apigenin, kaempferol, rhamnetin, luteolin, myricetin), were also active, with IC50 values ranging from 19 µg/mL to 75 µg/mL. The assay described herein could be useful in future screening efforts to identify efflux pump inhibitors, particularly in situations where optical interference precludes the application of methods that rely on fluorescence.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espectrometria de Massas / Transporte Biológico / Proteínas de Transporte Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espectrometria de Massas / Transporte Biológico / Proteínas de Transporte Idioma: En Ano de publicação: 2015 Tipo de documento: Article