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Studying antibiotic-membrane interactions via X-ray diffraction and fluorescence microscopy.

ABSTRACT: Antibiotic drug resistance is a serious issue for the treatment of bacterial infection. Understanding the resistance to antibiotics is a key issue for developing new drugs. We used penicillin and sulbactam as model antibiotics to study their interaction with model membranes. Cholesterol was used to target the membrane for comparison with the well-known insertion model. Lamellar X-ray diffraction (LXD) was used to determine membrane thickness using successive drug-to-lipid molar ratios. The aspiration method for a single giant unilamellar vesicle (GUV) was used to monitor the kinetic binding process of antibiotic-membrane interactions in an aqueous solution. Both penicillin and sulbactam are found positioned outside the model membrane, while cholesterol inserts perpendicularly into the hydrophobic region of the membrane in aqueous solution. This result provides structural insights for understanding the antibiotic-membrane interaction and the mechanism of antibiotics.

SUBMITTER: Sun YT

PROVIDER: S-EPMC4491592 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Studying antibiotic-membrane interactions via X-ray diffraction and fluorescence microscopy.

Sun Yi-Ting YT Huang Ping-Yuan PY Lin Cheng-Hao CH Lee Kuan-Rong KR Lee Ming-Tao MT

FEBS open bio 20150615

Antibiotic drug resistance is a serious issue for the treatment of bacterial infection. Understanding the resistance to antibiotics is a key issue for developing new drugs. We used penicillin and sulbactam as model antibiotics to study their interaction with model membranes. Cholesterol was used to target the membrane for comparison with the well-known insertion model. Lamellar X-ray diffraction (LXD) was used to determine membrane thickness using successive drug-to-lipid molar ratios. The aspir ...[more]

PMID: 26155459

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