THE STRUCTURAL BIOLOGY OF MOLECULAR RECOGNITION BY VANCOMYCIN
Loll, Patrick J.; Axelsen, Paul H.; Loll, Patrick J.; Departments of Pharmacology* and Medicine†, Infectious Disease Section, The Johnson Foundation for Molecular Biophysics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6084; e-mail: loll@pharm.med.upenn.edu , axe@pharm.med.upenn.edu
Журнал:
Annual Review of Biophysics and Biomolecular Structure
Дата:
2000
Аннотация:
▪ Abstract Vancomycin is the archetype among naturally occurring compounds known as glycopeptide antibiotics. Because it is a vital therapeutic agent used worldwide for the treatment of infections with gram-positive bacteria, emerging bacterial resistance to vancomycin is a major public health threat. Recent investigations into the mechanisms of action of glycopeptide antibiotics are driven by a need to understand their detailed mechanism of action so that new agents can be developed to overcome resistance. These investigations have revealed that glycopeptide antibiotics exhibit a rich array of complex cooperative phenomena when they bind target ligands, making them valuable model systems for the study of molecular recognition.
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