Transcript Slide 1

Article Title
Structural basis for the beta lactam resistance of PBP2a from methicillin-resistant Staphylococcus aureus.
Abstract
The multiple antibiotic resistance of methicillin-resistant strains of Staphylococcus aureus (MRSA) has become a major clinical problem worldwide.
The key determinant of the broad-spectrum beta-lactam resistance in MRSA strains is the penicillin-binding protein 2a (PBP2a). Because of its low
affinity for beta-lactams, PBP2a provides transpeptidase activity to allow cell wall synthesis at beta-lactam concentrations that inhibit the betalactam-sensitive PBPs normally produced by S. aureus. The crystal structure of a soluble derivative of PBP2a has been determined to 1.8 A
resolution and provides the highest resolution structure for a high molecular mass PBP. Additionally, structures of the acyl-PBP complexes of
PBP2a with nitrocefin, penicillin G and methicillin allow, for the first time, a comparison of an apo and acylated resistant PBP. An analysis of the
PBP2a active site in these forms reveals the structural basis of its resistance and identifies features in newly developed beta-lactams that are likely
important for high affinity binding.
Keywords
Acylation, Anti-Bacterial Agents, Bacterial Proteins, Binding Sites, Carrier Proteins, Drug Design, Hexosyltransferases, Lactams,
Muramoylpentapeptide Carboxypeptidase, Peptidyltransferase, Protein Conformation, Protein Structure, Tertiary, Staphylococcus, StructureActivity Relationship, Support, Non-U.S. Gov't, beta-Lactam Resistance
Authors
Lim, D., Strynadka, N.C.
Organizational Affiliation
2146 Health Sciences Mall, Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia V6T
1Z3, Canada.
Journal
Nat.Struct.Biol. v9 pp. 870-6, 2002
Pubmed ID
12389036
PDB.ORG
H.M. Berman, J. Westbrook, Z. Feng, G. Gilliland, T.N. Bhat, H. Weissig, I.N. Shindyalov, P.E. Bourne: The Protein Data Bank. Nucleic Acids
Research, 28 pp. 235-242 (2000).
ProteinScope
ProteinScope ™ & (c) Mark S. Morris 2007.
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