Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/100145
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Type: Journal article
Title: Discovery of novel pneumococcal surface antigen A (PsaA) inhibitors using a fragment-based drug design approach
Author: Bajaj, M.
Mamidyala, S.
Zuegg, J.
Begg, S.
Ween, M.
Luo, Z.
Huang, J.
McEwan, A.
Kobe, B.
Paton, J.
McDevitt, C.
Cooper, M.
Citation: ACS Chemical Biology, 2015; 10(6):1511-1520
Publisher: American Chemical Society
Issue Date: 2015
ISSN: 1554-8929
1554-8937
Statement of
Responsibility: 
Megha Bajaj, Sreeman K. Mamidyala, Johannes Zuegg, Stephanie L. Begg, Miranda P. Ween, Zhenyao Luo, Johnny X. Huang, Alastair G. McEwan, Bostjan Kobe, James C. Paton, Christopher A. McDevitt, and Matthew A. Cooper
Abstract: Streptococcus pneumoniae is a leading cause of life-threatening bacterial infections, especially in young children in developing countries. Pneumococcal infections can be treated with β-lactam antibiotics, but rapid emergence of multidrug-resistant strains of S. pneumoniae over the past two decades has emphasized the need to identify novel drug targets. Pneumococcal surface antigen A (PsaA) is one such target, found on the cell surface of S. pneumoniae. It functions as a high-affinity substrate-binding protein, facilitating acquisition of Mn²⁺, which has an important role in protecting S. pneumoniae from reactive oxygen species and, hence, oxidative stress. Consequently, PsaA is essential for bacterial survival and an important virulence factor, which makes it a promising target for antibiotic drug development. To design novel PsaA inhibitors, we used a combination of de novo fragment-based drug discovery and in silico virtual screening methods. We profiled a collection of low molecular weight compounds that were selected based on their structural diversity and ability to bind to apo-PsaA in a virtual docking experiment. The screening resulted in two initial hits that were further optimized by structural variation to improve their potency while maintaining their ligand efficiency and favorable physicochemical properties. The optimized hits were validated using a cell-based assay and molecular dynamics simulations. We found that virtual screening substantially augmented fragment-based drug design approaches, leading to the identification of novel pneumococcal PsaA inhibitors.
Keywords: PsaA inhibitors
Rights: © 2015 American Chemical Society
RMID: 0030025321
DOI: 10.1021/cb501032x
Grant ID: http://purl.org/au-research/grants/arc/DP120103957
http://purl.org/au-research/grants/nhmrc/1022240
http://purl.org/au-research/grants/nhmrc/565526
http://purl.org/au-research/grants/nhmrc/1071659
Appears in Collections:Molecular and Biomedical Science publications

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