| Literature DB >> 29140595 |
Anfal Motib1, Antonio Guerreiro2, Firas Al-Bayati1, Elena Piletska3, Irfan Manzoor4, Sulman Shafeeq4, Anagha Kadam5, Oscar Kuipers4, Luisa Hiller5, Todd Cowen3, Sergey Piletsky3, Peter W Andrew1, Hasan Yesilkaya1.
Abstract
We describe the development, characterization, and biological testing of a new type of linear molecularly imprinted polymer (LMIP) designed to act as an anti-infective by blocking the quorum sensing (QS) mechanism and so abrogating the virulence of the pathogen Streptococcus pneumoniae. The LMIP is prepared (polymerized) in presence of a template molecule, but unlike in traditional molecular imprinting approaches, no cross-linker is used. This results in soluble low-molecular-weight oligomers that can act as a therapeutic agent in vitro and in vivo. The LMIP was characterized by mass spectrometry to determine its monomer composition. Fragments identified were then aligned along the peptide template by computer modeling to predict the possible monomer sequence of the LMIP. These findings provide a proof of principle that LMIPs can be used to block QS, thus setting the stage for the development of LMIPs a novel drug-discovery platform and class of materials to target Gram-positive pathogens.Entities:
Keywords: antibacterial agents; molecular imprinting; quorum sensing; receptors; virulence factors
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Year: 2017 PMID: 29140595 DOI: 10.1002/anie.201709313
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336