Literature DB >> 24391095

Penicillin-binding protein imaging probes.

Ozden Kocaoglu1, Erin E Carlson.   

Abstract

Penicillin-binding proteins (PBPs) are membrane-associated proteins involved in the biosynthesis of peptidoglycan (PG), the main component of bacterial cell walls. These proteins were discovered and named for their affinity to bind the β-lactam antibiotic penicillin. The importance of the PBPs has long been appreciated; however, the apparent functional redundancy of the ~5 to 15 proteins that most bacteria possess makes determination of their individual roles difficult. Existing techniques to study PBPs are not ideal because they do not directly visualize protein activity and can suffer from artifacts. Therefore, development of new methods for studying the roles of distinct PBPs in cell wall synthesis was compulsory. Due to penicillin's covalent mode of inhibition, fluorophore-conjugated analogs can be utilized to visualize PBP activity. Herein, we describe a general protocol to label and detect subsets of active PBPs in live, Gram-positive bacteria using fluorescent β-lactams.

Entities:  

Keywords:  activity-based probes; fluorescence imaging; penicillin-binding proteins; peptidoglycan; β-lactams

Mesh:

Substances:

Year:  2013        PMID: 24391095      PMCID: PMC3918497          DOI: 10.1002/9780470559277.ch130102

Source DB:  PubMed          Journal:  Curr Protoc Chem Biol        ISSN: 2160-4762


  14 in total

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Review 5.  Peptidoglycan structure and architecture.

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7.  Selective penicillin-binding protein imaging probes reveal substructure in bacterial cell division.

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  10 in total

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Review 6.  Progress and prospects for small-molecule probes of bacterial imaging.

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10.  Stationary phase persister formation in Escherichia coli can be suppressed by piperacillin and PBP3 inhibition.

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