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The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route

Embryonic hematopoiesis

© Giulia Manina, Institut Pasteur

Mycobacterium tuberculosis dual fluorescent reporter of metabolic activity. Green (active bacilli) and red fluorescence (quiescent bacilli) are merged, 100X magnification.

Publication : Applied microbiology and biotechnology

The DprE1 enzyme, one of the most vulnerable targets of Mycobacterium tuberculosis

Team: Microbial Individuality and Infection

Member: Giulia Manina

Scientific Fields

Diseases

Organisms

Applications

Technique

Published in Applied microbiology and biotechnology - 14 Sep 2013

Riccardi G, Pasca MR, Chiarelli LR, Manina G, Mattevi A, Binda C

Link to Pubmed [PMID] – 24037308

Appl. Microbiol. Biotechnol. 2013 Oct;97(20):8841-8

The re-emergence of tuberculosis in recent years led the World Health Organization (WHO) to launch the Stop TB Strategy program. Beside repurposing the existing drugs and exploring novel molecular combinations, an essential step to face the burden of tuberculosis will be to develop new drugs by identifying vulnerable bacterial targets. Recent studies have focused on decaprenylphosphoryl-D-ribose oxidase (DprE1) of Mycobacterium tuberculosis, an essential enzyme involved in cell wall metabolism, for which new promising molecules have proved efficacy as antitubercular agents. This review summarizes the state of the art concerning DprE1 in terms of structure, enzymatic activity and inhibitors. This enzyme is emerging as one of the most vulnerable target in M. tuberculosis.

Published on: 14 Sep 2013