Structural basis of Mycobacterium tuberculosis transcription and transcription inhibition

Lin, W.; Mandal, S.; Degen, D.; Liu, Y.; Ebright, Y.; Li, S.; Feng, Y.; Zhang, Y.; Jiang, Y.; Liu, S.; Gigliotti, M.; Talaue, M.; Connell, N.; Das, K.; Arnold, E.; Ebright, R. H.

doi:10.1101/099606

bioRxiv · 10.1101/099606

Structural basis of Mycobacterium tuberculosis transcription and transcription inhibition

Lin, W.·Mandal, S.·Degen, D.·Liu, Y.·Ebright, Y.·Li, S.·Feng, Y.·Zhang, Y.·Jiang, Y.·Liu, S.·Gigliotti, M.·Talaue, M.·Connell, N.·Das, K.·Arnold, E.·Ebright, R. H.

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Abstract

One Sentence SummaryStructures of Mycobacterium tuberculosis RNA polymerase reveal taxon-specific properties and binding sites of known and new antituberculosis agents\n\nAbstractMycobacterium tuberculosis (Mtb) is the causative agent of tuberculosis, which kills 1.8 million annually. Mtb RNA polymerase (RNAP) is the target of the first-line antituberculosis drug rifampin (Rif). We report crystal structures of Mtb RNAP, alone and in complex with Rif. The results identify an Mtb-specific structural module of Mtb RNAP and establish that Rif functions by a steric-occlusion mechanism that prevents extension of RNA. We also report novel non-Rif-related compounds-N-aroyl-N-aryl-phenylalaninamides (AAPs)-that potently and selectively inhibit Mtb RNAP and Mtb growth, and we report crystal structures of Mtb RNAP in complex with AAPs. AAPs bind to a different site on Mtb RNAP than Rif, exhibit no cross-resistance with Rif, function additively when co-administered with Rif, and suppress resistance emergence when co-administered with Rif.

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Lin, W., Mandal, S., Degen, D., Liu, Y., Ebright, Y., Li, S., Feng, Y., Zhang, Y., Jiang, Y., Liu, S., Gigliotti, M., Talaue, M., Connell, N., Das, K., Arnold, E., Ebright, R. H.. 2017-01-10. Structural basis of Mycobacterium tuberculosis transcription and transcription inhibition. https://doi.org/10.1101/099606

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