RT Journal Article
SR Electronic
T1 Pyrazinamide triggers degradation of its target aspartate decarboxylase
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 674416
DO 10.1101/674416
A1 Pooja Gopal
A1 Jickky Sarathy
A1 Michelle Yee
A1 Priya Ragunathan
A1 Joon Shin
A1 Shashi Bhushan
A1 Junhao Zhu
A1 Tatos Akopian
A1 Olga Kandror
A1 Teck Kwang Lim
A1 Martin Gengenbacher
A1 Qingsong Lin
A1 Eric J. Rubin
A1 Gerhard Grüber
A1 Thomas Dick
YR 2019
UL http://biorxiv.org/content/early/2019/06/18/674416.abstract
AB The introduction of pyrazinamide (PZA) in the tuberculosis drug regimen shortened treatment from 12 to 6 months 1. PZA is a prodrug that is activated by a Mycobacterium tuberculosis (Mtb) amidase to release its bioactive component pyrazinoic acid (POA) 2. Aspartate decarboxylase PanD, a proenzyme activated by autocatalytic cleavage (Supplementary Fig. 1A, 3) and required for Coenzyme A (CoA) biosynthesis, emerged as a target of POA 4-7. In vitro and in vivo screening to isolate spontaneous POA-resistant Mtb mutants identified missense mutations in either panD or the unfoldase clpC1, encoding a component of the caseinolytic protease ClpC1-ClpP 4,6-9. Overexpression and binding studies of PanD or ClpC1 pointed to PanD as the direct target of POA whereas clpC1 mutations appeared to indirectly cause resistance 4,5,7,9,10. Indeed, supplementing growth media with CoA precursors downstream of the PanD catalyzed step conferred POA resistance 4,7,11. Metabolomic analyses and biophysical studies using recombinant proteins confirmed targeting of PanD by POA 5. However, the exact molecular mechanism of PanD inhibition by POA remained unknown. While most drugs act by inhibiting protein function upon target binding, we show here that POA is not a bona fide enzyme inhibitor. Rather, POA binding to PanD triggers degradation of the protein by ClpC1-ClpP. Thus, the old tuberculosis drug PZA promotes degradation of its target. While novel for an antibacterial, drug-induced target degradation has recently emerged as a strategy in drug discovery across disease indications. Our findings provide the basis for the rational discovery of next generation PZA.