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Research | 8 January 2021 | Open
Mechanism of filament formation in UPA-promoted CARD8 and NLRP1 inflammasomes
- L. Robert Hollingsworth
- , Liron David
- , Yang Li
- , Andrew R. Griswold
- , Jianbin Ruan
- , Humayun Sharif
- , Pietro Fontana
- , Elizabeth L. Orth-He
- , Tian-Min Fu
- , Daniel A. Bachovchin
- & Hao Wu
Nature Communications 12 , 1–13

Rights & permissionsfor article Mechanism of filament formation in UPA-promoted CARD8 and NLRP1 inflammasomes . Opens in a new window.
Amendments and Corrections | 18 May 2016
Erratum: Chemoproteomic profiling of host and pathogen enzymes active in cholera
- Stavroula K Hatzios
- , Sören Abel
- , Julianne Martell
- , Troy Hubbard
- , Jumpei Sasabe
- , Diana Munera
- , Lars Clark
- , Daniel A Bachovchin
- , Firdausi Qadri
- , Edward T Ryan
- , Brigid M Davis
- , Eranthie Weerapana
- & Matthew K Waldor
Nature Chemical Biology 12 , 466–466

Rights & permissionsfor article Erratum: Chemoproteomic profiling of host and pathogen enzymes active in cholera . Opens in a new window.
Amendments and Corrections | 15 February 2012
Correction: Corrigendum: Click-generated triazole ureas as ultrapotent in vivo–active serine hydrolase inhibitors
- Alexander Adibekian
- , Brent R Martin
- , Chu Wang
- , Ku-Lung Hsu
- , Daniel A Bachovchin
- , Sherry Niessen
- , Heather Hoover
- & Benjamin F Cravatt
Nature Chemical Biology 8 , 318–318

Rights & permissionsfor article Correction: Corrigendum: Click-generated triazole ureas as ultrapotent <i>in vivo</i>–active serine hydrolase inhibitors . Opens in a new window.
Amendments and Corrections | 1 May 2009
Erratum: Identification of selective inhibitors of uncharacterized enzymes by high-throughput screening with fluorescent activity-based probes
Nature Biotechnology 27 , 485–485

Rights & permissionsfor article Erratum: Identification of selective inhibitors of uncharacterized enzymes by high-throughput screening with fluorescent activity-based probes . Opens in a new window.
Research | 14 August 2020 | Open
DPP8/9 inhibitors activate the CARD8 inflammasome in resting lymphocytes
Cell Death & Disease 11 , 1–10

Rights & permissionsfor article DPP8/9 inhibitors activate the CARD8 inflammasome in resting lymphocytes . Opens in a new window.
Research | 5 August 2019 | Open
DPP8/9 inhibitors are universal activators of functional NLRP1 alleles
- Kuo Gai
- , Marian C. Okondo
- , Sahana D. Rao
- , Ashley J. Chui
- , Daniel P. Ball
- , Darren C. Johnson
- & Daniel A. Bachovchin
Cell Death & Disease 10 , 1–10

Rights & permissionsfor article DPP8/9 inhibitors are universal activators of functional NLRP1 alleles . Opens in a new window.
Research | 2 July 2018
DPP8/DPP9 inhibitor-induced pyroptosis for treatment of acute myeloid leukemia
Nature Medicine 24 , 1151–1156

Rights & permissionsfor article DPP8/DPP9 inhibitor-induced pyroptosis for treatment of acute myeloid leukemia . Opens in a new window.
Research | 7 November 2016
DPP8 and DPP9 inhibition induces pro-caspase-1-dependent monocyte and macrophage pyroptosis
- Marian C Okondo
- , Darren C Johnson
- , Ramya Sridharan
- , Eun Bin Go
- , Ashley J Chui
- , Mitchell S Wang
- , Sarah E Poplawski
- , Wengen Wu
- , Yuxin Liu
- , Jack H Lai
- , David G Sanford
- , Michael O Arciprete
- , Todd R Golub
- , William W Bachovchin
- & Daniel A Bachovchin
Nature Chemical Biology 13 , 46–53

Rights & permissionsfor article DPP8 and DPP9 inhibition induces pro-caspase-1-dependent monocyte and macrophage pyroptosis . Opens in a new window.
Research | 22 March 2017
LACTB is a tumour suppressor that modulates lipid metabolism and cell state
- Zuzana Keckesova
- , Joana Liu Donaher
- , Jasmine De Cock
- , Elizaveta Freinkman
- , Susanne Lingrell
- , Daniel A. Bachovchin
- , Brian Bierie
- , Verena Tischler
- , Aurelia Noske
- , Marian C. Okondo
- , Ferenc Reinhardt
- , Prathapan Thiru
- , Todd R. Golub
- , Jean E. Vance
- & Robert A. Weinberg
Nature 543 , 681–686

Rights & permissionsfor article LACTB is a tumour suppressor that modulates lipid metabolism and cell state . Opens in a new window.
Research | 22 February 2016
Chemoproteomic profiling of host and pathogen enzymes active in cholera
- Stavroula K Hatzios
- , Sören Abel
- , Julianne Martell
- , Troy Hubbard
- , Jumpei Sasabe
- , Diana Munera
- , Lars Clark
- , Daniel A Bachovchin
- , Firdausi Qadri
- , Edward T Ryan
- , Brigid M Davis
- , Eranthie Weerapana
- & Matthew K Waldor
Nature Chemical Biology 12 , 268–274

Rights & permissionsfor article Chemoproteomic profiling of host and pathogen enzymes active in cholera . Opens in a new window.
Research | 6 July 2014
A high-throughput, multiplexed assay for superfamily-wide profiling of enzyme activity
- Daniel A Bachovchin
- , Luke W Koblan
- , Wengen Wu
- , Yuxin Liu
- , Youhua Li
- , Peng Zhao
- , Iwona Woznica
- , Ying Shu
- , Jack H Lai
- , Sarah E Poplawski
- , Christopher P Kiritsy
- , Sarah E Healey
- , Matthew DiMare
- , David G Sanford
- , Robert S Munford
- , William W Bachovchin
- & Todd R Golub
Nature Chemical Biology 10 , 656–663

Rights & permissionsfor article A high-throughput, multiplexed assay for superfamily-wide profiling of enzyme activity . Opens in a new window.
Research | 17 November 2010
Quantitative reactivity profiling predicts functional cysteines in proteomes
- Eranthie Weerapana
- , Chu Wang
- , Gabriel M. Simon
- , Florian Richter
- , Sagar Khare
- , Myles B. D. Dillon
- , Daniel A. Bachovchin
- , Kerri Mowen
- , David Baker
- & Benjamin F. Cravatt
Nature 468 , 790–795

Rights & permissionsfor article Quantitative reactivity profiling predicts functional cysteines in proteomes . Opens in a new window.
Research | 15 May 2011
Click-generated triazole ureas as ultrapotent in vivo–active serine hydrolase inhibitors
- Alexander Adibekian
- , Brent R Martin
- , Chu Wang
- , Ku-Lung Hsu
- , Daniel A Bachovchin
- , Sherry Niessen
- , Heather Hoover
- & Benjamin F Cravatt
Nature Chemical Biology 7 , 469–478

Rights & permissionsfor article Click-generated triazole ureas as ultrapotent <i>in vivo</i>–active serine hydrolase inhibitors . Opens in a new window.
Research | 29 March 2009
Identification of selective inhibitors of uncharacterized enzymes by high-throughput screening with fluorescent activity-based probes
Nature Biotechnology 27 , 387–394

Rights & permissionsfor article Identification of selective inhibitors of uncharacterized enzymes by high-throughput screening with fluorescent activity-based probes . Opens in a new window.
Reviews | 3 January 2012
The pharmacological landscape and therapeutic potential of serine hydrolases
- Daniel A. Bachovchin
- & Benjamin F. Cravatt
Nature Reviews Drug Discovery 11 , 52–68

Rights & permissionsfor article The pharmacological landscape and therapeutic potential of serine hydrolases . Opens in a new window.

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Refine your results by…

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Mechanism of filament formation in UPA-promoted CARD8 and NLRP1 inflammasomes

Erratum: Chemoproteomic profiling of host and pathogen enzymes active in cholera

Correction: Corrigendum: Click-generated triazole ureas as ultrapotent in vivo–active serine hydrolase inhibitors

Erratum: Identification of selective inhibitors of uncharacterized enzymes by high-throughput screening with fluorescent activity-based probes

DPP8/9 inhibitors activate the CARD8 inflammasome in resting lymphocytes

DPP8/9 inhibitors are universal activators of functional NLRP1 alleles

DPP8/DPP9 inhibitor-induced pyroptosis for treatment of acute myeloid leukemia

DPP8 and DPP9 inhibition induces pro-caspase-1-dependent monocyte and macrophage pyroptosis

LACTB is a tumour suppressor that modulates lipid metabolism and cell state

Chemoproteomic profiling of host and pathogen enzymes active in cholera

A high-throughput, multiplexed assay for superfamily-wide profiling of enzyme activity

Quantitative reactivity profiling predicts functional cysteines in proteomes

Click-generated triazole ureas as ultrapotent in vivo–active serine hydrolase inhibitors

Identification of selective inhibitors of uncharacterized enzymes by high-throughput screening with fluorescent activity-based probes

The pharmacological landscape and therapeutic potential of serine hydrolases

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