Inhibition of virally induced TFEB proteasomal degradation as a host-centric therapeutic approach for coronaviral infection

The endolysosomal pathway plays an evolutionarily conserved role in pathogen clearance, and viruses have evolved complex mechanisms to evade this host defense system. Here, we describe a previously unidentified aspect of coronaviral infection, whereby the master transcriptional activator of lysosomal homeostasis-TFEB-is targeted for proteasomal-mediated degradation upon viral infection. Through mass spectrometry analysis and an unbiased small interfering RNA screen, we identify that TFEB protein stability is coordinately regulated by the E3 ubiquitin ligase subunit DCAF7 and the PAK2 kinase. We derive a series of novel small molecules that interfere with the DCAF7-TFEB interaction. These agents inhibit virus-induced TFEB degradation and demonstrate broad antiviral activities including attenuating severe acute respiratory syndrome coronavirus 2 infection in two animal models. Together, these results delineate a virally triggered pathway that impairs lysosomal homeostasis in the host. Small molecule E3 ubiquitin ligase DCAF7 inhibitors that restore lysosomal function represent a novel class of host-directed, antiviral therapies useful for current and potentially future coronaviral variants.

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Publication Details

Journal
Science Advances
Published
2025-06-06
DOI
https://doi.org/10.1126/sciadv.adv4033
Citations
5
Primary Topic
Cell death mechanisms and regulation
Type
article
Field-Weighted Citation Impact
4.03
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article

Inhibition of virally induced TFEB proteasomal degradation as a host-centric therapeutic approach for coronaviral infection

Ferhan Tuncer, Michael M. Myerburg, Karina C. Lockwood, Toren Finkel et al.
5 citations
Science Advances
Cell death mechanisms and regulation
4.03
article

Inhibition of virally induced TFEB proteasomal degradation as a host-centric therapeutic approach for coronaviral infection

Ferhan Tuncer, Michael M. Myerburg, Karina C. Lockwood, Toren Finkel, Claudette M. St. Croix, Laura Salminen, Travis Lear, Áine N. Boudreau, Simon M. Barratt‐Boyes, J. Villandre, Jason R. Kennerdell, Irene Alfaras, Benjamin R. Treat, Mads Larsen, Yusuke Sekine, Xiaojun Tan, Bo Lin, Bill B. Chen, Yuan Liu, Jie Liu, Jing Ma, Yanwen Chen, Yao Tong, Qing Cao, Daniel P. Camarco, Lucas Hertzel, John W. Evankovich
article en
5 citations

Abstract

The endolysosomal pathway plays an evolutionarily conserved role in pathogen clearance, and viruses have evolved complex mechanisms to evade this host defense system. Here, we describe a previously unidentified aspect of coronaviral infection, whereby the master transcriptional activator of lysosomal homeostasis-TFEB-is targeted for proteasomal-mediated degradation upon viral infection. Through mass spectrometry analysis and an unbiased small interfering RNA screen, we identify that TFEB protein stability is coordinately regulated by the E3 ubiquitin ligase subunit DCAF7 and the PAK2 kinase. We derive a series of novel small molecules that interfere with the DCAF7-TFEB interaction. These agents inhibit virus-induced TFEB degradation and demonstrate broad antiviral activities including attenuating severe acute respiratory syndrome coronavirus 2 infection in two animal models. Together, these results delineate a virally triggered pathway that impairs lysosomal homeostasis in the host. Small molecule E3 ubiquitin ligase DCAF7 inhibitors that restore lysosomal function represent a novel class of host-directed, antiviral therapies useful for current and potentially future coronaviral variants.

Science AdvancesVol. 11(23)
University of Pittsburgh (US)
Good health and well-being
Openalex Percentile: Top 6%
Cell death mechanisms and regulation
4.03
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