Compounds derived from Humulus lupulus inhibit SARS-CoV-2 papain-like protease and virus replication

Anna-Maria Herzog; Katharina Göbel; Luigi Marongiu; Natalia Ruetalo; Marta Campos Alonso; Christian Leischner; Christian Busch; Markus Burkard; Ulrich M Lauer; Paul P Geurink; Klaus-Peter Knobeloch; Michael Schindler; Günter Fritz; Sascha Venturelli

doi:10.1016/j.phymed.2023.155176

Compounds derived from Humulus lupulus inhibit SARS-CoV-2 papain-like protease and virus replication

Phytomedicine. 2024 Jan:123:155176. doi: 10.1016/j.phymed.2023.155176. Epub 2023 Oct 30.

Affiliations

¹ Department of Cellular Microbiology, University of Hohenheim, 70599 Stuttgart, Germany.
² Department of Internal Medicine VIII, University Hospital Tuebingen, 72076 Tuebingen, Germany; Department of Nutritional Biochemistry, University of Hohenheim, 70599 Stuttgart, Germany.
³ Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen, 72076 Tuebingen, Germany.
⁴ Institute of Neuropathology, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
⁵ Department of Nutritional Biochemistry, University of Hohenheim, 70599 Stuttgart, Germany.
⁶ Dermatologie zum Delfin, 8400 Winterthur, Switzerland.
⁷ Department of Internal Medicine VIII, University Hospital Tuebingen, 72076 Tuebingen, Germany.
⁸ Department of Cell and Chemical Biology, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands.
⁹ Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen, 72076 Tuebingen, Germany. Electronic address: michael.schindler@med.uni-tuebingen.de.
¹⁰ Department of Cellular Microbiology, University of Hohenheim, 70599 Stuttgart, Germany. Electronic address: guenter.fritz@uni-hohenheim.de.
¹¹ Department of Nutritional Biochemistry, University of Hohenheim, 70599 Stuttgart, Germany; Institute of Physiology, Department of Vegetative and Clinical Physiology, University Hospital Tuebingen, 72076 Tuebingen, Germany. Electronic address: sascha.venturelli@uni-hohenheim.de.

PMID: 37976697
DOI: 10.1016/j.phymed.2023.155176

Abstract

Background: Selected natural compounds exhibit very good antiviral properties. Especially, the medicinal plant Humulus lupulus (hop) contains several secondary plant metabolites some of which have previously shown antiviral activities. Among them, the prenylated chalcone xanthohumol (XN) demonstrated to be a potent inhibitor of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (M^pro).

Hypothesis/purpose: Following the finding that xanthohumol (XN) is a potent inhibitor of SARS-CoV-2 M^pro, the effect of XN and its major derivatives isoxanthohumol (IXN), 6-prenylnaringenin (6-PN), and 8-prenylnaringenin (8-PN) from hops on SARS-CoV-2 papain-like protease (PL^pro) were investigated.

Study design: The modulatory effect of the hop compounds on PL^pro were studied first in silico and then in vitro. In addition, the actual effect of hop compounds on the replication of SARS-CoV-2 in host cells was investigated.

Methods: In silico docking analysis was used to predict the binding affinity of hop compounds to the active site of PL^pro. A recombinant PL^pro was cloned, purified, characterized, and analyzed by small-angle X-ray scattering (SAXS), deISGylation assays, and kinetic analyses. Antiviral activity of hop compounds was assessed using the fluorescently labeled wildtype SARS-CoV-2 (icSARS-CoV-2-mNG) in Caco-2 host cells.

Results: Our in silico docking suggests that the purified hop compounds bind to the active site of SARS-CoV-2 PL^pro blocking the access of its natural substrates. The hop-derived compounds inhibit SARS-CoV-2 PL^pro with half maximal inhibitory concentration (IC₅₀) values in the range of 59-162 µM. Furthermore, we demonstrate that XN and 6-PN, in particular, impede viral replication with IC₅₀ values of 3.3 µM and 7.3 µM, respectively.

Conclusion: In addition to the already known inhibition of M^pro by XN, our results show, for the first time, that hop-derived compounds target also SARS-CoV-2 PL^pro which is a promising therapeutic target as it contributes to both viral replication and modulation of the immune system. These findings support the possibility to develop new hop-derived antiviral drugs targeting human coronaviruses.

Keywords: COVID-19; Hop compounds; Papain-like protease; SARS-CoV-2; Viral proteases; Xanthohumol.

MeSH terms

Antiviral Agents / chemistry
Antiviral Agents / pharmacology
COVID-19*
Caco-2 Cells
Coronavirus Papain-Like Proteases*
Flavonoids*
Humans
Humulus* / chemistry
Molecular Docking Simulation
Propiophenones*
SARS-CoV-2
Scattering, Small Angle
Virus Replication
X-Ray Diffraction

Substances

xanthohumol
papain-like protease, SARS-CoV-2
Antiviral Agents
Coronavirus Papain-Like Proteases
Flavonoids
Propiophenones