Iron–sulfur clusters as inhibitors and catalysts of viral replication

Kourosh Honarmand Ebrahimi*, Simone Ciofi-Baffoni, Peter Leon Hagedoorn, Yvain Nicolet, Nick E. Le Brun, Wilfred R. Hagen, Fraser A. Armstrong

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

20 Citations (Scopus)
32 Downloads (Pure)

Abstract

A virus hijacks host cellular machineries and metabolites in order to reproduce. In response, the innate immune system activates different processes to fight back. Although many aspects of these processes have been well investigated, the key roles played by iron–sulfur [FeS] clusters, which are among the oldest classes of bio-inorganic cofactors, have barely been considered. Here we discuss how several [FeS] cluster-containing proteins activate, support and modulate the innate immune response to restrict viral infections, and how some of these proteins simultaneously support the replication of viruses. We also propose models of function of some proteins in the innate immune response and argue that [FeS] clusters in many of these proteins act as biological ‘fuses’ to control the response. We hope this overview helps to inspire future research in the emerging field of bio-inorganic virology/immunology and that such studies may reveal new molecular insight into the links between viral infections and diseases like cancer and neurodegeneration. [Figure not available: see fulltext.]

Original languageEnglish
Pages (from-to)253-266
Number of pages14
JournalNature Chemistry
Volume14
Issue number3
DOIs
Publication statusPublished - 2022

Bibliographical note

Green Open Access added to TU Delft Institutional Repository 'You share, we take care!' - Taverne project https://www.openaccess.nl/en/you-share-we-take-care
Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.

Fingerprint

Dive into the research topics of 'Iron–sulfur clusters as inhibitors and catalysts of viral replication'. Together they form a unique fingerprint.

Cite this