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Title: Insights into RNA binding by the anticancer drug cisplatin from the crystal structure of cisplatin-modified ribosome

Journal Article · · Nucleic Acids Research
DOI:https://doi.org/10.1093/nar/gkw246· OSTI ID:1258691

Cisplatin is a widely prescribed anticancer drug, which triggers cell death by covalent binding to a broad range of biological molecules. Among cisplatin targets, cellular RNAs remain the most poorly characterized molecules. Although cisplatin was shown to inactivate essential RNAs, including ribosomal, spliceosomal and telomeric RNAs, cisplatin binding sites in most RNA molecules are unknown, and therefore it remains challenging to study how modifications of RNA by cisplatin contributes to its toxicity. Here we report a 2.6Å-resolution X-ray structure of cisplatin-modified 70S ribosome, which describes cisplatin binding to the ribosome and provides the first nearly atomic model of cisplatin–RNA complex. We observe nine cisplatin molecules bound to the ribosome and reveal consensus structural features of the cisplatin-binding sites. Two of the cisplatin molecules modify conserved functional centers of the ribosome—the mRNA-channel and the GTPase center. In the mRNA-channel, cisplatin intercalates between the ribosome and the messenger RNA, suggesting that the observed inhibition of protein synthesis by cisplatin is caused by impaired mRNA-translocation. Furthermore, our structure provides an insight into RNA targeting and inhibition by cisplatin, which can help predict cisplatin-binding sites in other cellular RNAs and design studies to elucidate a link between RNA modifications by cisplatin and cisplatin toxicity.

Research Organization:
Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities Division; National Inst. of Health
Grant/Contract Number:
AC02-06CH11357; GM022778; GM022854; P41GM103403
OSTI ID:
1258691
Journal Information:
Nucleic Acids Research, Vol. 44, Issue 10; ISSN 0305-1048
Publisher:
Oxford University PressCopyright Statement
Country of Publication:
United States
Language:
ENGLISH
Citation Metrics:
Cited by: 48 works
Citation information provided by
Web of Science

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Cited By (15)

Intercalation‐enhanced “Click” Crosslinking of DNA journal November 2018
Intercalation‐enhanced “Click” Crosslinking of DNA journal November 2018
Amino acid-linked platinum(II) compounds: non-canonical nucleoside preferences and influence on glycosidic bond stabilities journal July 2019
Oxidation and alkylation stresses activate ribosome-quality control journal December 2019
Differences in cisplatin distribution in sensitive and resistant ovarian cancer cells: a TEM/NanoSIMS study journal January 2017
Unexpected therapeutic effects of cisplatin journal January 2019
Stabilizing DNA nanostructures through reversible disulfide crosslinking journal January 2019
Aminoglycoside interactions and impacts on the eukaryotic ribosome journal December 2017
How do cells cope with RNA damage and its consequences? journal August 2019
Effect of curcumin nanoparticles on the cisplatin-induced neurotoxicity in rat journal September 2018
Effects of Pycnogenol on cisplatin-induced optic nerve injury: an experimental study journal September 2018
Granulin A Synergizes with Cisplatin to Inhibit the Growth of Human Hepatocellular Carcinoma journal October 2018
Fingerprinting CANDO: Increased Accuracy with Structure- and Ligand-Based Shotgun Drug Repurposing journal October 2019
PAC1 Receptor Mediates Electroacupuncture-Induced Neuro and Immune Protection During Cisplatin Chemotherapy journal September 2021
Protein Synthesis Inhibition and Activation of the c-Jun N-Terminal Kinase Are Potential Contributors to Cisplatin Ototoxicity journal September 2017

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