A molecular dynamics simulation study of an aminoglycoside/A-site RNA complex: conformational and hydration patterns

• Published in: Biochimie Vol. 88; no. 8; pp. 1061 - 1073
• Main Authors: Vaiana, A.C., Westhof, E., Auffinger, P.
• Format: Journal Article
• Language: English
• Published: France Elsevier Masson SAS 01-08-2006; Elsevier
• Subjects: Aminoglycoside; Aminoglycosides - chemistry; Aminoglycosides - pharmacology; Anti-Bacterial Agents - chemistry; Anti-Bacterial Agents - pharmacology; Antibiotic; Binding Sites; Biochemistry, Molecular Biology; Computer Simulation; Crystallography, X-Ray - methods; Drug design; Hydration; Life Sciences; Ligand binding; Models, Molecular; Molecular dynamics simulation; Nucleic Acid Conformation - drug effects; Paromomycin - chemistry; Paromomycin - pharmacology; Ribosome; RNA, Ribosomal, 16S - chemistry; Solvation; Thermodynamics; Ligand binding; Antibiotic; Ribosome; Solvation; Hydration; Aminoglycoside; Drug design; Molecular dynamics simulation
• ISSN: 0300-9084; 1638-6183
• DOI: 10.1016/j.biochi.2006.06.006

Aminoglycoside antibiotics interfere with the translation mechanism by binding to the tRNA decoding site of the 16S ribosomal RNA. Crystallographic structures of aminoglycosides bound to A-site systems clarified many static aspects of RNA–ligand interactions. To gain some insight on the dynamic aspects of recognition phenomena, we conducted molecular dynamics simulations of the aminoglycoside paromomycin bound to a eubacterial ribosomal decoding A-site oligonucleotide. Results from 25 ns of simulation time revealed that: (i) the neamine part of the antibiotic represents the main anchor for binding, (ii) additional sugar rings provide limited and fragile contacts, (iii) long-resident water molecules present at the drug/RNA interface are involved in the recognition phenomena. The combination of MD simulations together with systematic structural information offers striking insights into the molecular recognition processes underlying RNA/aminoglycoside binding. Important methodological considerations related to the use of medium resolution starting structures and associated sampling problems are thoroughly discussed.