Structural Perspective into the Interaction of an Oncogenesis‐Relevant pre‐miRNA G‐Quadruplex Ligand Carrier with the Protein Nucleolin

Author:

Santos Tiago1ORCID,Silva Micael1ORCID,Imbert Lionel23,Campello Maria P. C.4,Paulo António4,Amrane Samir5,Salgado Gilmar F.5,Cruz Carla16ORCID,Cabrita Eurico J.78ORCID

Affiliation:

1. CICS-UBI – Health Sciences Research Centre University of Beira Interior Av. Infante D. Henrique 6200-506 Covilhã Portugal

2. Institut de Biologie Structurale (IBS) Univ. Grenoble Alpes, CNRS, CEA 38044 Grenoble France

3. EMBL Integrated Structural Biology Grenoble (ISBG) Univ. Grenoble Alpes, CNRS, CEA 38044 Grenoble France

4. Centro de Ciências e Tecnologias Nucleares, Instituto Superior Técnico Universidade de Lisboa Estrada Nacional 10 (km 139,7) 2695-066 Bobadela LRS Portugal

5. ARNA Laboratory, Inserm U1212, CNRS UMR 5320, IECB Université de Bordeaux Pessac 33607 France

6. Departamento de Química, Faculdade de Ciências Universidade da Beira Interior Rua Marquês de Ávila e Bolama 6201-001 Covilhã Portugal

7. UCIBIO, Chemistry Department, NOVA School of Science and Technology Universidade Nova de Lisboa 2829-516 Caparica Portugal

8. Associate Laboratory i4HB – Institute for Health and Bioeconomy NOVA School of Science and Technology Universidade Nova de Lisboa 2829-516 Caparica Portugal

Abstract

AbstractThe structural determinants of the interaction of the G‐quadruplex (G4) motif found in precursor miRNA 149 (rG4) with the acridine orange derivative C8, a G4 ligand stabilizer possessing anticancer activity, and the protein nucleolin (overexpressed in cancer cells) were investigated by Nuclear Magnetic Resonance (NMR) spectroscopy. For the rG4/C8 complex, the results revealed a strong stabilizing interaction between the aromatic core and the iodinated ring of the C8 ligand with the rG4 structure. The NMR study revealed also different interaction patterns between nucleolin and rG4 and nucleolin and rG4/C8 complex. In the absence of the ligand, rG4 establishes interactions with polar residues of the protein while for the rG4/C8 complex, these contacts are mainly established with amino acids that have hydrophobic side chains. However, nucleolin chemical shift perturbation studies in the presence of rG4 or rG4/C8 reveal the same location between domains 1 and 2 of the protein, which suggests that the rG4 and rG4/C8 complex bind in this region. This puzzling structural study opens a new framework to study rG4/ligand/nucleolin complexes that might impact the biogenesis of miRNA 149.

Funder

Fundação para a Ciência e a Tecnologia

French Infrastructure for Integrated Structural Biology

Communauté Université Grenoble Alpes

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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