Protein-RNA complexation driven by the charge regulation mechanism
- 1. Laboratoire de Biochimie Theórique, UPR 9080 CNRS, Institut de Biologie Physico Chimique, Université Paris Diderot – Paris 7 et Université Sorbonne Paris Cité, 13 rue Pierre et Marie Curie, 75005 Paris (France)
- 2. Departamento de Física e Química, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Av. do café, s/no. – Universidade de São Paulo, BR-14040-903 Ribeirão Preto, SP (Brazil)
- 3. Laboratoire de Cristallographie et RMN Biologiques, UMR 8015 CNRS, Faculté des sciences pharmaceutiques et biologiques, Universtié Paris Descartes et Université Sorbonne Paris Cité, 4 Avenue de l'Observatoire, 75006 Paris (France)
Description
Highlights: • Simplified computer models can aid the understanding of complex molecular mechanisms in Structural Biology. • The complexation between the p19 viral protein and the 19-bp small interfering RNA is driven by electrostatic interactions. • Optimal complexation was found at pH 6.5 in agreement with fluorescence experiments. • The charge regulation mechanism plays a pivotal role in this protein-RNA association. • Our outcomes exemplify the importance of constant-pH simulations to proper describe the main fundamental physical mechanisms. Electrostatic interactions play a pivotal role in many (bio)molecular association processes. The molecular organization and function in biological systems are largely determined by these interactions from pure Coulombic contributions to more peculiar mesoscopic forces due to ion-ion correlation and proton fluctuations. The latter is a general electrostatic mechanism that gives attraction particularly at low electrolyte concentrations. This charge regulation mechanism due to titrating amino acid and nucleotides residues is discussed here in a purely electrostatic framework. By means of constant-pH Monte Carlo simulations based on a fast coarse-grained titration proton scheme, a new computer molecular model was devised to study protein–RNA interactions. The complexation between the RNA silencing suppressor p19 viral protein and the 19-bp small interfering RNA was investigated at different solution pH and salt conditions. The outcomes illustrate the importance of the charge regulation mechanism that enhances the association between these macromolecules in a similar way as observed for other protein-polyelectrolyte systems typically found in colloidal science. Due to the highly negative charge of RNA, the effect is more pronounced in this system as predicted by the Kirkwood-Shumaker theory. Our results contribute to the general physico-chemical understanding of macromolecular complexation and shed light on the extensive role of RNA in the cell's life.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2017.07.027Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2017.07.027;
- PII
- S0006291X1731358X;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 498
- Journal Issue
- 2
- Journal Page Range
- p. 264-273
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54056583
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- AMINO ACIDS; MONTE CARLO METHOD; PROTEINS; PROTONS; RNA; SALTS
- Descriptors DEC
- BARYONS; CALCULATION METHODS; CARBOXYLIC ACIDS; ELEMENTARY PARTICLES; FERMIONS; HADRONS; NUCLEIC ACIDS; NUCLEONS; ORGANIC ACIDS; ORGANIC COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Inc. All rights reserved.