NMR Studies of Retroviral Genome Packaging

Author/Creator ORCID

Date

2020-09-30

Department

Program

Citation of Original Publication

Boyd, Patricia S.; Brown, Janae B.; Brown, Joshua D.; Catazaro, Jonathan; Chaudry, Issac; Ding, Pengfei; Dong, Xinmei; Marchant, Jan; O’Hern, Colin T.; Singh, Karndeep; Swanson, Canessa; Summers, Michael F.; Yasin, Saif; NMR Studies of Retroviral Genome Packaging; Viruses 2020, 12(10), 1115; https://www.mdpi.com/1999-4915/12/10/1115

Rights

This item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.
Attribution 4.0 International (CC BY 4.0)

Subjects

Abstract

Nearly all retroviruses selectively package two copies of their unspliced RNA genomes from a cellular milieu that contains a substantial excess of non-viral and spliced viral RNAs. Over the past four decades, combinations of genetic experiments, phylogenetic analyses, nucleotide accessibility mapping, in silico RNA structure predictions, and biophysical experiments were employed to understand how retroviral genomes are selected for packaging. Genetic studies provided early clues regarding the protein and RNA elements required for packaging, and nucleotide accessibility mapping experiments provided insights into the secondary structures of functionally important elements in the genome. Three-dimensional structural determinants of packaging were primarily derived by nuclear magnetic resonance (NMR) spectroscopy. A key advantage of NMR, relative to other methods for determining biomolecular structure (such as X-ray crystallography), is that it is well suited for studies of conformationally dynamic and heterogeneous systems—a hallmark of the retrovirus packaging machinery. Here, we review advances in understanding of the structures, dynamics, and interactions of the proteins and RNA elements involved in retroviral genome selection and packaging that are facilitated by NMR.