Credit: Nucleic Acids Research (2025). DOI: 10.1093/nar/gkaf249
New research pioneered by The University of Western Australia is shedding light on the intricate dance between proteins, DNA and RNA—the fundamental building blocks that carry out cellular processes and underpin all life, including plants, humans and bacteria.
Led by Professor Charlie Bond from UWA's School of Molecular Sciences, a team of scientists has contributed to three studies published in Nucleic Acids Research, showcasing unprecedented three-dimensional models of how protein molecular machines assemble on DNA or RNA.
"We've essentially been watching life's machinery in action at the molecular level," Professor Bond said.
"By visualizing how these complex structures assemble and function, we're opening doors to entirely new approaches in diagnostics and therapeutic interventions."
The , helmed by postdoctoral research fellow at the University of Wollongong Nicholas Marzano and UWA researcher Brady Johnston, found that a family of tiny coiled molecules from plants, known as PPR proteins, function like microscopic springs, compressing when they bind to RNA molecules.
"This mechanism allows remarkable precision in molecular targeting within cells and points toward innovative RNA-based diagnostic tools, and potential interventions for genetic disorders or to introduce new traits into plants," Dr. Marzano said.
The , under Ph.D. candidate Heidar Koning and ARC DECRA research fellow Andrew Marshall from UWA's School of Molecular Sciences, in partnership with researchers at Monash University and the University of Melbourne, showed how human proteins NONO and SFPQ form sophisticated complexes that orchestrate gene activity in the cell nucleus.
"These findings provide crucial insights for developing targeted approaches to regulate gene expression in both health and disease states," Koning said.
The , undertaken by Curtin University Research Fellow Dr. Callum Verdonk, in collaboration with Professor Bond and Assistant Professor Josh Ramsay from Curtin University, revealed how a DNA-binding protein called RdfS forms helical structures or twisting forms that control the process of DNA transfer between agricultural bacteria.
"DNA is literally cut out of one bacterium's genome and transferred over to another with the help of RdfS protein," Dr. Verdonk said. "The bacteria can form a symbiosis with plants and are used as an environmentally friendly alternative to chemical fertilizer."
More information: Nicholas Marzano et al, Single-molecule visualization of sequence-specific RNA binding by a designer PPR protein, Nucleic Acids Research (2024).
Heidar J Koning et al, Structural plasticity of the coiled–coil interactions in human SFPQ, Nucleic Acids Research (2024).
Callum J Verdonk et al, Structural basis for control of integrative and conjugative element excision and transfer by the oligomeric winged helix–turn–helix protein RdfS, Nucleic Acids Research (2025).
Journal information: Nucleic Acids Research
Provided by University of Western Australia