First atom-level structure of packaged viral genome reveals new properties and dynamics

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First atom-level structure of packaged viral genome reveals new properties, dynamics
Simulation of genome packaging. a, Top, packaging of the HK97 genome at 4 bp per 2 bead resolution. Bottom, the plots illustrate simulations of the packaging process (left) driven by the portal potential (inset) and of spontaneous ejection (right). Solid lines here and throughout the figure depict ensemble averages; shaded regions depict the s.e.m. among eight independent packaging simulations (replicas) for each curve. b, Internal pressure and energy during packaging and equilibration (Equil.) simulations. c, Switchback-loop formation during packaging. Inset depicts a switchback loop with a highly curved center and two arms that remain within 6 nm. The three genome configurations depict the formation of two switchback loops (in cyan and green). The first switchback loop (cyan) is extruded by the packaging motor until growth of the loop stalls and the nascently packaged DNA buckles, forming a second loop (green). The DNA is colored by the instantaneous bend energy from 0 kcal mol−1 (red) to 1.5 kcal mol−1 (blue). d, Quantification of switchback loops during packaging, including the absolute number of loops detected, the average loop length (note that loops may overlap) and the amount of the packaged DNA in at least one switchback loop. e, Global order in the packaged genome. The local nematic order (6 nm neighborhood), and the Frank–Oseen nematic energy calculated from the nematic director field. f, Toroidal order of the packaged genome. g, Example of a packaged genome featuring a baseball seam interface between early-packaged (blue) and late-packaged (red) DNA. h, Streamlines of the nematic director field of select capsids reveal a distinct pattern for each genome. Each streamline is colored by the local nematic order with white corresponding to zero order, and blue corresponding to the maximum order observed in the system. Credit: Nature (2024). DOI: 10.1038/s41586-024-07150-4

A computational model of the more than 26 million atoms in a DNA-packed viral capsid expands our understanding of virus structure and DNA dynamics, insights that could provide new research avenues and drug targets, University of Illinois Urbana-Champaign researchers report in the journal Nature.

“To fight a virus, we want to know everything there is to know about it. We know what’s inside in terms of components, but we don’t know how they’re arranged,” said study leader Aleksei Aksimentiev, an Illinois professor of physics. “Knowledge of the internal structures gives us more targets for drugs, which tend to focus on receptors on the surface or replication proteins.”

Viruses keep their genetic material—either DNA or RNA—packaged in a hollow particle called a capsid. While the structures of many hollow capsids have been described, the structure of a full capsid and the genetic material inside it has remained elusive.

For this first look at a complete packaged viral genome, the researchers focused on HK97, a virus that infects bacteria. It has been well-studied experimentally, so the Illinois group would be able to compare its simulations to what has been found previously, said Aksimentiev, who also is affiliated with the Beckman Institute of Advanced Science and Technology at Illinois.

“We know from experiments that the capsid has a portal, and there is a motor protein there that pushes the DNA in. We also know the structure of the capsid from experiments. We know the genetic sequence, but what was not known was the structure of the packaged genetic material inside.”






Credit: University of Illinois at Urbana-Champaign

Figuring out the structural dynamics of genome packaging has challenged researchers for several reasons. It cannot yet be seen experimentally, so simulation on a supercomputer is required. However, a simulation can either show great detail for a very short time or less detail for a longer time.

The Illinois group developed a multiresolution approach to DNA simulation, looking at the problem at multiple levels of resolution and time length and putting all the information together to get a complete picture of the process. Having previously used and validated it in experiments involving DNA origami, they now applied the multiresolution approach to HK97.

The result was the first atom-level look at the viral DNA packaging process and the structural properties and fluctuations when the DNA is fully contained in the capsid.

They found that the DNA formed switchback loops as it was pushed into the capsid, an important finding as it is similar to how DNA is organized in eukaryotic cells. They also found that the DNA organized itself into domains conforming to the topology of the capsid. The process resulted in slightly different configurations of loops and topologies of DNA in each particle simulated.






Credit: University of Illinois at Urbana-Champaign

“These differences show that the concept of individuality is not exclusive to animals and plants but extends down to viruses, the most primitive form of gene-replicating structures,” Aksimentiev said. “This opens another dimension to looking at infectivity and whether these differences among viruses account for variability in their ability to infect.”

The simulations did reveal common structural features and defects, particularly at the edges and corners of the capsid, where its shape has the greatest influence on the DNA inside. These features could be potential targets for drug development, Aksimentiev said.

“We believe this is just the beginning for our methodology, the first study to look at the structure of a viral genome,” Aksimentiev said. “With bigger, faster computers and more knowledge from experiments, we will eventually be able to computationally resolve the structures of genomes from other viral species, including RNA viruses, which are more complicated as they self-assemble.”

“The more we know about these viruses, the more we can combat them or harness them for applications such as combating bacteria that have grown resistant to antibiotic use,” Aksimentiev said.

More information:
Aleksei Aksimentiev, The structure and physical properties of a packaged bacteriophage particle, Nature (2024). DOI: 10.1038/s41586-024-07150-4. www.nature.com/articles/s41586-024-07150-4

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University of Illinois at Urbana-Champaign

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First atom-level structure of packaged viral genome reveals new properties and dynamics (2024, March 6)
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