A study showed that researchers had estimated a "computational microscope" that can simulate the atomic and subatomic forces that drive molecular interactions. This tool will streamline efforts to understand the chemistry of life, model large molecular systems and develop new pharmaceutical and industrial agents. The study was published in the journal Nature Methods.

The scientists combined two computational approaches used to simulate molecular interactions. The first, a nanoscale molecular-dynamics program known as NAMD, uses classical-mechanics methods to model the structure and simulate the behavior of hundreds of millions of individual atoms.

The second program zooms in on the subatomic realm, simulating the interactions of protons, neutrons, and electrons. Modeling at this quantum-mechanical scale demands a lot of computational power, so the researchers implemented a method for partitioning large molecules into classical- and quantum-mechanics regions.

This allows them to focus their computational resources on small regions involved in critical interactions, such as the making or breaking of chemical bonds. Both molecular mechanics and quantum mechanics programs have been available for years, and other teams have worked to combine them. But the new effort streamlines the process of setting up, performing and analyzing the simulations.

"We set it up so that researchers can easily choose how they will partition their systems," Luthey-Schulten said. "My students are trying it out, and most of them can do it without much difficulty." Schulten developed NAMD at Illinois in 1995, combining it with visualization software, VMD, which enables researchers to watch large-scale molecular interactions unfold.

The computational microscope is ideal for modeling structural traits and motions of large complexes. That simulation accounted for the interactions of more than 64 million atoms and required the use of the Blue Waters supercomputer. The new study also made use of Blue Waters, this time to improve the resolution of the computational microscope.

The NAMD software is designed to describe the behavior of individual atoms. But individual atoms involved in specific chemical interactions and reactions don't always behave like their counterparts elsewhere. Understanding how they vary requires a closer look at the subatomic forces at play.

As a demonstration of the new approach, the researchers simulated the chemical behavior of transfer RNAs, molecules that play a key role in translating genetic information into proteins. Using NAMD, they modeled the overall molecular structure of tRNA at the moment that a special protein loads an amino acid to the tRNA.

They partitioned two sites of the complex into regions requiring the more focused quantum mechanical approach. The subatomic simulations of the interactions of the two regions allowed the team to run simulations of four different scenarios that would allow the tRNA to function as it does in the cell.

Their simulations revealed that one of the four potential chemical pathways was more energetically favorable than the others and thus more likely to occur. The researchers also used various methods to partition the tRNA complex between the MM and QM regions and reported on each approach.

They did not pick just one way; we picked as many as possible. How you structure it depends on the particular system you're studying," said Rafael Bernardi."NAMD was designed and this was my husband's vision to treat really large systems. "Now we can add the subatomic scale to that, opening up vast new possibilities for research."