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Computer simulation of protein synthesis reveals high complexity of cell machinery

20-Mar-2017

Osaka University

Growth and collapse of the network composed of QSS components. Circle indicates the QSS component and line indicates the connection between the components.

Osaka University

Developed a large-scale whole component protein synthesis translation simulator.

Osaka University

A result of protein synthesis simulation. Concentration changes of 241 components are shown.

Life depends on proteins. These molecules are produced continually in our cells, which act as microscopic production lines - but the process is so complex we have barely begun to understand it. Exploring protein synthesis may, however, be the key to revealing how the body controls the thousands of reactions occurring simultaneously inside us.

Now, a Japanese research team led by Osaka University and RIKEN has run a computer simulation of a small protein (peptide) being produced by bacterial translation machinery, confirming a "molecular toolkit" as highly sophisticated even for simple lifeforms.

Full-size proteins are too large to model in detail. However, a tripeptide (made from three amino acids: "Met-Gly-Gly") can be produced by a set of 27 molecules in the bacteria E. coli. The researchers simulated this process, also known as an in-vitro translation (IVT), by modeling the chemical reactions on a computer.

Even for this simple tripeptide, over 900 reactions were needed, with over 200 chemicals formed as by-products. These reactions occurred at wildly different speeds, and the slowest acted as bottlenecks on the overall process. The researchers found some reaction rates from earlier experiments, while others had to be assumed. Then, they simulated 1,000 seconds of the resulting chemical dance.

"We were surprised that even with so many assumptions and simplifications, the simulation accurately described the kinetics of Met-Gly-Gly production," study lead author Tomoaki Matsuura says. "When we increased the amounts of some initial components, the rate of synthesis increased, in line with real IVT."

By tracking the amount of each chemical present, the researchers found that many chemicals reached a stable level (termed steady-state), however, only to suddenly decrease again later on. In fact, this collapse happened twice - after 0.5 sec and again after 10 sec.

The researchers believe this non-linear behavior, wherein chemicals reach a "stable state" in the system, but are later recruited back to "active state", is typical of biochemistry.

"The peak, collapse, and further peaking of steady states is likely to occur in other processes, such as glucose metabolism," Matsuura says.

Matsuura adds that the simulations could be extended to different proteins, including larger ones. "By comparing our simulations with IVT experiments," he says, "we can improve the IVT systems - which in turn will help us improve the simulations. The awesome complexity of this 'simple' synthesis reminds us that we are just beginning to understand life at the molecular level."

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