Phospholipase A2 are enzymes that play a significant role in many inflammatory diseases including asthma, arthritis and atherosclerosis. This could mean that the PLA2 inhibitors could represent a new class of anti-inflammatory medication.
To better understand PLA2 enzymes and help drive therapeutic drug development, researchers at University of California, San Diego School of Medicine developed 3D computer models that show exactly how two PLA2 enzymes extract their substrates from cellular membranes. The new tool is described in a paper published online the week of Jan. 26 by the Proceedings of the National Academy of Sciences.
"This is the first time experimental data and supercomputing technology have been used to visualize an enzyme interacting with a membrane," said Edward A. Dennis, PhD, Distinguished Professor of Pharmacology, chemistry and biochemistry and senior author of the study. "In doing so, we discovered that binding the membrane triggers a conformational change in PLA2 enzymes and activates them. We also saw several important differences between the two PLA2 enzymes we studied - findings that could influence the design and development of specific PLA2 inhibitor drugs for each enzyme."
Make no mistake, though - the animations of PLA2 in action are not mere cartoons. They are sophisticated molecular dynamics simulations based upon previously published deuterium exchange mass spectrometry (DXMS) data on PLA2. DXMS is an experimental laboratory technique that provides molecular information about the interactions of these enzymes with membranes.
"The combination of rigorous experimental data and in silico [computer] models is a very powerful tool - the experimental data guided the development of accurate 3D models, demonstrating that these two scientific fields can inform one another," Mouchlis said.
The liberation of arachidonic acid by PLA2 enzymes, as shown in these simulations, sets off a cascade of molecular events that result in inflammation. Aspirin and many other anti-inflammatory drugs work by inhibiting enzymes in this cascade that rely on PLA2 enzymes to provide them with arachidonic acid. That means PLA2 enzymes could potentially also be targeted to dampen inflammation at an earlier point in the process.
Co-authors include Denis Bucher, UC San Diego, and J. Andrew McCammon, UC San Diego and Howard Hughes Medical Institute.
This research was funded, in part, by the National Institute of General Medical Sciences at the National Institutes of Health (grants GM20501 and P41GM103712-S1), National Science Foundation (grant ACI-1053575) and Howard Hughes Medical Institute.