Researchers reveal new information about Protein Kinase A

Oct 10 2014

Using X-rays and neutron beams, a team of researchers from the University of California, San Diego School of Medicine, University of Utah and Oak Ridge National Laboratory have teased out new information about Protein Kinase A (PKA), a ubiquitous master switch that helps regulate fundamental cellular functions like energy consumption and interactions with hormones, neurotransmitters and drugs.

"Mutations in PKA can lead to a variety of different human diseases, including cancers, metabolic and cardiovascular diseases and diseases involving the brain and nervous system," said senior author Susan Taylor, PhD, professor of chemistry, biochemistry and pharmacology at UC San Diego and international authority on PKA. "Developing treatments and cures for these diseases depends upon knowing how the switch works."

Writing in the October 10 issue of the Journal of Biological Chemistry, Taylor and colleagues focused on one of four forms of PKA called "II-beta," which is found mostly in the brain and in fat, where it may play an important role in obesity and diet-induced insulin-resistance associated with type 2 diabetes.

All forms of PKA are controlled by a signaling molecule called cyclic AMP or cAMP. Many cellular functions are based upon changing amounts of cAMP within cells. PKA is the molecular sensor for cAMP, modulating cell activity according to cAMP levels.

The scientists investigated which parts of the II-beta protein were needed to determine its overall shape, internal architecture and ability to change shape – factors that dictate function. II-beta is very compact when inactive but extends and separates into subunits when it senses cAMP.

"A key question regarding the architecture of the II-beta was whether both of its cAMP-sensing mechanisms were needed for the unique changes in shape that it undergoes with cAMP," said first author Donald K. Blumenthal, PhD, associate professor of pharmacology and toxicology at the University of Utah College of Pharmacy.

Researchers removed one of II-beta's cAMP sensors and then documented its ability to change shape in response to cAMP, using small-angle X-ray and advanced neutron scattering imaging technologies at Oak Ridge's High Flux Isotope Reactor in Tennessee. They found the protein could still change shape with just one sensor and that its internal architecture remained similar to II-beta protein with both its cAMP sensors.

The findings further narrow and define the key components of II-beta and identify new regions for further investigation. Taylor said the collaborative, multi-team effort also demonstrated the importance of using different techniques in an iterative way to unravel the dynamic properties of complex systems.

Source: University of California - San Diego