The protein, CaMKII, is ubiquitous in cells throughout the body but is perhaps best known for its prominent role in the brain and the heart. It is critical in learning and memory but, if misregulated, can cause problems.
“The most powerful engine to drive new discoveries on CaMKII functions may lie in the availability of three distinct classes of pharmacological inhibitors,” said the manuscript’s senior author, Ulli Bayer, Ph.D., professor of pharmacology at the CU School of Medicine. “These inhibitors now allow a detailed first assessment of CaMKII functions in any given system in a way that is readily accessible to a broad range of scientists without specialized interest in CaMKII research.”
Carolyn Nicole Brown, a graduate student working in Bayer’s laboratory, co-authored the manuscript.
Filling in the gaps
Previous studies by Bayer’s lab revealed that inhibiting CaMKII activity protects against some of the effects of amyloid-beta (Abeta) plaques in the brain, a hallmark of Alzheimer’s disease (AD).
The researchers found one group of inhibitors, or drugs, that protected from the Abeta effects without detrimental side effects, making it potentially useful in treating a number of brain diseases.
Yet CaMKII is present in nearly every other cell. The review offers insights into the protein for those who don’t study it full-time, providing tools to fill in the gaps in knowledge about how the protein functions.
“We are experts in studying this complex protein, and here we provide a guideline for non-specialists to use these new tools,” Bayer said. “We are trying to make it easier for everyone.”
Brown, the co-author, agreed. “The most important advances will be filling the gaps that we don’t even know about yet,” she said.
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References/Sources/Materials provided by:
This article was written by David Kelly at the University of Colorado Anschutz Medical Campus
http://dx.doi.org/10.1016/j.celrep.2024.113982
https://www.cell.com/cell-reports/fulltext/S2211-1247(24)00310-3
