
As a undergraduate student, every microbiology/biochem professor i ever had relentlessly drilled into our heads: ATP=energy. Written in my notes on the side margin (and going round and round through my head as i crammed for tests ignored until the last minute) was: ATP=energy, ATP=energy, ATP=energy.
It's true, cells all over our body use Adenosine triphosphate for energy by ripping off one of the phosphate groups somehow (kinda had to reach back to remember that fact.) But, after decades of research into ATP receptor molecules, it seems there is a new way to look at our old familiar adenosine.
It turns out, ATP can act as a chemical messenger as well as a source of cellular energy (this has been postulated since the 70s, but only recently widely accepted.) Dr. Geoffrey Burnstock first proved it, as he observed ATP acting outside of cell boundaries, tansmitting impulses from nerve cell to nerve cell.
Dr. Baljit Khakh's recent work uncovering ATP receptors all over the body has led to researchers in this field to believe that ATP signals not only between nerve cells in the brain, but in nerve tissue attached to other organs. It turns out, ATP mediates signaling for bone building, heart contractions, intestinal contraction, bladder contraction, wound healing, and pain sensing.
Now, we know that ATP receptors mediate certain medical conditions such as cystic fibrosis, inflammation, pain, arrhythmia, chrone's disease, and literally countless others.
In 2009,the structure of P2X, the ATP receptor for pain, was successfully modeled. The next step is to develop drugs that treat pain caused by inflammation. The potential is huge here--if every ATP receptor in the P2 class could be modeled, many elusive medical conditions could finally be treated.
Looks like it's time to ditch the old academic mantra.
How does ATP=versatile sound?
[source--Sci Am "The Double Life of ATP"]