Researchers from the the Monash University in Australia offer new hope to thousands of people who experience heart attacks and heart failure - one of the major causes of death worldwide.
They showed new insights into a specific protein belonging to the family of G protein-coupled receptors (GPCRs).
After successfully combining two molecules, they say they are a step closer to creating a brand new class of drug that is more targeted and could possess minimal side effects.
Almost half of all current medications available use GPCRs to achieve their therapeutic effect.
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Current GPCR drugs work either by fully activating or completely blocking receptors, treating the protein like a simple "on-off" switch.
The new research discovered alternative recognition sites on GPCRs that can be targeted by drugs to fine-tune the behaviour of the protein, basically converting the "on-off" switch into a "dimmer switch".
"Correct dosage has been a serious challenge in clinical trials for A1 receptor drugs. The consequences are serious; a dosage that is too high can stop the heart from beating. Too low, and the drug fails to prevent cell damage. Getting this balance right has been a big problem," said researcher Peter Scammells.
The study was published in the journal PNAS.