Post by leadXpro AG

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๐—›๐—ผ๐˜„ ๐—ฌ๐—ผ๐˜‚๐—ฟ ๐— ๐—ผ๐—ฟ๐—ป๐—ถ๐—ป๐—ด ๐—–๐—ผ๐—ณ๐—ณ๐—ฒ๐—ฒ ๐—ง๐—ฒ๐—ฎ๐—ฐ๐—ต๐—ฒ๐˜€ ๐—จ๐˜€ ๐—”๐—ฏ๐—ผ๐˜‚๐˜ ๐—ฅ๐—ฒ๐—ฐ๐—ฒ๐—ฝ๐˜๐—ผ๐—ฟ ๐—ฆ๐—ฐ๐—ถ๐—ฒ๐—ป๐—ฐ๐—ฒ This short video illustrates two key concepts in pharmacology โ€” agonists and antagonists โ€” using adenosine and caffeine binding to neuronal adenosine receptors. While adenosine (the agonist) activates the receptor, caffeine (the antagonist) blocks it. In collaboration with Jรถrg Standfuss' team at PSI Paul Scherrer Institut, our colleague Hannah Glover studies the A2A adenosine receptor with time-resolved serial crystallography experiments using both synchrotrons and XFELs, to better understand receptor and ligand binding dynamics at the molecular level. We foresee the knowledge obtained would improve the structure-based drug discovery process for challenging membrane protein targets. A great example of how everyday molecules can illuminate cutting-edge research! ๐Ÿ”— https://lnkd.in/dGuxUGwK #leadxpro #PSI #adenosine #crystallography

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