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bioRxiv preprint doi: https://doi.org/10.1101/2023.11.15.567102; this version posted November 20, 2023. The copyright holder for this preprint (which was not certified by peer review) is the author/funder,
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01
Identify the target protein or enzyme that you want to screen against.
02
Select a diverse library of small fragment compounds for screening.
03
Set up the screening assay, ensuring it is suitable for fragment binding.
04
Perform the high-throughput screening to assess fragment interactions with the target.
05
Analyze the binding data to find fragments with promising interactions.
06
Optimize hit fragments through medicinal chemistry to improve potency and specificity.
07
Conduct further assays to validate the activity of optimized fragments.

Who needs fragment-based screening targeting an?

01
Pharmaceutical companies developing new drugs.
02
Biotech firms focused on innovative therapeutic solutions.
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Academic researchers studying protein-ligand interactions.
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Teams involved in lead discovery for novel targets.
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Fragment-based screening is a drug discovery technique that identifies small chemical fragments that bind to a biological target, such as a protein, to help in the development of new therapeutics.
Organizations and researchers conducting fragment-based screening studies on biological targets are typically required to file associated reports to regulatory bodies or funding agencies.
To fill out a fragment-based screening filing, one needs to provide information on the target, the fragments used, screening methods, results obtained, and any subsequent optimization performed.
The purpose is to discover potential drug candidates by identifying small molecules that can efficiently bind to target proteins, thus serving as the starting point for further drug development.
Reported information typically includes details about the biological target, fragments tested, experimental conditions, binding affinities, and any follow-up studies conducted based on the initial findings.
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