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In this way, the drug is not freely administrated, and the carriers slowly release the drug in circulation, which could eventually bind endogenous immunophilins

Zhang Q., Yan L., Lu J., Zhou X

New MI, Ghizzoni L, Meyer-Bahlburg H, Khattab A, Reichman D, Rosenwaks Z

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Its a perfect example of how a seemingly minor tweak in an amino acid sequence can create a profoundly different tool for researchers

Rather than disrupting the binding pocket directly, the biotin modification extends through a solvent accessible pore formed at this loop (amino acids 5963) from the protein surface distal to the binding pocket (Supplementary Fig