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Lane, Amy L

0000-0002-8386-364X

Mayo Clinic

Department of Cancer Biology, Mayo Clinic, Jacksonville, FL 32224, USA.

Citations 3

A Virtual Screening Platform Identifies Chloroethylagelastatin A as a Potential Ribosomal Inhibitor
Caulfield, Thomas R. , Hayes, Karen E., Qiu, Yushi, Coban, Matt , Lane, Amy L. , Yoshimitsu, Takehiko , Hazlehurst, Lori , Copland, John A. , Coban, Mathew, Lane, Amy L , Tun, Han W. , Caulfield, Thomas R , Coban, Mathew A , Oh, Joon Seok

Biomolecules | October 5, 2020 | Volume: 10 | Issue: 10 | Pages: 1407

10.3390/biom10101407 Get It

Chloroethylagelastatin A (CEAA) is an analogue of agelastatin A (AA), a natural alkaloid derived from a marine sponge. It is under development for therapeutic use against brain tumors as it has excellent central nervous system (CNS) penetration and pre-clinical therapeutic activity against brain tumors. Recently, AA was shown to inhibit protein synthesis by binding to the ribosomal A-site. In this study, we developed a novel virtual screening platform to perform a comprehensive screening of various AA analogues showing that AA analogues with proven therapeutic activity including CEAA have significant ribosomal binding capacity whereas therapeutically inactive analogues show poor ribosomal binding and revealing structural fingerprint features essential for drug-ribosome interactions. In particular, CEAA was found to have greater ribosomal binding capacity than AA. Biological tests showed that CEAA binds the ribosome and contributes to protein synthesis inhibition. Our findings suggest that CEAA may possess ribosomal inhibitor activity and that our virtual screening platform may be a useful tool in discovery and development of novel ribosomal inhibitors.
Optimization of Peptide Hydroxamate Inhibitors of Insulin-Degrading Enzyme Reveals Marked Substrate-Selectivity
Abdul‐Hay, Samer O., Lane, Amy L. , Caulfield, Thomas R. , Claussin, Clémence , Bertrand, Juliette , Masson, Amandine, Choudhry, Shakeel, Fauq, Abdul H. , Maharvi, Guhlam M., Leissring, Malcolm A. , Caulfield, Thomas R , Lane, Amy L

Journal of Medicinal Chemistry | February 25, 2013 | Volume: 56 | Issue: 6 | Pages: 2246-2255

10.1021/jm301280p Get It