Live cell screening to identify RNA-binding small molecule inhibitors of the pre-let-7–Lin28 RNA–protein interaction

Author:

Rosenblum Sydney L.1ORCID,Soueid Dalia M.2,Giambasu George3ORCID,Vander Roest Steve4,Pasternak Alexander5,DiMauro Erin F.5,Simov Vladimir5ORCID,Garner Amanda L.12ORCID

Affiliation:

1. Program in Chemical Biology, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI, 48109, USA

2. Department of Medicinal Chemistry, College of Pharmacy, University of Michigan, 1600 Huron Parkway, NCRC B520, Ann Arbor, MI 48109, USA

3. Computational Chemistry, Merck & Co., Inc., Boston, MA 02115, USA

4. Center for Chemical Genomics, Life Sciences Institute, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI, 48109, USA

5. Discovery Chemistry, Merck & Co., Inc., Boston, MA 02115, USA

Abstract

Dysregulation of the networking of RNA-binding proteins (RBPs) and RNAs drives many human diseases, including cancers, and the targeting of RNA–protein interactions (RPIs) has emerged as an exciting area of RNA-targeted drug discovery.

Funder

Merck Sharp and Dohme Italia

National Institute of General Medical Sciences

Publisher

Royal Society of Chemistry (RSC)

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