Accession Number : AD1048000


Title :   Inhibition of Retinoblastoma Protein Inactivation


Descriptive Note : Technical Report,01 Sep 2014,31 Aug 2017


Corporate Author : University of California, Santa Cruz Santa Cruz United States


Personal Author(s) : Rubin, Seth M


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/1048000.pdf


Report Date : 01 Nov 2017


Pagination or Media Count : 16


Abstract : The objective of this project is to discover and characterize molecules that inhibit breast cancer cell proliferation by maintaining activity of the retinoblastoma protein (Rb). Rb is inactivated to drive proliferation in normal and cancer cells by phosphorylation, which dissociates the E2F transcription factor from Rb to activate S phase genes. Our goal is to find and characterize molecules that stabilize the complex between phosphorylated Rb and E2F. During the project period, we tested our proposed mechanism for how molecules may enhance the affinity of phosphorylated Rb (phosRb) for E2F by disrupting the compact phosRb conformation. We identified a proof-of-concept peptide that increases phosRb-affinity, we developed a fluorescence-based assay to identify small molecule enhancers of phos-Rb affinity, we performed a high throughput screen and further tested hits in the primary screen, and we began pursuing additional fragment-based approaches to identifying lead compounds.


Descriptors :   proteins , transcription factors , xray crystallography , inhibition , breast cancer , assays , modulation , fluorescence


Subject Categories : Medicine and Medical Research
      Genetic Engineering and Molecular Biology
      Biochemistry


Distribution Statement : APPROVED FOR PUBLIC RELEASE