9DHC

The Retinoblastoma Protein with Mutation S751Y

Summary for 9DHC

• Entry DOI: 10.2210/pdb9dhc/pdb
• Related: 4ELL
• Descriptor: Retinoblastoma-associated protein (2 entities in total)
• Functional Keywords: cancer missense mutation, cell cycle
• Biological source: Homo sapiens (human)
• Total number of polymer chains: 2
• Total formula weight: 91229.69

Authors

Ruiz-Rivera, A.,Castro, A.,Burke, J.R. (deposition date: 2024-09-03, release date: 2025-02-19, Last modification date: 2025-03-26)

Primary citation

Castro, A.,Ruiz Rivera, A.,Moorman, C.C.,Wolf-Saxon, E.R.,Mims, H.N.,Vasquez Meza, V.I.,Rangel, M.A.,Loera, M.M.,Bond, I.C.,Buchanan, S.B.,Villarreal, E.,Tripathi, S.,Rubin, S.M.,Burke, J.R.
Structural and functional analysis of cancer-associated missense variants in the retinoblastoma protein pocket domain.
J.Biol.Chem., 301:108284-108284, 2025

PubMed Abstract: The retinoblastoma tumor suppressor (Rb) is a multifunctional protein that primarily regulates the cell cycle but also has roles in cellular differentiation, DNA damage response and apoptosis. The loss of Rb is a key event in the development or progression of many cancers. Essential functions of Rb occur through its pocket domain, which is necessary for regulating binding interactions with E2F transcription factors and transcription repressors that bind via an LxCxE motif. The pocket domain is the most highly-conserved region of the multidomain protein, as well as the most frequent site of mutations. To understand what effects cancer missense mutations have on Rb's pocket domain, we used fluorescence polarization and differential scanning fluorimetry to quantify changes caused by 75 cancer-associated missense variants to E2F transactivation domain (E2F) binding, LxCxE binding, and the thermostability of the pocket domain. We find that 43% of the missense variants tested reduce Rb-E2F binding. Many of these variants are not located at the E2F binding site, yet they destabilize the fold of the protein and show temperature-sensitive binding effects. We also find that 21% of tested mutations reduce LxCxE binding, and several mutations selectively disrupt either E2F or LxCxE binding. Protein X-ray crystallography of four missense variants reveals how mutations destabilize the protein fold and inhibit E2F or LxCxE binding. Taken together, this work provides the first understanding of the multiple ways through which stability, structure and function of Rb's pocket domain are altered by common missense mutations seen in cancer.

PubMed: 39938803
DOI: 10.1016/j.jbc.2025.108284

Experimental method

X-RAY DIFFRACTION (2.32 Å)