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Control of biochemical reactions through supramolecular RING domain self-assembly.

RING domains act in a variety of unrelated biochemical reactions, with many of these domains forming key parts of supramolecular assemblies in cells. Here, we observe that purified RINGs from a variety of functionally unrelated proteins, including promyelocytic leukemia protein, KAP-1TIF1beta, Z, Mel18, breast cancer susceptibility gene product 1 (BRCA1), and BRCA1-associated RING domain (BARD1), self-assemble into supramolecular structures in vitro that resemble those they form in cells. RING bodies form polyvalent binding surfaces and scaffold multiple partner proteins. Separation of RING bodies from monomers reveals that self-assembly controls and amplifies their specific activities in two unrelated biochemistries: reduction of 5' mRNA cap affinity of eIF4E by promyelocytic leukemia protein and Z, and E3 ubiquitin conjugation activity of BARD1:BRCA1. Functional significance of self-assembly is underscored by partial restoration of assembly and E3 activity of cancer predisposing BRCA1 mutant by forced oligomerization. RING self-assembly creates bodies that act structurally as polyvalent scaffolds, thermodynamically by amplifying activities of partner proteins, and catalytically by spatiotemporal coupling of enzymatic reactions. These studies reveal a general paradigm of how supramolecular structures may function in cells.

Pubmed ID: 12438698

Authors

  • Kentsis A
  • Gordon RE
  • Borden KL

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Data

November 26, 2002

Associated Grants

  • Agency: NCI NIH HHS, Id: CA 80728
  • Agency: NCI NIH HHS, Id: CA 88991

Mesh Terms

  • Animals
  • BRCA1 Protein
  • Breast Neoplasms
  • Carrier Proteins
  • Catalysis
  • Cattle
  • Cells
  • DNA-Binding Proteins
  • Eukaryotic Initiation Factor-4E
  • Genes, BRCA1
  • Humans
  • Immediate-Early Proteins
  • Ligases
  • Macromolecular Substances
  • Membrane Proteins
  • Mice
  • Models, Biological
  • Mutation
  • Neoplasm Proteins
  • Nuclear Proteins
  • Protein Binding
  • Protein Folding
  • Protein Structure, Tertiary
  • RNA Caps
  • Rabbits
  • Repressor Proteins
  • Structure-Activity Relationship
  • Thermodynamics
  • Transcription Factors
  • Tumor Suppressor Proteins
  • Ubiquitin
  • Ubiquitin-Conjugating Enzymes
  • Ubiquitin-Protein Ligases
  • Zinc