Structural determinants of MALT1 protease activity

J Mol Biol. 2012 May 25;419(1-2):4-21. doi: 10.1016/j.jmb.2012.02.018. Epub 2012 Feb 23.

Abstract

The formation of the CBM (CARD11-BCL10-MALT1) complex is pivotal for antigen-receptor-mediated activation of the transcription factor NF-κB. Signaling is dependent on MALT1 (mucosa-associated lymphoid tissue lymphoma translocation protein 1), which not only acts as a scaffolding protein but also possesses proteolytic activity mediated by its caspase-like domain. It remained unclear how the CBM activates MALT1. Here, we provide biochemical and structural evidence that MALT1 activation is dependent on its dimerization and show that mutations at the dimer interface abrogate activity in cells. The unliganded protease presents itself in a dimeric yet inactive state and undergoes substantial conformational changes upon substrate binding. These structural changes also affect the conformation of the C-terminal Ig-like domain, a domain that is required for MALT1 activity. Binding to the active site is coupled to a relative movement of caspase and Ig-like domains. MALT1 binding partners thus may have the potential of tuning MALT1 protease activity without binding directly to the caspase domain.

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Amino Acid Sequence
  • Animals
  • B-Cell CLL-Lymphoma 10 Protein
  • Caspases / chemistry*
  • Caspases / metabolism*
  • Catalytic Domain
  • Cells, Cultured
  • Dimerization
  • Enzyme Activation
  • HEK293 Cells
  • Humans
  • Ligands
  • Mice
  • Models, Molecular
  • Molecular Sequence Data
  • Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein
  • Mutation
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Neoplasm Proteins / chemistry*
  • Neoplasm Proteins / metabolism*
  • Protein Binding
  • Protein Interaction Domains and Motifs / genetics
  • Protein Structure, Tertiary
  • Receptors, Antigen / chemistry
  • Receptors, Antigen / genetics
  • Receptors, Antigen / metabolism
  • Signal Transduction
  • Structure-Activity Relationship

Substances

  • Adaptor Proteins, Signal Transducing
  • B-Cell CLL-Lymphoma 10 Protein
  • BCL10 protein, human
  • Ligands
  • NF-kappa B
  • Neoplasm Proteins
  • Receptors, Antigen
  • Caspases
  • MALT1 protein, human
  • Malt1 protein, mouse
  • Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein

Associated data

  • PDB/3V4L
  • PDB/3V4O
  • PDB/3V55