Tetramerization and ATP binding by a protein comprising the A, B, and C domains of rat synapsin I

J Biol Chem. 2004 Mar 19;279(12):11948-56. doi: 10.1074/jbc.M312015200. Epub 2003 Dec 19.

Abstract

Synapsins are multidomain proteins that are critical for regulating neurotransmitter release in vertebrates. In the present study, two crystal structures of the C domain of rat synapsin I (rSynI-C) in complex with Ca(2+) and ATP reveal that this protein can form a tetramer and that a flexible loop (the "multifunctional loop") contacts bound ATP. Further experiments were carried out on a protein comprising the A, B, and C domains of rat synapsin I (rSynI-ABC). An ATP-stabilized tetramer of rSynI-ABC is observed during velocity sedimentation and size-exclusion chromatographic experiments. These hydrodynamic results also indicate that the A and B domains exist in an extended conformation. Calorimetric measurements of ATP binding to wild-type and mutant rSynI-ABC demonstrate that the multifunctional loop and a cross-tetramer contact are important for ATP binding. The evidence supports a view of synapsin I as an ATP-utilizing, tetrameric protein made up of monomers that have a flexible, extended N terminus.

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Amino Acid Sequence
  • Animals
  • Biopolymers
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Binding
  • Protein Conformation
  • Rats
  • Sequence Homology, Amino Acid
  • Synapsins / chemistry
  • Synapsins / metabolism*

Substances

  • Biopolymers
  • Synapsins
  • Adenosine Triphosphate

Associated data

  • PDB/1PK8
  • PDB/1PX2