The AAA protein spastin possesses two levels of basal ATPase activity

FEBS Lett. 2018 May;592(10):1625-1633. doi: 10.1002/1873-3468.13075. Epub 2018 May 15.

Abstract

The AAA ATPase spastin is a microtubule-severing enzyme that plays important roles in various cellular events including axon regeneration. Herein, we found that the basal ATPase activity of spastin is negatively regulated by spastin concentration. By determining a spastin crystal structure, we demonstrate the necessity of intersubunit interactions between spastin AAA domains. Neutralization of the positive charges in the microtubule-binding domain (MTBD) of spastin dramatically decreases the ATPase activity at low concentration, although the ATP-hydrolyzing potential is not affected. These results demonstrate that, in addition to the AAA domain, the MTBD region of spastin is also involved in regulating ATPase activity, making interactions between spastin protomers more complicated than expected.

Keywords: AAA domain; ATPase; Spastin; microtubule-binding domain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Amino Acid Sequence
  • Binding Sites
  • Crystallography, X-Ray
  • Humans
  • Microtubules / metabolism
  • Protein Binding
  • Protein Domains
  • Protein Multimerization
  • Protein Subunits / metabolism
  • Proteolysis
  • Sequence Homology, Amino Acid
  • Spastin / chemistry
  • Spastin / metabolism*

Substances

  • Protein Subunits
  • Adenosine Triphosphatases
  • Spastin
  • SPAST protein, human

Associated data

  • PDB/3B9P
  • PDB/3VFD
  • PDB/5Z6Q
  • figshare/10.6084/m9.figshare.6177008