The solution structure of human mitochondria fission protein Fis1 reveals a novel TPR-like helix bundle

Motoshi Suzuki1, Seon Yong Jeong, Mariusz Karbowski

  • 1Biochemistry Section, Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.

Insights

Human Fis1 protein, crucial for mitochondrial fission, was structurally characterized. Its unique TPR-like fold suggests a molecular adaptor role, though its interaction with Drp1 in cells is regulated.

Area of Science:

  • Biochemistry
  • Cell Biology
  • Structural Biology

Background:

  • Fis1 protein in yeast regulates mitochondrial fission by interacting with Dnm1 and Mdv1.
  • Conserved Fis1 orthologs in higher eukaryotes suggest functional conservation.

Purpose of the Study:

  • To clone and determine the protein structure of the human Fis1 ortholog.
  • To investigate the structural basis for Fis1 function and its interaction with Drp1.

Main Methods:

  • Human Fis1 ortholog cloning.
  • Nuclear Magnetic Resonance (NMR) spectroscopy for protein structure determination.
  • HeLa cell experiments to assess Fis1-Drp1 interaction.

Main Results:

  • The human Fis1 protein structure consists of a flexible N-terminal tail, a six-alpha-helix core domain, and a disordered C-terminal transmembrane segment.
  • The core domain exhibits a TPR-like fold but lacks sequence similarity to typical TPR motifs.
  • Increased mitochondrial Fis1 levels in HeLa cells did not lead to Drp1 translocation, indicating regulated interaction.

Conclusions:

  • Human Fis1 functions as a molecular adaptor on the mitochondrial outer membrane via its TPR-like domain.
  • The interaction between Fis1 and Drp1 is regulated, suggesting complex control over mitochondrial fission.

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