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Visinin-Like Protein-3 Modulates the Interaction Between Cytochrome b 5 and NADH-Cytochrome b 5 Reductase in a Ca2+-Dependent Manner

  • Kensuke Oikawa
  • , Gary L. Odero
  • , Solmaz Nafez
  • , Ning Ge
  • , Dali Zhang
  • , Hiroya Kobayashi
  • , Keisuke Sate
  • , Shoji Kimura
  • , Masatoshi Tateno
  • , Benedict C. Albensi

Research output: Contribution to journalArticlepeer-review

Abstract

Visinin-like proteins (VILIPs) belong to the calcium sensor protein family. VILIP-1 has been examined as a cerebrospinal fluid biomarker and as a potential indicator for cognitive decline in Alzheimer’s disease (AD). However, little is known about VILIP-3 protein biochemistry. We performed co-immunoprecipitation experiments to examine whether VILIP-3 can interact with reduced nicotine adenine dinucleotide (NADH)-cytochrome b5 reductase. We also evaluated the specificity of cytochrome b5 within the visinin-like protein subfamily and identified cytochrome P450 isoforms in the brain. In this study, we show that cytochrome b5 has an affinity for hippocalcin, neurocalcin-δ, and VILIP-3, but not visinin-like protein-1. VILIP-3 was also shown to interact with NADH-cytochrome b5 reductase in a Ca2+-dependent manner. These results suggest that VILIP-3, hippocalcin, and neurocalcin-δ provide a Ca2+-dependent modulation to the NADH-dependent microsomal electron transport. The results also suggest that future therapeutic strategies that target calcium-signaling pathways and VILIPs may be of value.
Original languageEnglish
Pages (from-to)449-457
Number of pages9
JournalCell Biochemistry and Biophysics
Volume74
Issue number4
DOIs
StatePublished - Dec 1 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2016, Springer Science+Business Media New York.

ASJC Scopus Subject Areas

  • Biophysics
  • Biochemistry
  • Cell Biology

Keywords

  • Calcium
  • Calcium sensor
  • Electron transport
  • Mitochondria
  • Molecular
  • Nerve

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