Inorganic polyphosphate (polyP) as an activator and structural component of the mitochondrial permeability transition pore

Maria E. Solesio, Pia A. Elustondo, Eleonora Zakharian, Evgeny Pavlov

Research output: Contribution to journalArticle

Abstract

Mitochondrial permeability transition pore (mPTP) is a large channel located in the mitochondrial inner membrane. The opening of mPTP during pathological calcium overload leads to the membrane depolarization and disruption of ATP production. mPTP activation has been implicated as a central event during the process of stress-induced cell death. mPTP is a supramolecular complex composed of many proteins. Recent studies suggest that mitochondrial ATPase plays the central role in the formation of mPTP. However, the structure of the central conducting pore part of mPTP (mPTPore) remains elusive. Here we review current models proposed for the mPTPore and involvement of polyP in its formation and regulation. We discuss the underestimated role of polyP as an effector and a putative structural component of the mPTPore. We propose the hypothesis that inclusion of polyP can explain such properties of mPTP activity as calcium activation, selectivity and voltage-dependence.

Original languageEnglish (US)
Pages (from-to)7-12
Number of pages6
JournalBiochemical Society Transactions
Volume44
DOIs
StatePublished - Feb 15 2016

Fingerprint

Polyphosphates
Chemical activation
Calcium
Membranes
Depolarization
Mitochondrial Membranes
Cell death
mitochondrial permeability transition pore
Adenosine Triphosphatases
Cell Death
Adenosine Triphosphate
Electric potential

Keywords

  • Calcium
  • Inorganic polyphosphate (polyp)
  • Mitochondria
  • Permeability transition

ASJC Scopus subject areas

  • Biochemistry

Cite this

Inorganic polyphosphate (polyP) as an activator and structural component of the mitochondrial permeability transition pore. / Solesio, Maria E.; Elustondo, Pia A.; Zakharian, Eleonora; Pavlov, Evgeny.

In: Biochemical Society Transactions, Vol. 44, 15.02.2016, p. 7-12.

Research output: Contribution to journalArticle

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