Literature DB >> 16413305

Assay and properties of the mitochondrial dynamin related protein Opa1.

Lorena Griparic1, Alexander M van der Bliek.   

Abstract

Opa1, also known as Mgm1 in yeast, is a mitochondrial member of the dynamin family. Unlike other dynamin family members, Opa1 has an N-terminal mitochondrial targeting sequence, suggesting that this protein is imported into mitochondria. Here, we describe biochemical techniques, such as mitochondrial isolation, digitonin extraction, a protease protection assay, and carbonate extraction, that were used to determine that mammalian Opa1 resides in the intermembrane space where it is tightly bound to the inner membrane. In addition, we describe bacterial expression of the Opa1 GTPase domain, methods for purification, and an in vitro assay for GTP hydrolysis.

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Year:  2005        PMID: 16413305     DOI: 10.1016/S0076-6879(05)04054-1

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  4 in total

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Journal:  Methods Mol Biol       Date:  2020

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Authors:  F Alexandra Loucks; Emily K Schroeder; Amelia E Zommer; Shea Hilger; Natalie A Kelsey; Ron J Bouchard; Craig Blackstone; Jay L Brewster; Daniel A Linseman
Journal:  Brain Res       Date:  2008-11-18       Impact factor: 3.252

3.  Mitochondrial-targeted aryl hydrocarbon receptor and the impact of 2,3,7,8-tetrachlorodibenzo-p-dioxin on cellular respiration and the mitochondrial proteome.

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4.  N-terminal cleavage of the mitochondrial fusion GTPase OPA1 occurs via a caspase-independent mechanism in cerebellar granule neurons exposed to oxidative or nitrosative stress.

Authors:  Josie J Gray; Amelia E Zommer; Ron J Bouchard; Nathan Duval; Craig Blackstone; Daniel A Linseman
Journal:  Brain Res       Date:  2012-12-07       Impact factor: 3.252

  4 in total

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