Mitochondrial Haemoglobin Is Upregulated with Hypoxia in Skeletal Muscle and Has a Conserved Interaction with ATP Synthase and Inhibitory Factor 1

Author:

Ebanks Brad1,Katyal Gunjan1,Taylor Chris2,Dowle Adam2ORCID,Papetti Chiara3,Lucassen Magnus4ORCID,Moisoi Nicoleta5ORCID,Chakrabarti Lisa16ORCID

Affiliation:

1. School of Veterinary Medicine and Science, University of Nottingham, Nottingham NG7 2RD, UK

2. Department of Biology, Bioscience Technology Facility, University of York, York YO10 5DD, UK

3. Biology Department, University of Padova, 35122 Padova, Italy

4. Alfred Wegener Institute, 27568 Bremerhaven, Germany

5. Leicester School of Pharmacy, Leicester Institute for Pharmaceutical Innovation, De Montfort University, The Gateway, Leicester LE1 9BH, UK

6. MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, Liverpool L7 8TX, UK

Abstract

The globin protein superfamily has diverse functions. Haemoglobin has been found in non-erythroid locations, including within the mitochondria. Using co-immunoprecipitation and in silico methods, we investigated the interaction of mitochondrial haemoglobin with ATP synthase and its associated proteins, including inhibitory factor 1 (IF1). We measured the expression of mitochondrial haemoglobin in response to hypoxia. In vitro and in silico evidence of interactions between mitochondrial haemoglobin and ATP synthase were found, and we report upregulated mitochondrial haemoglobin expression in response to hypoxia within skeletal muscle tissue. Our observations indicate that mitochondrial pH and ATP synthase activity are implicated in the mitochondrial haemoglobin response to hypoxia.

Funder

Biotechnology and Biological Sciences Research Council

University of Nottingham Vice Chancellor’s International Scholarship award

Publisher

MDPI AG

Subject

General Medicine

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