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Targeting the alternative oxidase (AOX) for human health and food security, a pharmaceutical and agrochemical target or a rescue mechanism?
Szibor, Marten; Schenkl, Christina; Barsottini, Mario R O; Young, Luke; Moore, Anthony L.
Afiliación
  • Szibor M; Department of Cardiothoracic Surgery, and Center for Sepsis Control and Care (CSCC), Jena University Hospital, DE-07747 Jena, Germany.
  • Schenkl C; Faculty of Medicine and Health Technology, Tampere University, FI-33520 Tampere, Finland.
  • Barsottini MRO; Department of Cardiothoracic Surgery, and Center for Sepsis Control and Care (CSCC), Jena University Hospital, DE-07747 Jena, Germany.
  • Young L; Biochemistry & Biomedicine, School of Life Sciences, University of Sussex, Brighton BN1 9QG, U.K.
  • Moore AL; Genomics and BioEnergy Laboratory, Institute of Biology, University of Campinas, Campinas - SP 13083-862, Brazil.
Biochem J ; 479(12): 1337-1359, 2022 06 30.
Article en En | MEDLINE | ID: mdl-35748702
ABSTRACT
Some of the most threatening human diseases are due to a blockage of the mitochondrial electron transport chain (ETC). In a variety of plants, fungi, and prokaryotes, there is a naturally evolved mechanism for such threats to viability, namely a bypassing of the blocked portion of the ETC by alternative enzymes of the respiratory chain. One such enzyme is the alternative oxidase (AOX). When AOX is expressed, it enables its host to survive life-threatening conditions or, as in parasites, to evade host defenses. In vertebrates, this mechanism has been lost during evolution. However, we and others have shown that transfer of AOX into the genome of the fruit fly and mouse results in a catalytically engaged AOX. This implies that not only is the AOX a promising target for combating human or agricultural pathogens but also a novel approach to elucidate disease mechanisms or, in several cases, potentially a therapeutic cure for human diseases. In this review, we highlight the varying functions of AOX in their natural hosts and upon xenotopic expression, and discuss the resulting need to develop species-specific AOX inhibitors.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Agroquímicos / Proteínas Mitocondriales Límite: Animals / Humans Idioma: En Revista: Biochem J Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Agroquímicos / Proteínas Mitocondriales Límite: Animals / Humans Idioma: En Revista: Biochem J Año: 2022 Tipo del documento: Article País de afiliación: Alemania