Target intelligence / Profile preview

Adenine nucleotide translocator 1 (ANT1) (ANT1)

Target
ANT1
Molecular classification
Transporter, Mitochondrial carrier family, Solute carrier family 25, Mitochondrial permeability transition pore component
01

Overview

Adenine nucleotide translocator 1 (ANT1), also known as ADP/ATP translocase 1, is a nuclear-encoded protein located in the inner mitochondrial membrane that plays a fundamental role in cellular energy metabolism [1, 10]. It functions as an antiporter, exchanging mitochondrial ATP for cytosolic ADP, thereby ensuring a continuous supply of energy for cellular processes while maintaining the pool of substrates for oxidative phosphorylation [12]. Beyond its transport function, ANT1 is a critical component or regulator of the mitochondrial permeability transition pore (mPTP), making it a central player in the execution of apoptosis [3, 6]. Mutations in the SLC25A4 gene, which encodes ANT1, are associated with various mitochondrial disorders such as progressive external ophthalmoplegia and Senger's syndrome, often involving mitochondrial DNA deletions and muscle dysfunction [13, 15]. In the context of drug development, ANT1 is considered a potential target for cancer therapy due to its ability to trigger cell death when modulated by specific ligands or pro-apoptotic proteins like Bax [8, 11]. However, the high expression of ANT1 in the heart and skeletal muscle poses significant safety challenges, as unintended inhibition can lead to severe cardiomyopathy and metabolic failure [14, 16].

Other names
ADP/ATP translocase 1Solute carrier family 25 member 4AAC1T1ADP,ATP carrier protein 1Heart/skeletal muscle ATP/ADP translocatorANT1
02

Mechanism of action

Inhibition of ADP/ATP exchange and modulation of the mitochondrial permeability transition pore (mPTP) to induce apoptosis [3, 6, 12].

03

Biological functions

ADP/ATP exchangeMitochondrial uncouplingApoptosis regulationMitochondrial DNA maintenanceThermogenesis
04

Disease associations

Progressive external ophthalmoplegiaSenger's syndromeMitochondrial DNA depletion syndromeCardiomyopathyCancerFacioscapulohumeral muscular dystrophy
05

Safety considerations

Mitochondrial myopathy [4, 15]Hypertrophic cardiomyopathy [13]Disruption of cellular energy homeostasis [9, 16]Lactic acidosis [13]
06

Interacting drugs

Atractyloside

5 more in the full profile.

07

Biomarkers

Mitochondrial DNA deletions [13]ANT1 protein expression levels [14]Mitochondrial reactive oxygen species (ROS) [14]Serum lactic acid levels [13]

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