$80

Peptides
MOTS-C
Mitochondrial Open Reading Frame of 12S rRNA-c, mitochondria-derived peptide. Supplied as a lyophilised powder in 10mg and 40mg vials.
Supplied as lyophilised powder in 10mg, 40mg specifications. Storage: -20°C · Keep dry, avoid light. Dispatched from Sydney, Australia-wide.
Product information
About MOTS-C
Mitochondrial Open Reading Frame of 12S rRNA-c
Research background as published in the scientific literature. Supplied for in-vitro laboratory research only; nothing here is a claim about use in humans or animals.
MOTS-C (Mitochondrial Open Reading Frame of 12S rRNA-c) is a mitochondria-derived peptide encoded in the mitochondrial genome's 12S rRNA region. First identified in 2015 by Lee et al., it represents a class of mitochondria-derived peptides (MDPs) that function as metabolic regulators.
Research has focused on MOTS-C's role in metabolic signalling, with particular interest in its interactions with nuclear gene expression. Studies suggest it may translocate to the nucleus under stress conditions to modulate gene transcription. Investigations into its potential effects on healthy ageing, obesity-related metabolic dysfunction, and exercise adaptation continue to make it an active subject of preclinical research.
- Origin
- Mitochondria-derived peptide
- Research Areas
- Metabolic signalling, insulin sensitivity, exercise
- Amino Acids
- 16 residues
- Molecular Weight
- ~2.17 kDa
- First Identified
- 2015 — Lee et al.
- Key Pathway
- AMPK · FOXO · PPAR
- Research Models
- Murine metabolic models
- Status
- Preclinical research
- 01AMPK ActivationMOTS-C has been shown to activate AMPK (AMP-activated protein kinase), a master regulator of cellular energy homeostasis. Research investigates downstream effects on glucose uptake, fatty acid oxidation, and mitochondrial biogenesis.
- 02Insulin SensitivityLaboratory studies have examined MOTS-C's effects on insulin signalling pathways, including PI3K/AKT activation and GLUT4 translocation. Research models suggest potential roles in glucose regulation and insulin resistance.
- 03Exercise MimeticResearch has investigated MOTS-C as an exercise mimetic, with studies reporting effects on endurance capacity and metabolic adaptation in preclinical models. Its mitochondrial origin distinguishes it from other metabolic peptides.
References
- 1Lee C et al. The mitochondrial-derived peptide MOTS-c promotes metabolic homeostasis and reduces obesity and insulin resistance. Cell Metab. 2015;21(3):443-454.
- 2Reynolds JC et al. MOTS-c is an exercise-induced mitochondrial-encoded regulator. Nat Commun. 2021;12:470.
- 3PubMed: pubmed.ncbi.nlm.nih.gov/?term=MOTS-C+peptide
- 4Kim SJ et al. Mitochondrially derived peptides as novel regulators of metabolism. J Physiol. 2017;595(21):6613-6621.
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