Peptable

Comparison

LL-37 vs MOTS-c

Also see:

LL-37MOTS-c

Function

While LL-37 acts as a broad-spectrum antimicrobial and immunomodulatory peptide involved in host defense and wound repair, but can also promote inflammation and cancer cell proliferation in some contexts5215, MOTS-c improves insulin sensitivity, enhances glycolysis, reduces oxidative stress, and shows protective effects in models of metabolic syndrome, aging, and ischemia-reperfusion injury8135146.

Mechanism

While LL-37 works as a cationic amphipathic 37-amino-acid cathelicidin peptide generated from hCAP18 that disrupts microbial membranes and modulates innate immunity, including chemotaxis, cytokine induction, and NET formation521586, MOTS-c is a 16-amino-acid mitochondrial-derived peptide that translocates to the nucleus under metabolic stress and regulates glucose and lipid metabolism largely via activation of AMPK and modulation of mTOR and folate-cycle–linked pathways854140146.

Receptor

LL-37

Functions as a ligand for CXCR2 on neutrophils and other myeloid cells; LL-37 signaling has also been linked to FPR2 and P2X7 in various cell types515

MOTS-c

No dedicated cell-surface receptor has been definitively identified; signaling is primarily described via intracellular AMPK and related metabolic pathways8135146

Organism or Origin

LL-37

Human cathelicidin antimicrobial peptide generated from the CAP-18 precursor5286

MOTS-c

Human mitochondrial peptide encoded in the 12S rRNA gene region54146

Gene

LL-37

CAMP

MOTS-c

MT-RNR1

Summary

LL-37 and MOTS-c are noticeably different, with limited direct overlap in their usual biological context. Their typical research and application settings separate fairly clearly: LL-37 is more often discussed in the realm of Immunology and inflammation and Gastroenterology, whereas MOTS-c is more often associated with the realm of Metabolic and endocrine and Aging and longevity. They also influence different molecular systems, with LL-37 tracking more closely to GPCR receptor while MOTS-c centers more on Mitochondrial membrane. LL-37 has a more natural endogenous origin, while MOTS-c is closer to mitochondrial-encoded background and both are still best understood as being in Preclinical development. Their sequence patterns also diverge, with LL-37 showing cationic amphipathic and alpha-helical domain features and MOTS-c showing hydrophobic domain features.

Related articles

No related articles are linked to these peptides yet.

Sources

52Cathelicidin LL-37: A new important molecule in the ... - PMC - NIH, https://pmc.ncbi.nlm.nih.gov/articles/PMC7388365/
86Cathelicidin antimicrobial peptide - Wikipedia, https://en.wikipedia.org/wiki/Cathelicidin_antimicrobial_peptide
8Mitochondrial-encoded peptide MOTS-c prevents pancreatic islet ..., https://www.nature.com/articles/s12276-025-01521-1
54MOTS-c - Wikipedia, https://en.wikipedia.org/wiki/MOTS-c
135MOTS-c Promotes Glycolysis via AMPK-HIF-1α-PFKFB3 ... - PubMed, https://pubmed.ncbi.nlm.nih.gov/40035775/
146MOTS-c: A promising mitochondrial-derived peptide for therapeutic ..., https://pmc.ncbi.nlm.nih.gov/articles/PMC9905433/