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GHK-Cu

Copper Tripeptide-1, Glycyl-L-Histidyl-L-Lysine Copper, Prezatide Copper

Quick Stats
Studies 149
Trials 1
Score 1
2025 pubmed 1 citations

Self-Assembled Peptide-Gold Nanoparticle 1D Nanohybrids Functionalized with GHK Tripeptide for Enhanced Wound-Healing and Photothermal Therapy.

Jeon. Nayeong N; Kim. Leeseo L; Choi. Seong Gyu SG; Lee. Hyunseung H; Min. Jin Young JY; Kim. Hye Min HM; Han. Eun Hee EH; Lee. Eunji E

Key Findings

  • GHK alone heals wounds but breaks down quickly in the body.
  • Embedding GHK in self‑assembled peptide nanofibers with 3 nm gold particles creates a stable hybrid that absorbs near‑infrared light efficiently.
  • The hybrid can both speed up wound repair and destroy cancer cells under infrared illumination, thanks to its photothermal effect.

Practical Outcomes

  • For biohackers, the study doesn’t provide a ready‑to‑use protocol or dosage. It mainly shows that future medical products might combine GHK with nanotechnology for better stability and added cancer‑killing ability, but the current method is far beyond DIY capabilities.

Summary

Scientists made a tiny hybrid material that mixes a wound‑healing peptide (GHK) with gold nanoparticles. By arranging the peptide into nanofibers, they kept the gold particles stable and made the whole thing good at both healing cuts and killing cancer cells when hit with infrared light. The work shows a clever way to improve GHK’s stability, but it requires advanced lab techniques that aren’t practical for DIY use.

Abstract

Glycyl-l-histidyl-l-lysine (GHK) tripeptides are known for their remarkable therapeutic potential, including wound-healing, anti-inflammatory activity, and cellular regeneration. However, their clinical application has been significantly hindered by poor biological stability and limited efficacy in a physiological medium. In this study, we introduce a sophisticated approach to overcome these limitations by developing supramolecular peptide nanofiber-gold (Au) nanoparticle (NP) hybrids functionalized with GHK tripeptides. By strategically manipulating peptide self-assembly and NP integration, we demonstrated a useful platform that enhances both therapeutic efficacy and material stability. Our methodology involves the precise engineering of 9-fluorenylmethoxycarbonyl-diphenylalanine scaffolds with GHK and KHG tripeptides, enabling robust nanofibril formation through π-π stacking and hydrogen bonding. Critically, we discovered that the specific amino acid sequence significantly influences the surface exposure of lysine, directly impacting the nanohybrid's wound-healing capabilities. The resultant nanohybrids exhibit exceptional characteristics: Au NPs are spatially confined within the peptide nanofibers, achieving a remarkably uniform size distribution of approximately 3 nm. These nanohybrids demonstrate superior near-infrared (NIR) light absorption and photothermal conversion efficiency, enabling effective eradication of cancer cells and organoids killing under NIR irradiation. This dual-functional nanohybrid integrates biocompatible and enzymatically degradable peptide scaffolds to achieve synergistic wound-healing and cancer-killing effects. By mitigating the cytotoxicity and biodegradability issues associated with conventional photothermal agents, our system provides a promising strategy to improve postoperative cancer therapy and promote tissue regeneration. This work highlights the potential of peptide-inorganic nanohybrids in advancing multifunctional therapeutic platforms for cancer treatment and tissue repair.

Study Information

Provider

pubmed

Year

2025

Date

2025-02-28T00:00:00.000Z

DOI

10.1021/acsami.4c21924

Citations

1

References

59