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Tripeptide-1

GHK, Glycyl-L-Histidyl-L-Lysine

Quick Stats
Studies 27
Trials 5
2019 pubmed 20 citations

Formation of Giant and Small Cyclic Complexes from a Flexible Tripeptide Ligand Controlled by Metal Coordination and Hydrogen Bonds.

Miyake. Ryosuke R; Ando. Akira A; Ueno. Manami M; Muraoka. Takahiro T

Key Findings

  • A flexible tripeptide can coordinate with Ni(II) ions to form giant cyclic complexes with cavities about 2 nm across.
  • The size of the ring can be tuned by altering metal coordination, producing smaller versions with cavities up to ten‑fold smaller.
  • These metal‑peptide rings exist both in crystals and in solution, as shown by light scattering and mass spectrometry.

Practical Outcomes

  • For biohackers and self‑experimenters, this study does not provide any actionable health protocol, dosage guidance, or performance‑enhancing insight. It is a materials‑science demonstration that the tripeptide can serve as a scaffold for metal‑based nanostructures, which may be of interest only to those designing novel delivery vehicles or sensors, not to everyday longevity or performance optimization.

Summary

Scientists showed that a tiny three‑amino‑acid chain (a tripeptide) can be linked together with nickel ions to build large ring‑shaped structures that have tiny cavities inside. By changing how the metal and hydrogen bonds attach, they can make the rings bigger or smaller, but the work is purely about chemistry and material design, not about any health benefit.

Abstract

Formation of giant cyclic complexes by the assembly of small, flexible units is demonstrated by connecting 14 artificial tripeptides (1) with 14 Ni(II) ions. Although tripeptide 1 is very flexible because of the presence of three CH<sub>2</sub> groups in the main chain, it formed a tetradecanuclear cyclic complex ([1<sub>14</sub>Ni<sub>14</sub>]<sup>28+</sup>) with a large cavity (diameter: ca. 2 nm). In this structure, three tripeptides are coordinated to each Ni(II) center by three different coordination sites in 1, forming a mesh-like structure. Crystal structure analysis and theoretical calculations indicate that the conformation of 1 was controlled by the formation of metal coordination bonds and intramolecular hydrogen bonds. Because of the structural flexibility, the cyclic framework formed both circular and ellipsoidal structures in the crystalline state, depending on the packing structure. In addition, by the conditions of the assembly process, the size of the cavities could be tuned either with a small decrement (dodecanuclear complex [1<sub>12</sub>Ni<sub>12</sub>]<sup>24+</sup>) or a large decrement (octanuclear complexes [(1-3H<sup>+</sup>)<sub>4</sub>Ni<sub>8</sub>]<sup>4+</sup>), in which "shrunk" cavities with a 10-fold difference in diameter (&lt;0.2 nm) were formed by tuning the tripeptide conformation through additional metal coordination to the tripeptide framework. Dynamic light scattering and mass spectrometry studies indicated that the giant cyclic complexes were also present in the solution state.

Study Information

Provider

pubmed

Year

2019

Date

2019-05-16T00:00:00.000Z

DOI

10.1021/jacs.9b01541

Citations

20

References

23