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Dihexa

N-(1-Oxohexyl)-L-tyrosyl-N-(6-amino-6-oxohexyl)-L-isoleucinamide, N-hexanoic-Tyr-Ile-(6) aminohexanoic amide, PNB-0408

Quick Stats
Studies 17
Trials 0
2014 pubmed 2 citations

Phase segregation of polymerizable lipids to construct filters for separating lipid-membrane-embedded species.

Hu. Shu-Kai SK; Chen. Ya-Ming YM; Chao. Ling L

Key Findings

  • Phase‑segregated mixtures of a polymerizable lipid (DiynePC) and a non‑polymerizable lipid (DOPC) can be UV‑crosslinked to create fixed filter structures in supported lipid bilayers.
  • Adjusting the DiynePC/DOPC ratio changes the filter’s cutoff size, allowing selective passage of smaller versus larger membrane‑embedded molecules.
  • The technique was demonstrated using two model species, showing that higher DiynePC content (80/20) blocks both small and large molecules.

Practical Outcomes

  • For biohackers or DIY researchers, this paper offers a new way to build nanoscale membrane filters, but it provides no direct guidance on using or improving the peptide dihexa, nor any health‑related protocols.

Summary

The study describes a lab technique for making tiny filters in artificial cell membranes using special lipids that can be hardened with UV light. It shows how changing the mix of two lipids changes the size of openings that let different membrane‑bound molecules pass. The work is purely methodological and does not involve the peptide dihexa or any health‑related application.

Abstract

Supported lipid bilayer (SLB) platforms have been developed to transport and separate membrane-embedded species in the species' native bilayer environment. In this study, we used the phase segregation phenomenon of lipid mixtures containing a polymerizable diacetylene phospholipid, 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (DiynePC), and a nonpolymerizable phospholipid, 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), to create filter barrier structures in SLBs. Upon exposing the phase segregated samples to UV light, the DiynePC-rich domains could become crosslinked and remain fixed on the surface of the support, while the DOPC-rich regions, where no crosslinking could happen, could be removed later by detergent washing, and thus became the void regions in the filter. During the filter fabrication process, we used the laminar flow configuration in a microfluidic channel to control the spatial locations of the feed region and filter region in the SLB. The flow in a microfluidic channel was also used to apply a strong hydrodynamic shear stress to the SLB to transport the membrane-embedded species from the feed region to the filter region. We varied the DiynePC/DOPC molar ratio from 60/40 to 80/20 to adjust the cutoff size of the filter barriers and used two model membrane-embedded species of different sizes to examine the filtering capability. One of the model species, Texas Red 1,2-dihexa-decanoyl-sn-glycero-3-phosphoethanolamine triethylammonium salt (Texas Red DHPE), had a single-lipid size, and the other species, cholera toxin subunit B-GM1 complex, had a multilipid size. When the DiynePC/DOPC molar ratio was 60/40, both species had high penetration ratios in the filter region. However, when the ratio was increased to 70/30, only the Texas Red DHPE, which was the smaller of the two model species, could penetrate the filter to a considerable extent. When the ratio was increased to 80/20, neither of the model species could penetrate the filter region. The results showed the possibility of using phase segregation of a mixture containing a polymerizable lipid and a nonpolymerizable lipid to fabricate filter barrier structures with tunable cutoff sizes in SLBs.

Study Information

Provider

pubmed

Year

2014

Date

2014-09-12T00:00:00.000Z

DOI

10.1063/1.4895570

Citations

2

References

29