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Article
Translocation of Hydrophilic Molecules across Lipid Bilayers by Salt-Bridged Oligocholates
Langmuir
  • Hongkwan Cho, Iowa State University
  • Yan Zhao, Iowa State University
Document Type
Article
Disciplines
Publication Version
Published Version
Publication Date
3-1-2011
DOI
10.1021/la2005166
Abstract
Macrocyclic oligocholates were found in a previous work (Cho, H.; Widanapathirana, L.; Zhao, Y. J. Am. Chem. Soc.2011, 133, 141−147) to stack on top of one another in lipid membranes to form nanopores. Pore formation was driven by a strong tendency of the water molecules in the interior of the amphiphilic macrocycles to aggregate in a nonpolar environment. In this work, cholate oligomers terminated with guanidinium and carboxylate groups were found to cause efflux of hydrophilic molecules such as glucose, maltotriose, and carboxyfluorescein (CF) from POPC/POPG liposomes. The cholate trimer outperformed other oligomers in the transport. Lipid-mixing assays and dynamic light scattering ruled out fusion as the cause of leakage. The strong dependence on chain length argues against random intermolecular aggregates as the active transporters. The efflux of glucose triggered by these compounds increased significantly when the bilayers contained 30 mol % cholesterol. Hill analysis suggested that the active transporter consisted of four molecules. The oligocholates were proposed to fold into “noncovalent macrocycles” by the guanidinium−carboxylate salt bridge and stack on top of one another to form similar transmembrane pores as their covalent counterparts.
Comments

Reprinted (adapted) with permission from Langmuir 27 (2011): 4936, doi:10.1021/la2005166. Copyright 2011 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
File Format
application/pdf
Citation Information
Hongkwan Cho and Yan Zhao. "Translocation of Hydrophilic Molecules across Lipid Bilayers by Salt-Bridged Oligocholates" Langmuir Vol. 27 Iss. 8 (2011) p. 4936 - 4944
Available at: http://works.bepress.com/yan_zhao/29/