Abstract

The surface pressure and surface potential of a two-dimensional solution of prostaglandin E 1 and its synthetic analog E 1α have been investigated using mixed monolayers in a phosphatidylcholine matrix. The properties of the monolayers, most notably their compressibility, were compared with the proton and glucose permeability of bilayer liposomes containing the same prostaglandins. It was found that the presence of the synthetic prostaglandin in the phospatidylcholine membrane caused a five-fold increase in the proton permeability. This effect is explained in terms of the formation of small two-dimensional domains of prostaglandins. Glucose permeability, however, decreased by two orders of magnitude when synthetic prostaglandin was added to the phosphatidylcholine membrane, possibly because of a decrease in the lateral compressibility of the membrane. Possible causes of this phenomenon are discussed in terms of a dynamic pore model.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.