Document Type

Article

Language

eng

Format of Original

5 p.

Publication Date

3-2016

Publisher

Springer Verlag

Source Publication

Journal of Fluorescence

Source ISSN

1053-0509

Original Item ID

doi: 10.1007/s10895-015-1743-6; PubMed Central, PMID: 26662810

Abstract

Supported phospholipid bilayers are a convenient model of cellular membranes in studies of membrane biophysics and protein-lipid interactions. Traditionally, supported lipid bilayers are formed on a flat surface of a glass slide to be observed through fluorescence microscopes. This paper describes a method to enable fluorescence detection from the supported lipid bilayers using standard horizontal-beam spectrofluorometers instead of the microscopes. In the proposed approach, the supported lipid bilayers are formed on the inner optical surfaces of the standard fluorescence microcell. To enable observation of the bilayer absorbed on the cell wall, the microcell is placed in a standard fluorometer cell holder and specifically oriented to expose the inner cell walls to both excitation and emission channels with a help of the custom cell adaptor. The signal intensity from supported bilayers doped with 1 % (mol) of rhodamine-labeled lipid in the standard 3-mm optical microcell was equivalent to fluorescence of the 70–80 nM reference solution of rhodamine recorded in a commercial microcell adaptor. Because no modifications to the instruments are required in this method, a variety of steady-state and time-domain fluorescence measurements of the supported phospholipid bilayers may be performed with the spectral resolution using standard horizontal-beam spectrofluorometers.

Comments

Accepted version. Journal of Fluorescence, Vol. 26, No. 2 (March 2016): 379-383. DOI. © 2015 Springer Science+Business Media New York. Used with permission.

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