In situ imaging of micropatterned phospholipid membranes by surface plasmon fluorescence microscopy

被引:7
|
作者
Tawa, Keiko [1 ]
Morigaki, Kenichi [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, RICE, Osaka 5638577, Japan
关键词
Surface plasmon resonance; Fluorescence microscopy; Imaging; Lipid membrane; Vesicle fusion; LIPID-BILAYERS; SPECTROSCOPY; HYBRIDIZATION; RESONANCE; POLYMERIZATION; MICROARRAYS; PROTEIN;
D O I
10.1016/j.colsurfb.2010.07.038
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A parallel microscopic imaging technique, surface plasmon microscopy (SPM)-surface plasmon fluorescence microscopy (SPFM), is introduced as a versatile analytical tool to monitor biochips. In spite of the fact that the fluorescence excited by surface plasmon is 1-2 order stronger compared with the total internal reflection fluorescence microscopy, SPFM has not fully utilized its advantages because fluorescence from fluorophores near the gold surface is almost entirely quenched due to the Forster energy transfer. In this study, SiO(2) layer sputtered on the gold substrate suppressed the quenching of fluorescence and enabled a parallel measurement of SPM and SPFM. As a model system, micropatterned membranes composed of polymeric and fluid phospholipid bilayers were employed. The difference of film thickness could be detected by SPM, and SPFM provided information on the composition and structure of membranes, enabling the distinction between polymeric and fluid phospholipid bilayers. These results suggest the general applicability of SPM-SPFM for various formats of biochips. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:447 / 451
页数:5
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