High refractive index substrates for fluorescence microscopy of biological interfaces with high z contrast

被引:27
作者
Ajo-Franklin, CM [1 ]
Kam, L [1 ]
Boxer, SG [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1073/pnas.241208698
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Total internal reflection fluorescence microscopy is widely used to confine the excitation of a complex fluorescent sample very close to the material on which it is supported. By working with high refractive index solid supports, it is possible to confine even further the evanescent field, and by varying the angle of incidence, to obtain quantitative information on the distance of the fluorescent object from the surface. We report the fabrication of hybrid surfaces consisting of nm layers Of SiO2 on lithium niobate (LiNbO3 n = 2.3). Supported lipid bilayer membranes can be assembled and patterned on these hybrid surfaces as on conventional glass. By varying the angle of incidence of the excitation light, we are able to obtain fluorescent contrast between 40-nm fluorescent beads tethered to a supported bilayer and fluorescently labeled protein printed on the surface, which differ in vertical position by only tens of nm. Preliminary experiments that test theoretical models for the fluorescence-collection factor near a high refractive index surface are presented, and this factor is incorporated into a semiquantitative model used to predict the contrast of the 40-nm bead/protein system. These results demonstrate that it should be possible to profile the vertical location of fluorophores on the nm distance scale in real time, opening the possibility of many experiments at the interface between supported membranes and living cells. improvements in materials and optical techniques are outlined.
引用
收藏
页码:13643 / 13648
页数:6
相关论文
共 35 条
[1]  
Axelrod D, 1991, TOPICS FLUORESCENCE, V3, P289
[2]   4Pi-confocal microscopy of live cells [J].
Bahlmann, K ;
Jakobs, S ;
Hell, SW .
ULTRAMICROSCOPY, 2001, 87 (03) :155-164
[3]   PHYSICAL-PROPERTIES OF SINGLE PHOSPHOLIPID-BILAYERS ADSORBED TO MICRO GLASS-BEADS - A NEW VESICULAR MODEL SYSTEM STUDIED BY H-2-NUCLEAR MAGNETIC-RESONANCE [J].
BAYERL, TM ;
BLOOM, M .
BIOPHYSICAL JOURNAL, 1990, 58 (02) :357-362
[4]   Molecular transport and organization in supported lipid membranes [J].
Boxer, SG .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2000, 4 (06) :704-709
[5]   Fluorescence interferometry of neuronal cell adhesion on microstructured silicon [J].
Braun, D ;
Fromherz, P .
PHYSICAL REVIEW LETTERS, 1998, 81 (23) :5241-5244
[6]   ALLOGENEIC STIMULATION OF CYTO-TOXIC T-CELLS BY SUPPORTED PLANAR MEMBRANES [J].
BRIAN, AA ;
MCCONNELL, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (19) :6159-6163
[7]   EFFECT OF PLANAR DIELECTRIC INTERFACES ON FLUORESCENCE EMISSION AND DETECTION - EVANESCENT EXCITATION WITH HIGH-APERTURE COLLECTION [J].
BURGHARDT, TP ;
THOMPSON, NL .
BIOPHYSICAL JOURNAL, 1984, 46 (06) :729-737
[8]   QUANTITATIVE-ANALYSIS OF VARIABLE-ANGLE TOTAL INTERNAL-REFLECTION FLUORESCENCE MICROSCOPY (VA-TIRFM) OF CELL SUBSTRATE CONTACTS [J].
BURMEISTER, JS ;
TRUSKEY, GA ;
REICHERT, WM .
JOURNAL OF MICROSCOPY-OXFORD, 1994, 173 :39-51
[9]   SUPERRESOLUTION 3-DIMENSIONAL IMAGES OF FLUORESCENCE IN CELLS WITH MINIMAL LIGHT EXPOSURE [J].
CARRINGTON, WA ;
LYNCH, RM ;
MOORE, EDW ;
ISENBERG, G ;
FOGARTY, KE ;
FREDRIC, FS .
SCIENCE, 1995, 268 (5216) :1483-1487
[10]   Lateral resolution enhancement with standing evanescent waves [J].
Cragg, GE ;
So, PTC .
OPTICS LETTERS, 2000, 25 (01) :46-48