Active focus stabilization for upright selective plane illumination microscopy

被引:11
作者
Hedde, Per Niklas [1 ]
Gratton, Enrico [1 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Fluorescence Dynam Lab, Irvine, CA 92697 USA
来源
OPTICS EXPRESS | 2015年 / 23卷 / 11期
基金
美国国家卫生研究院;
关键词
LIGHT-SHEET MICROSCOPY; LIVING CELLS; BEAM;
D O I
10.1364/OE.23.014707
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Due to its sectioning capability, large field of view, and minimal light exposure, selective plane illumination microscopy has become the preferred choice for 3D time lapse imaging. Single cells in a dish can be conveniently imaged using an upright/inverted configuration. However, for measurements on long time scales (hours to days), mechanical drift is a problem; especially for studies of mammalian cells that typically require heating to 37 degrees C which causes a thermal gradient across the instrument. Since the light sheet diverges towards the edges of the field of view, such a drift leads to a decrease in axial resolution over time. Or, even worse, the specimen could move out of the imaging volume. Here, we present a simple, cost-effective way to stabilize the axial position using the microscope camera to track the sample position. Thereby, sample loss is prevented and an optimal axial resolution is maintained by keeping the sample at the position where the light sheet is at its thinnest. We demonstrate the virtue of our approach by measurements of the light sheet thickness and 3D time lapse imaging of a cell monolayer at physiological conditions. (C) 2015 Optical Society of America
引用
收藏
页码:14707 / 14714
页数:8
相关论文
共 13 条
  • [1] Scanned light sheet microscopy with confocal slit detection
    Baumgart, Eugen
    Kubitscheck, Ulrich
    [J]. OPTICS EXPRESS, 2012, 20 (19): : 21805 - 21814
  • [2] Paxillin comes of age
    Deakin, Nicholas O.
    Turner, Christopher E.
    [J]. JOURNAL OF CELL SCIENCE, 2008, 121 (15) : 2435 - 2444
  • [3] Mapping the number of molecules and brightness in the laser scanning microscope
    Digman, Michelle A.
    Dalal, Rooshin
    Horwitz, Alan F.
    Gratton, Enrico
    [J]. BIOPHYSICAL JOURNAL, 2008, 94 (06) : 2320 - 2332
  • [4] Detecting Protein Complexes in Living Cells from Laser Scanning Confocal Image Sequences by the Cross Correlation Raster Image Spectroscopy Method
    Digman, Michelle A.
    Wiseman, Paul W.
    Horwitz, Alan R.
    Gratton, Enrico
    [J]. BIOPHYSICAL JOURNAL, 2009, 96 (02) : 707 - 716
  • [5] Edelstein Arthur D, 2014, J Biol Methods, V1
  • [6] STED-SPIM: Stimulated Emission Depletion Improves Sheet Illumination Microscopy Resolution
    Friedrich, Mike
    Gan, Qiang
    Ermolayev, Vladimir
    Harms, Gregory S.
    [J]. BIOPHYSICAL JOURNAL, 2011, 100 (08) : L43 - L45
  • [7] Extend the field of view of selective plan illumination microscopy by tiling the excitation light sheet
    Gao, Liang
    [J]. OPTICS EXPRESS, 2015, 23 (05): : 6102 - 6111
  • [8] Rapid Measurement of Molecular Transport and Interaction inside Living Cells Using Single Plane Illumination
    Hedde, Per Niklas
    Stakic, Milka
    Gratton, Enrico
    [J]. SCIENTIFIC REPORTS, 2014, 4
  • [9] Optical sectioning deep inside live embryos by selective plane illumination microscopy
    Huisken, J
    Swoger, J
    Del Bene, F
    Wittbrodt, J
    Stelzer, EHK
    [J]. SCIENCE, 2004, 305 (5686) : 1007 - 1009
  • [10] Krzic U, 2012, NAT METHODS, V9, P730, DOI [10.1038/nmeth.2064, 10.1038/NMETH.2064]