Optical super-resolution microscopy in neurobiology

被引:39
|
作者
Sigrist, Stephan J. [1 ]
Sabatini, Bernardo L. [2 ]
机构
[1] Free Univ Berlin, Inst Biol, Berlin, Germany
[2] Harvard Univ, Sch Med, Howard Hughes Med Inst, Dept Neurobiol, Boston, MA 02115 USA
关键词
STED MICROSCOPY; FLUORESCENCE MICROSCOPY; ACTIVE ZONE; RECONSTRUCTION MICROSCOPY; STRUCTURED ILLUMINATION; STIMULATED-EMISSION; RESOLUTION; LOCALIZATION; BRUCHPILOT; DROSOPHILA;
D O I
10.1016/j.conb.2011.10.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Understanding the highly plastic nature of neurons requires the dynamic visualization of their molecular and cellular organization in a native context. However, due to the limited resolution of standard light microscopy, many of the structural specializations of neurons cannot be resolved. A recent revolution in light microscopy has given rise to several super-resolution light microscopy methods yielding 2-10-fold higher resolution than conventional microscopy. We here describe the principles behind these techniques as well as their application to the analysis of the molecular architecture of the synapse. Furthermore, we discuss the potential for continued development of super-resolution microscopy as necessary for live imaging of neuronal structure and function in the brain.
引用
收藏
页码:86 / 93
页数:8
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