Ultrafast tissue staining with chemical tags

被引:48
作者
Kohl, Johannes [1 ]
Ng, Julian [1 ]
Cachero, Sebastian [1 ]
Ciabatti, Ernesto [1 ]
Dolan, Michael-John [1 ]
Sutcliffe, Ben [1 ]
Tozer, Adam [1 ]
Ruehle, Sabine [1 ]
Krueger, Daniel [1 ]
Frechter, Shahar [1 ]
Branco, Tiago [1 ]
Tripodi, Marco [1 ]
Jefferis, Gregory S. X. E. [1 ]
机构
[1] Div Neurobiol, Med Res Council Lab Mol Biol, Cambridge CB2 0QH, England
基金
欧洲研究理事会; 英国医学研究理事会; 英国惠康基金;
关键词
immunohistochemistry; neural circuits; protein labeling; fluorescence microscopy; GREEN FLUORESCENT PROTEIN; TARGETED GENE-EXPRESSION; DROSOPHILA-MELANOGASTER; NEURAL CIRCUIT; LIVING CELLS; IN-VIVO; BRAIN; RECONSTRUCTION; DNA; INTERNEURONS;
D O I
10.1073/pnas.1411087111
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
Genetically encoded fluorescent proteins and immunostaining are widely used to detect cellular and subcellular structures in fixed biological samples. However, for thick or whole-mount tissue, each approach suffers from limitations, including limited spectral flexibility and lower signal or slow speed, poor penetration, and high background labeling, respectively. We have overcome these limitations by using transgenically expressed chemical tags for rapid, even, high-signal and low-background labeling of thick biological tissues. We first construct a platform of widely applicable transgenic Drosophila reporter lines, demonstrating that chemical labeling can accelerate staining of whole-mount fly brains by a factor of 100. Using viral vectors to deliver chemical tags into the mouse brain, we then demonstrate that this labeling strategy works well in mice. Thus this tag-based approach drastically improves the speed and specificity of labeling genetically marked cells in intact and/or thick biological samples.
引用
收藏
页码:E3805 / E3814
页数:10
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