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Second-Generation Drosophila Chemical Tags: Sensitivity, Versatility, and Speed

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Peer-reviewed

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Article

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Authors

Sutcliffe, B 
Ng, J 
Auer, TO 
Pasche, M 
Benton, R 

Abstract

Labeling and visualizing cells and subcellular structures within thick tissues, whole organs and even intact animals is key to studying biological processes. This is particularly true for studies of neural circuits where neurons form submicron synapses but have arbors that may span millimeters in length. Traditionally, labeling is achieved by immunofluorescence; however diffusion of antibody molecules (>100 kDa) is slow and often results in uneven labeling with very poor penetration into the centre of thick specimens; these limitations can be partially addressed by extending staining protocols to over a week (Drosophila brain) and months (mice). Recently we developed an alternative approach using genetically encoded chemical tags CLIP, SNAP, Halo and TMP for tissue labeling; this resulted in >100 fold increase in labeling speed in both mice and Drosophila, at the expense of a considerable drop in absolute sensitivity when compared to optimized immunofluorescence staining. We now present a second generation of UAS and LexA responsive CLIPf, SNAPf and Halo chemical labeling reagents for flies. These multimerized tags, with translational enhancers, display up to 64 fold increase in sensitivity over first generation reagents. In addition we developed a suite of conditional reporters (4xSNAPf tag and CLIPf-SNAPf-Halo2) that are activated by the DNA recombinase Bxb1. Our new reporters can be used with weak and strong GAL4 and LexA drivers and enable stochastic, intersectional and multicolor Brainbow labeling. These improvements in sensitivity and experimental versatility, while still retaining the substantial speed advantage that is a signature of chemical labeling, should significantly increase the scope of this technology.

Description

Keywords

chemical labeling, chemical tags, fluorescence microscopy, immunohistochemistry, neural circuits, protein labeling, Alkyl and Aryl Transferases, Animals, Brain, Drosophila, Drosophila Proteins, Fluorescent Dyes, Microscopy, Fluorescence, Optical Imaging, Recombinant Proteins, Sensitivity and Specificity, Staining and Labeling

Journal Title

Genetics

Conference Name

Journal ISSN

0016-6731
1943-2631

Volume Title

205

Publisher

Genetics Society of America
Sponsorship
European Research Council (649111)
This work was supported by the Medical Research Council (MRC file reference U105188491 and U105178788), European Research Council Starting Investigator (211089) and Consolidator grants (649111) to G.S.X.E.J., and a Royal Society Dorothy Hodgkin Fellowship to S.C. T.O.A. is supported by a Human Frontier Science Program Long Term Fellowship. Research in R.B.’s laboratory is supported by the University of Lausanne and an ERC Consolidator grant (615094). Stocks obtained from the Bloomington Drosophila Stock Center (NIH P40OD018537) were used in this study.
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