PUBLICATION

Precise spatio-temporal control of rapid optogenetic cell ablation with mem-KillerRed in Zebrafish

Authors
Buckley, C., Carvalho, M.T., Young, L.K., Rider, S.A., McFadden, C., Berlage, C., Verdon, R.F., Taylor, J.M., Girkin, J.M., Mullins, J.J.
ID
ZDB-PUB-170713-5
Date
2017
Source
Scientific Reports   7: 5096 (Journal)
Registered Authors
Mullins, John, Rider, Sebastien
Keywords
Fluorescence imaging, Light-sheet microscopy, Optogenetics
MeSH Terms
  • Animals
  • Fluorescence
  • Green Fluorescent Proteins/metabolism
  • Optogenetics/methods*
  • Time Factors
  • Zebrafish/metabolism*
PubMed
28698677 Full text @ Sci. Rep.
Abstract
The ability to kill individual or groups of cells in vivo is important for studying cellular processes and their physiological function. Cell-specific genetically encoded photosensitizing proteins, such as KillerRed, permit spatiotemporal optogenetic ablation with low-power laser light. We report dramatically improved resolution and speed of cell targeting in the zebrafish kidney through the use of a selective plane illumination microscope (SPIM). Furthermore, through the novel incorporation of a Bessel beam into the SPIM imaging arm, we were able to improve on targeting speed and precision. The low diffraction of the Bessel beam coupled with the ability to tightly focus it through a high NA lens allowed precise, rapid targeting of subsets of cells at anatomical depth in live, developing zebrafish kidneys. We demonstrate that these specific targeting strategies significantly increase the speed of optoablation as well as fish survival.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping