PUBLICATION

Nanoscale Imaging of Caveolin-1 Membrane Domains In Vivo

Authors
Gabor, K.A., Kim, D., Kim, C.H., Hess, S.T.
ID
ZDB-PUB-150204-2
Date
2015
Source
PLoS One   10: e0117225 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Animals
  • Caveolin 1/chemistry*
  • Caveolin 1/metabolism
  • Cell Membrane/metabolism*
  • Microscopy, Fluorescence/methods*
  • Nanotechnology/methods*
  • Protein Structure, Tertiary
  • Protein Transport
  • Zebrafish
PubMed
25646724 Full text @ PLoS One
Abstract
Light microscopy enables noninvasive imaging of fluorescent species in biological specimens, but resolution is generally limited by diffraction to ~200-250 nm. Many biological processes occur on smaller length scales, highlighting the importance of techniques that can image below the diffraction limit and provide valuable single-molecule information. In recent years, imaging techniques have been developed which can achieve resolution below the diffraction limit. Utilizing one such technique, fluorescence photoactivation localization microscopy (FPALM), we demonstrated its ability to construct super-resolution images from single molecules in a living zebrafish embryo, expanding the realm of previous super-resolution imaging to a living vertebrate organism. We imaged caveolin-1 in vivo, in living zebrafish embryos. Our results demonstrate the successful image acquisition of super-resolution images in a living vertebrate organism, opening several opportunities to answer more dynamic biological questions in vivo at the previously inaccessible nanoscale.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping