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PMID: 18469823 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Three-dimensional sub-100 nm resolution fluorescence microscopy of thick samples.

Nature methods ·Vol. 5 ·No. 6 ·2008-06-00 ·Pages 527-9

Juette MF, Gould TJ, Lessard MD, Mlodzianoski MJ, Nagpure BS, Bennett BT, Hess ST, Bewersdorf J

Abstract

Imaging volumes as thick as whole cells at three-dimensional (3D) super-resolution is required to reveal unknown features of cellular organization. We report a light microscope that generates images with translationally invariant 30 x 30 x 75 nm resolution over a depth of several micrometers. This method, named biplane (BP) FPALM, combines a double-plane detection scheme with fluorescence photoactivation localization microscopy (FPALM) enabling 3D sub-diffraction resolution without compromising speed or sensitivity.

MeSH Terms
Biophysics/economics,instrumentation,methods Fluorescein/pharmacology Fluorescent Dyes/pharmacology Image Enhancement Image Interpretation, Computer-Assisted/methods Imaging, Three-Dimensional/instrumentation,methods Lasers Light Microscopy/methods Microscopy, Fluorescence/instrumentation,methods Software
Chemicals
Fluorescent Dyes Fluorescein
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Juette Manuel F
Institute for Molecular Biophysics, The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine 04609, USA.
Gould Travis J
Lessard Mark D
Mlodzianoski Michael J
Nagpure Bhupendra S
Bennett Brian T
Hess Samuel T
Bewersdorf Joerg
Article Info
Journal
Nature methods
Abbr.
Nat Methods
ISSN
1548-7105
Published
2008-06-00
Epub
2008-00-11
Pages
527-9
Language
English
Region
United States
NLM ID
101215604
Subset
IM
Grants
NIAID NIH HHS · K25 AI065459 · United States
PHS HHS · K25-65459 · United States
NCI NIH HHS · P30 CA034196 · United States
Corrections
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