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Two-photon excitation and photoconversion of EosFP in dual-color 4Pi confocal microscopy

Two-photon excitation and photoconversion of EosFP in dual-color 4Pi confocal microscopy
Two-photon excitation and photoconversion of EosFP in dual-color 4Pi confocal microscopy
Recent years have witnessed enormous advances in fluorescence microscopy instrumentation and fluorescent marker development. 4Pi confocal microscopy with two-photon excitation features excellent optical sectioning in the axial direction, with a resolution in the 100 nm range. Here we apply this technique to cellular imaging with EosFP, a photoactivatable autofluorescent protein whose fluorescence emission wavelength can be switched from green (516 nm) to red (581 nm) by irradiation with 400-nm light. We have measured the two-photon excitation spectra and cross sections of the green and the red species as well as the spectral dependence of two-photon conversion. The data reveal that two-photon excitation and photoactivation of the green form of EosFP can be selectively performed by choosing the proper wavelengths. Optical highlighting of small subcellular compartments was shown on HeLa cells expressing EosFP fused to a mitochondrial targeting signal. After three-dimensionally confined two-photon conversion of EosFP within the mitochondrial networks of the cells, the converted regions could be resolved in a 3D reconstruction from a dual-color 4Pi image stack.
0006-3495
4451-4457
Ivanchenko, S.
99165146-f345-45ef-9f34-e72e8af01c41
Glaschick, S.
9eeda3ce-b59c-4c45-8ffd-0ccf99b87486
Röcker, C.
1a2dcd7a-3e54-4663-a32a-50efff9e118d
Oswald, F.
8fea64d4-21b7-4f41-93dd-0c4ce331c84b
Wiedenmann, J.
ad445af2-680f-4927-90b3-589ac9d538f7
Nienhaus, G.U.
8f2b40ea-be57-4b32-880f-8a0e5c1585aa
Ivanchenko, S.
99165146-f345-45ef-9f34-e72e8af01c41
Glaschick, S.
9eeda3ce-b59c-4c45-8ffd-0ccf99b87486
Röcker, C.
1a2dcd7a-3e54-4663-a32a-50efff9e118d
Oswald, F.
8fea64d4-21b7-4f41-93dd-0c4ce331c84b
Wiedenmann, J.
ad445af2-680f-4927-90b3-589ac9d538f7
Nienhaus, G.U.
8f2b40ea-be57-4b32-880f-8a0e5c1585aa

Ivanchenko, S., Glaschick, S., Röcker, C., Oswald, F., Wiedenmann, J. and Nienhaus, G.U. (2007) Two-photon excitation and photoconversion of EosFP in dual-color 4Pi confocal microscopy. Biophysical Journal, 92 (12), 4451-4457. (doi:10.1529/biophysj.106.103408).

Record type: Article

Abstract

Recent years have witnessed enormous advances in fluorescence microscopy instrumentation and fluorescent marker development. 4Pi confocal microscopy with two-photon excitation features excellent optical sectioning in the axial direction, with a resolution in the 100 nm range. Here we apply this technique to cellular imaging with EosFP, a photoactivatable autofluorescent protein whose fluorescence emission wavelength can be switched from green (516 nm) to red (581 nm) by irradiation with 400-nm light. We have measured the two-photon excitation spectra and cross sections of the green and the red species as well as the spectral dependence of two-photon conversion. The data reveal that two-photon excitation and photoactivation of the green form of EosFP can be selectively performed by choosing the proper wavelengths. Optical highlighting of small subcellular compartments was shown on HeLa cells expressing EosFP fused to a mitochondrial targeting signal. After three-dimensionally confined two-photon conversion of EosFP within the mitochondrial networks of the cells, the converted regions could be resolved in a 3D reconstruction from a dual-color 4Pi image stack.

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Published date: 23 March 2007

Identifiers

Local EPrints ID: 51165
URI: http://eprints.soton.ac.uk/id/eprint/51165
ISSN: 0006-3495
PURE UUID: 16fb9396-4c33-41a0-ad0f-fdda76475426
ORCID for J. Wiedenmann: ORCID iD orcid.org/0000-0003-2128-2943

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Date deposited: 08 May 2008
Last modified: 16 Mar 2024 03:53

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Contributors

Author: S. Ivanchenko
Author: S. Glaschick
Author: C. Röcker
Author: F. Oswald
Author: J. Wiedenmann ORCID iD
Author: G.U. Nienhaus

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