Cargando…

Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy

We demonstrate a fiber-based, three-color femtosecond source for simultaneous imaging of three fluorescent proteins (FPs) using two-photon fluorescence microscopy (2PM). The three excitation wavelengths at 775 nm, 864 nm and 950 nm, are obtained through second harmonic generation (SHG) of the 1550-n...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Ke, Liu, Tzu-Ming, Wu, Juwell, Horton, Nicholas G., Lin, Charles P., Xu, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447541/
https://www.ncbi.nlm.nih.gov/pubmed/23024893
http://dx.doi.org/10.1364/BOE.3.001972
_version_ 1782244107777736704
author Wang, Ke
Liu, Tzu-Ming
Wu, Juwell
Horton, Nicholas G.
Lin, Charles P.
Xu, Chris
author_facet Wang, Ke
Liu, Tzu-Ming
Wu, Juwell
Horton, Nicholas G.
Lin, Charles P.
Xu, Chris
author_sort Wang, Ke
collection PubMed
description We demonstrate a fiber-based, three-color femtosecond source for simultaneous imaging of three fluorescent proteins (FPs) using two-photon fluorescence microscopy (2PM). The three excitation wavelengths at 775 nm, 864 nm and 950 nm, are obtained through second harmonic generation (SHG) of the 1550-nm pump laser and the 1728-nm and 1900-nm solitons generated through soliton self-frequency shift (SSFS) in a large-mode-area (LMA) fiber. These energetic pulses are well matched to the two-photon excitation peaks of red, cyan and yellow fluorescent proteins (TagRFPs, TagCFPs, and TagYFPs) for efficient excitation. We demonstrate simultaneous 2PM of human melanoma cells expressing a “rainbow” combination of these three fluorescent proteins.
format Online
Article
Text
id pubmed-3447541
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Optical Society of America
record_format MEDLINE/PubMed
spelling pubmed-34475412012-09-28 Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy Wang, Ke Liu, Tzu-Ming Wu, Juwell Horton, Nicholas G. Lin, Charles P. Xu, Chris Biomed Opt Express Microscopy We demonstrate a fiber-based, three-color femtosecond source for simultaneous imaging of three fluorescent proteins (FPs) using two-photon fluorescence microscopy (2PM). The three excitation wavelengths at 775 nm, 864 nm and 950 nm, are obtained through second harmonic generation (SHG) of the 1550-nm pump laser and the 1728-nm and 1900-nm solitons generated through soliton self-frequency shift (SSFS) in a large-mode-area (LMA) fiber. These energetic pulses are well matched to the two-photon excitation peaks of red, cyan and yellow fluorescent proteins (TagRFPs, TagCFPs, and TagYFPs) for efficient excitation. We demonstrate simultaneous 2PM of human melanoma cells expressing a “rainbow” combination of these three fluorescent proteins. Optical Society of America 2012-07-31 /pmc/articles/PMC3447541/ /pubmed/23024893 http://dx.doi.org/10.1364/BOE.3.001972 Text en ©2012 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.
spellingShingle Microscopy
Wang, Ke
Liu, Tzu-Ming
Wu, Juwell
Horton, Nicholas G.
Lin, Charles P.
Xu, Chris
Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy
title Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy
title_full Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy
title_fullStr Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy
title_full_unstemmed Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy
title_short Three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy
title_sort three-color femtosecond source for simultaneous excitation of three fluorescent proteins in two-photon fluorescence microscopy
topic Microscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447541/
https://www.ncbi.nlm.nih.gov/pubmed/23024893
http://dx.doi.org/10.1364/BOE.3.001972
work_keys_str_mv AT wangke threecolorfemtosecondsourceforsimultaneousexcitationofthreefluorescentproteinsintwophotonfluorescencemicroscopy
AT liutzuming threecolorfemtosecondsourceforsimultaneousexcitationofthreefluorescentproteinsintwophotonfluorescencemicroscopy
AT wujuwell threecolorfemtosecondsourceforsimultaneousexcitationofthreefluorescentproteinsintwophotonfluorescencemicroscopy
AT hortonnicholasg threecolorfemtosecondsourceforsimultaneousexcitationofthreefluorescentproteinsintwophotonfluorescencemicroscopy
AT lincharlesp threecolorfemtosecondsourceforsimultaneousexcitationofthreefluorescentproteinsintwophotonfluorescencemicroscopy
AT xuchris threecolorfemtosecondsourceforsimultaneousexcitationofthreefluorescentproteinsintwophotonfluorescencemicroscopy