Saturation modified point spread functions in two-photon microscopy
Excitation saturation can dramatically alter the effective imaging point spread function (PSF) in two‐photon fluorescence microscopy. The saturation‐modified PSF can have important implications for resolution in fluorescence imaging as saturation leads to both an increased fluorescence observation v...
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Veröffentlicht in: | Microscopy research and technique 2004-06, Vol.64 (2), p.135-141 |
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creator | Cianci, Gianguido C. Wu, Jianrong Berland, Keith M. |
description | Excitation saturation can dramatically alter the effective imaging point spread function (PSF) in two‐photon fluorescence microscopy. The saturation‐modified PSF can have important implications for resolution in fluorescence imaging as saturation leads to both an increased fluorescence observation volume and an altered spatial profile for the PSF. We introduce here a computational approach to accurately quantify molecular excitation profiles that represent the modified imaging PSF in two‐photon microscopy under the influence of excitation saturation. An analytical model that accounts for pulsed laser excitation is developed to calculate the influence of saturation at any location within the excitation laser profile. The overall saturation modified molecular excitation profiles are then evaluated numerically. Our results demonstrate that saturation can play an important role in two‐photon fluorescence microscopy even with relatively modest excitation levels. Microsc. Res. Tech. 64:135–141, 2004. © 2004 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jemt.20071 |
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Tech. 64:135–141, 2004. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 1059-910X</identifier><identifier>EISSN: 1097-0029</identifier><identifier>DOI: 10.1002/jemt.20071</identifier><identifier>PMID: 15352084</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>fluorescence correlation spectroscopy ; fluorescence microscopy ; Fluorescent Dyes ; Image Interpretation, Computer-Assisted - instrumentation ; Image Interpretation, Computer-Assisted - methods ; Microscopy, Fluorescence, Multiphoton - instrumentation ; Microscopy, Fluorescence, Multiphoton - methods ; Models, Biological ; saturation ; Spectrometry, Fluorescence - instrumentation ; Spectrometry, Fluorescence - methods</subject><ispartof>Microscopy research and technique, 2004-06, Vol.64 (2), p.135-141</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>Copyright 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4601-38c816e72c5f8bfcd954a7f8fa29341879c6099ff7c85209db3bb5ee6605e6923</citedby><cites>FETCH-LOGICAL-c4601-38c816e72c5f8bfcd954a7f8fa29341879c6099ff7c85209db3bb5ee6605e6923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjemt.20071$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjemt.20071$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15352084$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cianci, Gianguido C.</creatorcontrib><creatorcontrib>Wu, Jianrong</creatorcontrib><creatorcontrib>Berland, Keith M.</creatorcontrib><title>Saturation modified point spread functions in two-photon microscopy</title><title>Microscopy research and technique</title><addtitle>Microsc. Res. Tech</addtitle><description>Excitation saturation can dramatically alter the effective imaging point spread function (PSF) in two‐photon fluorescence microscopy. The saturation‐modified PSF can have important implications for resolution in fluorescence imaging as saturation leads to both an increased fluorescence observation volume and an altered spatial profile for the PSF. We introduce here a computational approach to accurately quantify molecular excitation profiles that represent the modified imaging PSF in two‐photon microscopy under the influence of excitation saturation. An analytical model that accounts for pulsed laser excitation is developed to calculate the influence of saturation at any location within the excitation laser profile. The overall saturation modified molecular excitation profiles are then evaluated numerically. Our results demonstrate that saturation can play an important role in two‐photon fluorescence microscopy even with relatively modest excitation levels. Microsc. Res. 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Res. Tech</addtitle><date>2004-06-01</date><risdate>2004</risdate><volume>64</volume><issue>2</issue><spage>135</spage><epage>141</epage><pages>135-141</pages><issn>1059-910X</issn><eissn>1097-0029</eissn><abstract>Excitation saturation can dramatically alter the effective imaging point spread function (PSF) in two‐photon fluorescence microscopy. The saturation‐modified PSF can have important implications for resolution in fluorescence imaging as saturation leads to both an increased fluorescence observation volume and an altered spatial profile for the PSF. We introduce here a computational approach to accurately quantify molecular excitation profiles that represent the modified imaging PSF in two‐photon microscopy under the influence of excitation saturation. An analytical model that accounts for pulsed laser excitation is developed to calculate the influence of saturation at any location within the excitation laser profile. 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subjects | fluorescence correlation spectroscopy fluorescence microscopy Fluorescent Dyes Image Interpretation, Computer-Assisted - instrumentation Image Interpretation, Computer-Assisted - methods Microscopy, Fluorescence, Multiphoton - instrumentation Microscopy, Fluorescence, Multiphoton - methods Models, Biological saturation Spectrometry, Fluorescence - instrumentation Spectrometry, Fluorescence - methods |
title | Saturation modified point spread functions in two-photon microscopy |
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