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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Microscopy research and technique 2004-06, Vol.64 (2), p.135-141
Hauptverfasser: Cianci, Gianguido C., Wu, Jianrong, Berland, Keith M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 141
container_issue 2
container_start_page 135
container_title Microscopy research and technique
container_volume 64
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_66849037</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>66849037</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4601-38c816e72c5f8bfcd954a7f8fa29341879c6099ff7c85209db3bb5ee6605e6923</originalsourceid><addsrcrecordid>eNqFkDFPwzAQhS0EoqWw8ANQJgakFDuO7XhEVSlUBVRRKJvlOLZwaeIQJyr99zS0wAbTne6-93T3ADhFsI8gjC4XOq_7EYQM7YEugpyFmynfb3vCQ47gSwcceb-AECGC4kPQQQSTCCZxFwweZd1UsrauCHKXWWN1FpTOFnXgy0rLLDBNodq1D2wR1CsXlq-ubmmrKueVK9fH4MDIpdcnu9oDT9fD2eAmnDyMbgdXk1DFFKIQJypBVLNIEZOkRmWcxJKZxMiI4xgljCsKOTeGqWRzHc9SnKZEa0oh0ZRHuAfOt75l5d4b7WuRW6_0cikL7RovKE1iDjH7F0SMRTQiLXixBdtXfKWNKCuby2otEBRttqLNVnxlu4HPdq5NmuvsF92FuQHQFljZpV7_YSXGw7vZt2m41Vhf648fjazeBGWYETG_Hwk-5tNnPJqLKf4Ebx2Thg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17726257</pqid></control><display><type>article</type><title>Saturation modified point spread functions in two-photon microscopy</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Cianci, Gianguido C. ; Wu, Jianrong ; Berland, Keith M.</creator><creatorcontrib>Cianci, Gianguido C. ; Wu, Jianrong ; Berland, Keith M.</creatorcontrib><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.</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. Tech. 64:135–141, 2004. © 2004 Wiley‐Liss, Inc.</description><subject>fluorescence correlation spectroscopy</subject><subject>fluorescence microscopy</subject><subject>Fluorescent Dyes</subject><subject>Image Interpretation, Computer-Assisted - instrumentation</subject><subject>Image Interpretation, Computer-Assisted - methods</subject><subject>Microscopy, Fluorescence, Multiphoton - instrumentation</subject><subject>Microscopy, Fluorescence, Multiphoton - methods</subject><subject>Models, Biological</subject><subject>saturation</subject><subject>Spectrometry, Fluorescence - instrumentation</subject><subject>Spectrometry, Fluorescence - methods</subject><issn>1059-910X</issn><issn>1097-0029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkDFPwzAQhS0EoqWw8ANQJgakFDuO7XhEVSlUBVRRKJvlOLZwaeIQJyr99zS0wAbTne6-93T3ADhFsI8gjC4XOq_7EYQM7YEugpyFmynfb3vCQ47gSwcceb-AECGC4kPQQQSTCCZxFwweZd1UsrauCHKXWWN1FpTOFnXgy0rLLDBNodq1D2wR1CsXlq-ubmmrKueVK9fH4MDIpdcnu9oDT9fD2eAmnDyMbgdXk1DFFKIQJypBVLNIEZOkRmWcxJKZxMiI4xgljCsKOTeGqWRzHc9SnKZEa0oh0ZRHuAfOt75l5d4b7WuRW6_0cikL7RovKE1iDjH7F0SMRTQiLXixBdtXfKWNKCuby2otEBRttqLNVnxlu4HPdq5NmuvsF92FuQHQFljZpV7_YSXGw7vZt2m41Vhf648fjazeBGWYETG_Hwk-5tNnPJqLKf4Ebx2Thg</recordid><startdate>20040601</startdate><enddate>20040601</enddate><creator>Cianci, Gianguido C.</creator><creator>Wu, Jianrong</creator><creator>Berland, Keith M.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20040601</creationdate><title>Saturation modified point spread functions in two-photon microscopy</title><author>Cianci, Gianguido C. ; Wu, Jianrong ; Berland, Keith M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4601-38c816e72c5f8bfcd954a7f8fa29341879c6099ff7c85209db3bb5ee6605e6923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>fluorescence correlation spectroscopy</topic><topic>fluorescence microscopy</topic><topic>Fluorescent Dyes</topic><topic>Image Interpretation, Computer-Assisted - instrumentation</topic><topic>Image Interpretation, Computer-Assisted - methods</topic><topic>Microscopy, Fluorescence, Multiphoton - instrumentation</topic><topic>Microscopy, Fluorescence, Multiphoton - methods</topic><topic>Models, Biological</topic><topic>saturation</topic><topic>Spectrometry, Fluorescence - instrumentation</topic><topic>Spectrometry, Fluorescence - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cianci, Gianguido C.</creatorcontrib><creatorcontrib>Wu, Jianrong</creatorcontrib><creatorcontrib>Berland, Keith M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Microscopy research and technique</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cianci, Gianguido C.</au><au>Wu, Jianrong</au><au>Berland, Keith M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Saturation modified point spread functions in two-photon microscopy</atitle><jtitle>Microscopy research and technique</jtitle><addtitle>Microsc. 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. 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.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15352084</pmid><doi>10.1002/jemt.20071</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1059-910X
ispartof Microscopy research and technique, 2004-06, Vol.64 (2), p.135-141
issn 1059-910X
1097-0029
language eng
recordid cdi_proquest_miscellaneous_66849037
source MEDLINE; Wiley Online Library Journals Frontfile Complete
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T14%3A33%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Saturation%20modified%20point%20spread%20functions%20in%20two-photon%20microscopy&rft.jtitle=Microscopy%20research%20and%20technique&rft.au=Cianci,%20Gianguido%20C.&rft.date=2004-06-01&rft.volume=64&rft.issue=2&rft.spage=135&rft.epage=141&rft.pages=135-141&rft.issn=1059-910X&rft.eissn=1097-0029&rft_id=info:doi/10.1002/jemt.20071&rft_dat=%3Cproquest_cross%3E66849037%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17726257&rft_id=info:pmid/15352084&rfr_iscdi=true