Expanding the Range of Bioorthogonal Tags for Multiplex Stimulated Raman Scattering Microscopy
Multiplex optical detection in live cells is challenging due to overlapping signals and poor signal‐to‐noise associated with some chemical reporters. To address this, the application of spectral phasor analysis to stimulated Raman scattering (SRS) microscopy for unmixing three bioorthogonal Raman pr...
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Veröffentlicht in: | Angewandte Chemie 2023-11, Vol.135 (48), p.n/a |
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description | Multiplex optical detection in live cells is challenging due to overlapping signals and poor signal‐to‐noise associated with some chemical reporters. To address this, the application of spectral phasor analysis to stimulated Raman scattering (SRS) microscopy for unmixing three bioorthogonal Raman probes within cells is reported. Triplex detection of a metallacarborane using the B−H stretch at 2480–2650 cm−1, together with a bis‐alkyne and deuterated fatty acid can be achieved within the cell‐silent region of the Raman spectrum. When coupled to imaging in the high‐wavenumber region of the cellular Raman spectrum, nine discrete regions of interest can be spectrally unmixed from the hyperspectral SRS dataset, demonstrating a new capability in the toolkit of multiplexed Raman imaging of live cells.
Hyperspectral stimulated Raman scattering (SRS) microscopy with spectral phasor analysis enables the multiplex detection of bioorthogonal Raman groups in cells. Unmixing of the overlapping alkyne and deuterium signals together with the detection of metallacarboranes is reported within the cell‐silent region of the Raman spectrum. |
doi_str_mv | 10.1002/ange.202311530 |
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Hyperspectral stimulated Raman scattering (SRS) microscopy with spectral phasor analysis enables the multiplex detection of bioorthogonal Raman groups in cells. Unmixing of the overlapping alkyne and deuterium signals together with the detection of metallacarboranes is reported within the cell‐silent region of the Raman spectrum.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.202311530</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Alkynes ; Bioorthogonal Labeling ; Chemistry ; Deuteration ; Imaging Probes ; Microscopy ; Multiplexing ; Phasors ; Raman Microscopy ; Raman spectra ; Raman spectroscopy ; Spectral Phasor Analysis ; Stimulated Raman Scattering ; Wavelengths</subject><ispartof>Angewandte Chemie, 2023-11, Vol.135 (48), p.n/a</ispartof><rights>2023 The Authors. Angewandte Chemie published by Wiley-VCH GmbH</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1570-7a4ef1fcdbf3db8baa8267071ea1cea899751bcf4e872e8532e6623351914ce43</cites><orcidid>0000-0003-4273-2691 ; 0000-0002-6079-2105</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fange.202311530$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fange.202311530$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Murphy, Neville</creatorcontrib><creatorcontrib>Tipping, William J.</creatorcontrib><creatorcontrib>Braddick, Henry J.</creatorcontrib><creatorcontrib>Wilson, Liam T.</creatorcontrib><creatorcontrib>Tomkinson, Nicholas C. O.</creatorcontrib><creatorcontrib>Faulds, Karen</creatorcontrib><creatorcontrib>Graham, Duncan</creatorcontrib><creatorcontrib>Farràs, Pau</creatorcontrib><title>Expanding the Range of Bioorthogonal Tags for Multiplex Stimulated Raman Scattering Microscopy</title><title>Angewandte Chemie</title><description>Multiplex optical detection in live cells is challenging due to overlapping signals and poor signal‐to‐noise associated with some chemical reporters. To address this, the application of spectral phasor analysis to stimulated Raman scattering (SRS) microscopy for unmixing three bioorthogonal Raman probes within cells is reported. Triplex detection of a metallacarborane using the B−H stretch at 2480–2650 cm−1, together with a bis‐alkyne and deuterated fatty acid can be achieved within the cell‐silent region of the Raman spectrum. When coupled to imaging in the high‐wavenumber region of the cellular Raman spectrum, nine discrete regions of interest can be spectrally unmixed from the hyperspectral SRS dataset, demonstrating a new capability in the toolkit of multiplexed Raman imaging of live cells.
Hyperspectral stimulated Raman scattering (SRS) microscopy with spectral phasor analysis enables the multiplex detection of bioorthogonal Raman groups in cells. 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O.</creatorcontrib><creatorcontrib>Faulds, Karen</creatorcontrib><creatorcontrib>Graham, Duncan</creatorcontrib><creatorcontrib>Farràs, Pau</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murphy, Neville</au><au>Tipping, William J.</au><au>Braddick, Henry J.</au><au>Wilson, Liam T.</au><au>Tomkinson, Nicholas C. 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When coupled to imaging in the high‐wavenumber region of the cellular Raman spectrum, nine discrete regions of interest can be spectrally unmixed from the hyperspectral SRS dataset, demonstrating a new capability in the toolkit of multiplexed Raman imaging of live cells.
Hyperspectral stimulated Raman scattering (SRS) microscopy with spectral phasor analysis enables the multiplex detection of bioorthogonal Raman groups in cells. Unmixing of the overlapping alkyne and deuterium signals together with the detection of metallacarboranes is reported within the cell‐silent region of the Raman spectrum.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ange.202311530</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-4273-2691</orcidid><orcidid>https://orcid.org/0000-0002-6079-2105</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alkynes Bioorthogonal Labeling Chemistry Deuteration Imaging Probes Microscopy Multiplexing Phasors Raman Microscopy Raman spectra Raman spectroscopy Spectral Phasor Analysis Stimulated Raman Scattering Wavelengths |
title | Expanding the Range of Bioorthogonal Tags for Multiplex Stimulated Raman Scattering Microscopy |
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