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Article: Mid-infrared metabolic imaging with vibrational probes

TitleMid-infrared metabolic imaging with vibrational probes
Authors
Issue Date2020
PublisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/nmeth
Citation
Nature Methods, 2020, v. 17, p. 844-851 How to Cite?
AbstractUnderstanding metabolism is indispensable in unraveling the mechanistic basis of many physiological and pathological processes. However, in situ metabolic imaging tools are still lacking. Here we introduce a framework for mid-infrared (MIR) metabolic imaging by coupling the emerging high-information-throughput MIR microscopy with specifically designed IR-active vibrational probes. We present three categories of small vibrational tags including azide bond, 13C-edited carbonyl bond and deuterium-labeled probes to interrogate various metabolic activities in cells, small organisms and mice. Two MIR imaging platforms are implemented including broadband Fourier transform infrared microscopy and discrete frequency infrared microscopy with a newly incorporated spectral region (2,000–2,300 cm−1). Our technique is uniquely suited to metabolic imaging with high information throughput. In particular, we performed single-cell metabolic profiling including heterogeneity characterization, and large-area metabolic imaging at tissue or organ level with rich spectral information.
Persistent Identifierhttp://hdl.handle.net/10722/284996
ISSN
2021 Impact Factor: 47.990
2020 SCImago Journal Rankings: 19.469
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorShi, L-
dc.contributor.authorLiu, X-
dc.contributor.authorShi, L-
dc.contributor.authorStinson, HT-
dc.contributor.authorRowlette, J-
dc.contributor.authorKahl, LJ-
dc.contributor.authorEvans, CR-
dc.contributor.authorZheng, C-
dc.contributor.authorDietrich, LEP-
dc.contributor.authorMin, W-
dc.date.accessioned2020-08-07T09:05:23Z-
dc.date.available2020-08-07T09:05:23Z-
dc.date.issued2020-
dc.identifier.citationNature Methods, 2020, v. 17, p. 844-851-
dc.identifier.issn1548-7091-
dc.identifier.urihttp://hdl.handle.net/10722/284996-
dc.description.abstractUnderstanding metabolism is indispensable in unraveling the mechanistic basis of many physiological and pathological processes. However, in situ metabolic imaging tools are still lacking. Here we introduce a framework for mid-infrared (MIR) metabolic imaging by coupling the emerging high-information-throughput MIR microscopy with specifically designed IR-active vibrational probes. We present three categories of small vibrational tags including azide bond, 13C-edited carbonyl bond and deuterium-labeled probes to interrogate various metabolic activities in cells, small organisms and mice. Two MIR imaging platforms are implemented including broadband Fourier transform infrared microscopy and discrete frequency infrared microscopy with a newly incorporated spectral region (2,000–2,300 cm−1). Our technique is uniquely suited to metabolic imaging with high information throughput. In particular, we performed single-cell metabolic profiling including heterogeneity characterization, and large-area metabolic imaging at tissue or organ level with rich spectral information.-
dc.languageeng-
dc.publisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/nmeth-
dc.relation.ispartofNature Methods-
dc.rightsThis is a post-peer-review, pre-copyedit version of an article published in [insert journal title]. The final authenticated version is available online at: https://doi.org/[insert DOI]-
dc.titleMid-infrared metabolic imaging with vibrational probes-
dc.typeArticle-
dc.identifier.emailZheng, C: cgzheng@hku.hk-
dc.identifier.authorityZheng, C=rp02473-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41592-020-0883-z-
dc.identifier.pmid32601425-
dc.identifier.pmcidPMC7396315-
dc.identifier.scopuseid_2-s2.0-85087009316-
dc.identifier.hkuros312513-
dc.identifier.volume17-
dc.identifier.spage844-
dc.identifier.epage851-
dc.identifier.isiWOS:000544223800004-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl1548-7091-

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