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Fluorescently Guided Optical Photothermal Infrared Microspectroscopy for Protein-Specific Bioimaging at Subcellular Level.
Prater, Craig; Bai, Yeran; Konings, Sabine C; Martinsson, Isak; Swaminathan, Vinay S; Nordenfelt, Pontus; Gouras, Gunnar; Borondics, Ferenc; Klementieva, Oxana.
Affiliation
  • Prater C; Photothermal Spectroscopy Corporation, Santa Barbara, California93101, United States.
  • Bai Y; Photothermal Spectroscopy Corporation, Santa Barbara, California93101, United States.
  • Konings SC; Neuroscience Research Institute, University of California, Santa Barbara, Santa Barbara, California93106, United States.
  • Martinsson I; Medical Microspectroscopy, Department of Experimental Medical Science, Lund University, 22180Lund, Sweden.
  • Swaminathan VS; NanoLund, Lund University, 22180Lund, Sweden.
  • Nordenfelt P; Multipark, Lund University, 22180Lund, Sweden.
  • Gouras G; Experimental Dementia Research Group, Department of Experimental Medical Science, Lund University, 22180Lund, Sweden.
  • Borondics F; Multipark, Lund University, 22180Lund, Sweden.
  • Klementieva O; Division of Oncology, Department of Clinical Sciences, Wallenberg Centre for Molecular Medicine (WCMM), Lund University, 22180Lund, Sweden.
J Med Chem ; 66(4): 2542-2549, 2023 02 23.
Article in En | MEDLINE | ID: mdl-36599042
ABSTRACT
Infrared spectroscopic imaging is widely used for the visualization of biomolecule structures, and techniques such as optical photothermal infrared (OPTIR) microspectroscopy can achieve <500 nm spatial resolution. However, these approaches lack specificity for particular cell types and cell components and thus cannot be used as a stand-alone technique to assess their properties. Here, we have developed a novel tool, fluorescently guided optical photothermal infrared microspectroscopy, that simultaneously exploits epifluorescence imaging and OPTIR to perform fluorescently guided IR spectroscopic analysis. This novel approach exceeds the diffraction limit of infrared microscopy and allows structural analysis of specific proteins directly in tissue and single cells. Experiments described herein used epifluorescence to rapidly locate amyloid proteins in tissues or neuronal cultures, thus guiding OPTIR measurements to assess amyloid structures at the subcellular level. We believe that this new approach will be a valuable addition to infrared spectroscopy providing cellular specificity of measurements in complex systems for studies of structurally altered protein aggregates.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amyloidogenic Proteins Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amyloidogenic Proteins Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 2023 Type: Article Affiliation country: United States