Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools

Expanding on their previous work, Bondar et al present open source software tools to reliably quantify linear dichroism and determine molecular orientations. They demonstrate the utility of the tools by imaging synthetic lipid vesicles and as well as fluorescently labelled proteins in living cells

Bibliographic Details
Main Authors: Alexey Bondar, Olga Rybakova, Josef Melcr, Jan Dohnálek, Petro Khoroshyy, Ondřej Ticháček, Štěpán Timr, Paul Miclea, Alina Sakhi, Vendula Marková, Josef Lazar
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-021-01694-1
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spelling doaj-1ddcc28075a347aea94ccfb507f7c9df2021-02-14T12:27:22ZengNature Publishing GroupCommunications Biology2399-36422021-02-014111210.1038/s42003-021-01694-1Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software toolsAlexey Bondar0Olga Rybakova1Josef Melcr2Jan Dohnálek3Petro Khoroshyy4Ondřej Ticháček5Štěpán Timr6Paul Miclea7Alina Sakhi8Vendula Marková9Josef Lazar10Institute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceInstitute of Organic Chemistry and Biochemistry, Czech Academy of ScienceExpanding on their previous work, Bondar et al present open source software tools to reliably quantify linear dichroism and determine molecular orientations. They demonstrate the utility of the tools by imaging synthetic lipid vesicles and as well as fluorescently labelled proteins in living cellshttps://doi.org/10.1038/s42003-021-01694-1
collection DOAJ
language English
format Article
sources DOAJ
author Alexey Bondar
Olga Rybakova
Josef Melcr
Jan Dohnálek
Petro Khoroshyy
Ondřej Ticháček
Štěpán Timr
Paul Miclea
Alina Sakhi
Vendula Marková
Josef Lazar
spellingShingle Alexey Bondar
Olga Rybakova
Josef Melcr
Jan Dohnálek
Petro Khoroshyy
Ondřej Ticháček
Štěpán Timr
Paul Miclea
Alina Sakhi
Vendula Marková
Josef Lazar
Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools
Communications Biology
author_facet Alexey Bondar
Olga Rybakova
Josef Melcr
Jan Dohnálek
Petro Khoroshyy
Ondřej Ticháček
Štěpán Timr
Paul Miclea
Alina Sakhi
Vendula Marková
Josef Lazar
author_sort Alexey Bondar
title Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools
title_short Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools
title_full Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools
title_fullStr Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools
title_full_unstemmed Quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools
title_sort quantitative linear dichroism imaging of molecular processes in living cells made simple by open software tools
publisher Nature Publishing Group
series Communications Biology
issn 2399-3642
publishDate 2021-02-01
description Expanding on their previous work, Bondar et al present open source software tools to reliably quantify linear dichroism and determine molecular orientations. They demonstrate the utility of the tools by imaging synthetic lipid vesicles and as well as fluorescently labelled proteins in living cells
url https://doi.org/10.1038/s42003-021-01694-1
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