In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M

Photoswitchable reagents arc powerful tools for high-precision studies in cell biology. When these reagents are globally administered yet locally photoactivated in two-dimensional (2D) cell cultures, they can exert micron- and millisecond-scale biological control. This gives them great potential for...

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Autores: Gao, Li, Meiring, Joyce C. M., Varady, Adam, Ruider, Iris E., Heise, Constanze, Wranik, Maximilian, Velasco, Cecilia D., Taylor, Jennifer A., Terni, Beatrice, Weinert, Tobias, Standfuss, Jörg, Cabernard, Clemens C., Llobet Berenguer, Artur, 1972-, Steinmetz, Michel O., Bausch, Andreas R., Distel, Martin, Thorn-Seshold, Julia, Akhmanova, Anna, Thorn-Seshold, Oliver
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2022
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/186228
Acceso en línea:https://hdl.handle.net/2445/186228
Access Level:acceso abierto
Palabra clave:Citosquelet
Mitosi
Cytoskeleton
Mitosis
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spelling In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2MGao, LiMeiring, Joyce C. M.Varady, AdamRuider, Iris E.Heise, ConstanzeWranik, MaximilianVelasco, Cecilia D.Taylor, Jennifer A.Terni, BeatriceWeinert, TobiasStandfuss, JörgCabernard, Clemens C.Llobet Berenguer, Artur, 1972-Steinmetz, Michel O.Bausch, Andreas R.Distel, MartinThorn-Seshold, JuliaAkhmanova, AnnaThorn-Seshold, OliverCitosqueletMitosiCytoskeletonMitosisPhotoswitchable reagents arc powerful tools for high-precision studies in cell biology. When these reagents are globally administered yet locally photoactivated in two-dimensional (2D) cell cultures, they can exert micron- and millisecond-scale biological control. This gives them great potential for use in biologically more relevant three-dimensional (3D) models and in vivo, particularly for studying systems with inherent spatiotemporal complexity, such as the cytoskeleton. However, due to a combination of photoswitch isomerization under typical imaging conditions, metabolic liabilities, and insufficient water solubility at effective concentrations, the in vivo potential of photoswitchable reagents addressing cytosolic protein targets remains largely unrealized. Here, we optimized the potency and solubility of metabolically stable, druglike colchicinoid microtubule inhibitors based on the styrylbenzothiazole (SBT) scaffold that are nonresponsive to typical fluorescent protein imaging wavelengths and so enable multichannel imaging studies. We applied these reagents both to 3D organoids and tissue explants and to classic model organisms (zebrafish, clawed frog) in one- and two-protein imaging experiments, in which spatiotemporally localized illuminations allowed them to photocontrol microtubule dynamics, network architecture, and microtubule-dependent processes in vivo with cellular precision and second-level resolution. These nanomolar, in vivo capable photoswitchable reagents should open up new dimensions for high-precision cytoskeleton research in cargo transport, cell motility, cell division, and development. More broadly, their design can also inspire similarly capable optical reagents for a range of cytosolic protein targets, thus bringing in vivo photopharmacology one step doser to general realization.American Chemical Society (ACS)2022info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/2445/186228Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésReproducció del document publicat a: https://doi.org/10.1021/jacs.2c01020Journal of the American Chemical Society, 2022, vol. 144, num. 12, p. 5614-5628https://doi.org/10.1021/jacs.2c01020cc by-nc-nd (c) Gao, Li et al, 2022http://creativecommons.org/licenses/by-nc-nd/3.0/es/info:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1862282026-05-27T06:46:51Z
dc.title.none.fl_str_mv In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M
title In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M
spellingShingle In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M
Gao, Li
Citosquelet
Mitosi
Cytoskeleton
Mitosis
title_short In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M
title_full In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M
title_fullStr In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M
title_full_unstemmed In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M
title_sort In Vivo Photocontrol of Microtubule Dynamics and Integrity, Migration and Mitosis, by the Potent GFP-Imaging-Compatible Photoswitchable Reagents SBTubA4P and SBTub2M
dc.creator.none.fl_str_mv Gao, Li
Meiring, Joyce C. M.
Varady, Adam
Ruider, Iris E.
Heise, Constanze
Wranik, Maximilian
Velasco, Cecilia D.
Taylor, Jennifer A.
Terni, Beatrice
Weinert, Tobias
Standfuss, Jörg
Cabernard, Clemens C.
Llobet Berenguer, Artur, 1972-
Steinmetz, Michel O.
Bausch, Andreas R.
Distel, Martin
Thorn-Seshold, Julia
Akhmanova, Anna
Thorn-Seshold, Oliver
author Gao, Li
author_facet Gao, Li
Meiring, Joyce C. M.
Varady, Adam
Ruider, Iris E.
Heise, Constanze
Wranik, Maximilian
Velasco, Cecilia D.
Taylor, Jennifer A.
Terni, Beatrice
Weinert, Tobias
Standfuss, Jörg
Cabernard, Clemens C.
Llobet Berenguer, Artur, 1972-
Steinmetz, Michel O.
Bausch, Andreas R.
Distel, Martin
Thorn-Seshold, Julia
Akhmanova, Anna
Thorn-Seshold, Oliver
author_role author
author2 Meiring, Joyce C. M.
Varady, Adam
Ruider, Iris E.
Heise, Constanze
Wranik, Maximilian
Velasco, Cecilia D.
Taylor, Jennifer A.
Terni, Beatrice
Weinert, Tobias
Standfuss, Jörg
Cabernard, Clemens C.
Llobet Berenguer, Artur, 1972-
Steinmetz, Michel O.
Bausch, Andreas R.
Distel, Martin
Thorn-Seshold, Julia
Akhmanova, Anna
Thorn-Seshold, Oliver
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Citosquelet
Mitosi
Cytoskeleton
Mitosis
topic Citosquelet
Mitosi
Cytoskeleton
Mitosis
description Photoswitchable reagents arc powerful tools for high-precision studies in cell biology. When these reagents are globally administered yet locally photoactivated in two-dimensional (2D) cell cultures, they can exert micron- and millisecond-scale biological control. This gives them great potential for use in biologically more relevant three-dimensional (3D) models and in vivo, particularly for studying systems with inherent spatiotemporal complexity, such as the cytoskeleton. However, due to a combination of photoswitch isomerization under typical imaging conditions, metabolic liabilities, and insufficient water solubility at effective concentrations, the in vivo potential of photoswitchable reagents addressing cytosolic protein targets remains largely unrealized. Here, we optimized the potency and solubility of metabolically stable, druglike colchicinoid microtubule inhibitors based on the styrylbenzothiazole (SBT) scaffold that are nonresponsive to typical fluorescent protein imaging wavelengths and so enable multichannel imaging studies. We applied these reagents both to 3D organoids and tissue explants and to classic model organisms (zebrafish, clawed frog) in one- and two-protein imaging experiments, in which spatiotemporally localized illuminations allowed them to photocontrol microtubule dynamics, network architecture, and microtubule-dependent processes in vivo with cellular precision and second-level resolution. These nanomolar, in vivo capable photoswitchable reagents should open up new dimensions for high-precision cytoskeleton research in cargo transport, cell motility, cell division, and development. More broadly, their design can also inspire similarly capable optical reagents for a range of cytosolic protein targets, thus bringing in vivo photopharmacology one step doser to general realization.
publishDate 2022
dc.date.none.fl_str_mv 2022
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/2445/186228
url https://hdl.handle.net/2445/186228
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Reproducció del document publicat a: https://doi.org/10.1021/jacs.2c01020
Journal of the American Chemical Society, 2022, vol. 144, num. 12, p. 5614-5628
https://doi.org/10.1021/jacs.2c01020
dc.rights.none.fl_str_mv cc by-nc-nd (c) Gao, Li et al, 2022
http://creativecommons.org/licenses/by-nc-nd/3.0/es/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv cc by-nc-nd (c) Gao, Li et al, 2022
http://creativecommons.org/licenses/by-nc-nd/3.0/es/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv American Chemical Society (ACS)
publisher.none.fl_str_mv American Chemical Society (ACS)
dc.source.none.fl_str_mv Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
reponame:Dipòsit Digital de la UB
instname:Universidad de Barcelona
instname_str Universidad de Barcelona
reponame_str Dipòsit Digital de la UB
collection Dipòsit Digital de la UB
repository.name.fl_str_mv
repository.mail.fl_str_mv
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