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Dual Near Infrared Two-Photon Microscopy for Deep-Tissue Dopamine Nanosensor Imaging

Jackson T. Del Bonis-O’Donnell, Ralph H. Page, Abraham G. Beyene, Eric G. Tindall, Ian McFarlane, Markita P. Landry
doi: https://doi.org/10.1101/145912
Jackson T. Del Bonis-O’Donnell
1Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720
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Ralph H. Page
1Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720
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Abraham G. Beyene
1Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720
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Eric G. Tindall
1Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720
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Ian McFarlane
1Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720
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Markita P. Landry
1Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720
2California Institute for Quantitative Biosciences, QB3, University of California, Berkeley, CA 94720
3Chan-Zuckerberg Biohub, San Francisco, CA 94158
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Abstract

A key limitation for achieving deep imaging in biological structures lies in photon absorption and scattering leading to attenuation of fluorescence. In particular, neurotransmitter imaging is challenging in the biologically-relevant context of the intact brain, for which photons must traverse the cranium, skin and bone. Thus, fluorescence imaging is limited to the surface cortical layers of the brain, only achievable with craniotomy. Herein, we describe optimal excitation and emission wavelengths for through-cranium imaging, and demonstrate that near-infrared emissive nanosensors can be photoexcited using a two-photon 1560 nm excitation source. Dopamine-sensitive nanosensors can undergo two-photon excitation, and provide chirality-dependent responses selective for dopamine with fluorescent turn-on responses varying between 20% and 350%. We further calculate the two-photon absorption cross-section and quantum yield of dopamine nanosensors, and confirm a two-photon power law relationship for the nanosensor excitation process. Finally, we show improved image quality of the nanosensors embedded 2 mm deep into a brain-mimetic tissue phantom, whereby one-photon excitation yields 42% scattering, in contrast to 4% scattering when the same object is imaged under two-photon excitation. Our approach overcomes traditional limitations in deep-tissue fluorescence microscopy, and can enable neurotransmitter imaging in the biologically-relevant milieu of the intact and living brain.

Footnotes

  • ↵* E-mail: landry{at}berkeley.edu

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Posted July 19, 2017.
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Dual Near Infrared Two-Photon Microscopy for Deep-Tissue Dopamine Nanosensor Imaging
Jackson T. Del Bonis-O’Donnell, Ralph H. Page, Abraham G. Beyene, Eric G. Tindall, Ian McFarlane, Markita P. Landry
bioRxiv 145912; doi: https://doi.org/10.1101/145912
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Dual Near Infrared Two-Photon Microscopy for Deep-Tissue Dopamine Nanosensor Imaging
Jackson T. Del Bonis-O’Donnell, Ralph H. Page, Abraham G. Beyene, Eric G. Tindall, Ian McFarlane, Markita P. Landry
bioRxiv 145912; doi: https://doi.org/10.1101/145912

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