TY - JOUR
T1 - Photochemical Barcodes
AU - Tang, Sicheng
AU - Zhang, Yang
AU - Dhakal, Pravat
AU - Ravelo, Laura
AU - Anderson, Cheyenne L.
AU - Collins, Kevin M.
AU - Raymo, Françisco M.
N1 - Funding Information:
The National Institutes of Health (NS086932) and National Science Foundation (CHE-1505885) are acknowledged for financial support.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/4/4
Y1 - 2018/4/4
N2 - A photochemical strategy to encode fluorescence signals in vivo with spatial control was designed around the unique properties of a photoactivatable borondipyrromethene (BODIPY). The photoinduced disconnection of two oxazines, flanking a single BODIPY, in two consecutive steps produces a mixture of three emissive molecules with resolved fluorescence inside polymer beads. The relative amounts and emission intensities of the three fluorophores can be regulated precisely in each bead by adjusting the dose of activating photons to mark individual particles with distinct codes of fluorescence signals. The visible wavelengths and mild illumination sufficient to induce these transformations permit the photochemical barcoding of beads also in living nematodes. Different regions of the same animal can be labeled with distinct barcodes to allow the monitoring of their dynamics for long times with no toxic effects. Thus, our photochemical strategy for the generation of fluorescence barcodes can produce multiple and distinguishable labels in the same biological sample to enable the spatiotemporal tracking of, otherwise indistinguishable, targets.
AB - A photochemical strategy to encode fluorescence signals in vivo with spatial control was designed around the unique properties of a photoactivatable borondipyrromethene (BODIPY). The photoinduced disconnection of two oxazines, flanking a single BODIPY, in two consecutive steps produces a mixture of three emissive molecules with resolved fluorescence inside polymer beads. The relative amounts and emission intensities of the three fluorophores can be regulated precisely in each bead by adjusting the dose of activating photons to mark individual particles with distinct codes of fluorescence signals. The visible wavelengths and mild illumination sufficient to induce these transformations permit the photochemical barcoding of beads also in living nematodes. Different regions of the same animal can be labeled with distinct barcodes to allow the monitoring of their dynamics for long times with no toxic effects. Thus, our photochemical strategy for the generation of fluorescence barcodes can produce multiple and distinguishable labels in the same biological sample to enable the spatiotemporal tracking of, otherwise indistinguishable, targets.
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U2 - 10.1021/jacs.8b00887
DO - 10.1021/jacs.8b00887
M3 - Article
C2 - 29561604
AN - SCOPUS:85044919203
SN - 0002-7863
VL - 140
SP - 4485
EP - 4488
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 13
ER -