| Literature DB >> 33542099 |
Hironori Takahashi1,2, Mako Kamiya1,3, Minoru Kawatani1, Keitaro Umezawa1, Yoshiaki Ukita4, Shinsuke Niwa5, Toshiyuki Oda6, Yasuteru Urano7,8,9.
Abstract
Caenorhabditis elegans is used as a model system to understand the neural basis of behavior, but application of caged compounds to manipulate and monitor the neural activity is hampered by the innate photophobic response of the nematode to short-wavelength light or by the low temporal resolution of photocontrol. Here, we develop boron dipyrromethene (BODIPY)-derived caged compounds that release bioactive phenol derivatives upon illumination in the yellow wavelength range. We show that activation of the transient receptor potential vanilloid 1 (TRPV1) cation channel by spatially targeted optical uncaging of the TRPV1 agonist N-vanillylnonanamide at 580 nm modulates neural activity. Further, neuronal activation by illumination-induced uncaging enables optical control of the behavior of freely moving C. elegans without inducing a photophobic response and without crosstalk between uncaging and simultaneous fluorescence monitoring of neural activity.Entities:
Keywords: C. elegans; caged compounds; fluorescence imaging; photocontrol; photolysis
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Year: 2021 PMID: 33542099 PMCID: PMC8017752 DOI: 10.1073/pnas.2009634118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205