TY - JOUR
T1 - Organelle-Targeted BODIPY Photocages
T2 - Visible-Light-Mediated Subcellular Photorelease
AU - Kand, Dnyaneshwar
AU - Pizarro, Lorena
AU - Angel, Inbar
AU - Avni, Adi
AU - Friedmann-Morvinski, Dinorah
AU - Weinstain, Roy
N1 - Publisher Copyright: © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/3/26
Y1 - 2019/3/26
N2 - Photocaging facilitates non-invasive and precise spatio-temporal control over the release of biologically relevant small- and macro-molecules using light. However, sub-cellular organelles are dispersed in cells in a manner that renders selective light-irradiation of a complete organelle impractical. Organelle-specific photocages could provide a powerful method for releasing bioactive molecules in sub-cellular locations. Herein, we report a general post-synthetic method for the chemical functionalization and further conjugation of meso-methyl BODIPY photocages and the synthesis of endoplasmic reticulum (ER)-, lysosome-, and mitochondria-targeted derivatives. We also demonstrate that 2,4-dinitrophenol, a mitochondrial uncoupler, and puromycin, a protein biosynthesis inhibitor, can be selectively photoreleased in mitochondria and ER, respectively, in live cells by using visible light. Additionally, photocaging is shown to lead to higher efficacy of the released molecules, probably owing to a localized and abrupt release.
AB - Photocaging facilitates non-invasive and precise spatio-temporal control over the release of biologically relevant small- and macro-molecules using light. However, sub-cellular organelles are dispersed in cells in a manner that renders selective light-irradiation of a complete organelle impractical. Organelle-specific photocages could provide a powerful method for releasing bioactive molecules in sub-cellular locations. Herein, we report a general post-synthetic method for the chemical functionalization and further conjugation of meso-methyl BODIPY photocages and the synthesis of endoplasmic reticulum (ER)-, lysosome-, and mitochondria-targeted derivatives. We also demonstrate that 2,4-dinitrophenol, a mitochondrial uncoupler, and puromycin, a protein biosynthesis inhibitor, can be selectively photoreleased in mitochondria and ER, respectively, in live cells by using visible light. Additionally, photocaging is shown to lead to higher efficacy of the released molecules, probably owing to a localized and abrupt release.
KW - BODIPY
KW - mitochondria
KW - organelles
KW - photo-release
KW - photocages
UR - http://www.scopus.com/inward/record.url?scp=85062351043&partnerID=8YFLogxK
U2 - https://doi.org/10.1002/anie.201900850
DO - https://doi.org/10.1002/anie.201900850
M3 - مقالة
C2 - 30731033
SN - 1433-7851
VL - 58
SP - 4659
EP - 4663
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 14
ER -