'Caged' peptide nucleic acids activated by red light in a singlet oxygen mediated process
Koenig SG, Mokhir A (2013)
Publication Type: Journal article, Original article
Publication year: 2013
Journal
Original Authors: König S.G., Mokhir A.
Publisher: Elsevier
Book Volume: 23
Pages Range: 6544-6548
Journal Issue: 24
DOI: 10.1016/j.bmcl.2013.11.003
Abstract
Common 'caged' nucleic acid binders, which can be applied for temporal and spatial control of gene expression, are activated by high energy light (<450 nm). The light of this type is damaging to cells and is strongly absorbed by cellular components. Therefore, shifting the triggering light to the visible region (>550 nm) is highly desirable. Herein we report on a cyclic peptide nucleic acid (PNA), whose backbone contains a 9,10-dialkoxy-substituted anthracene linker. The sequence of this compound was selected to be complementary to a representative microRNA (miR-92). We demonstrated that the cyclic PNA does not bind complementary nucleic acids and is, correspondingly, 'caged'. Its uncaging can be conducted by its exposure to red light (635 nm) in the presence of pyropheophorbide-a. The latter process is mediated by singlet oxygen (O), which cleaves the 9,10-dialcoxyanthracene linker within the PNA with formation of a linear PNA, an efficient binder of the complementary ribonucleic acid. This is the first example of a red light-activated, 'caged' peptide nucleic acid. © 2013 Elsevier Ltd. All rights reserved.
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APA:
Koenig, S.G., & Mokhir, A. (2013). 'Caged' peptide nucleic acids activated by red light in a singlet oxygen mediated process. Bioorganic & Medicinal Chemistry Letters, 23(24), 6544-6548. https://doi.org/10.1016/j.bmcl.2013.11.003
MLA:
Koenig, Sandra G., and Andriy Mokhir. "'Caged' peptide nucleic acids activated by red light in a singlet oxygen mediated process." Bioorganic & Medicinal Chemistry Letters 23.24 (2013): 6544-6548.
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