2019
DOI: 10.1002/ange.201908105
|View full text |Cite
|
Sign up to set email alerts
|

Orthogonal Activation of RNA‐Cleaving DNAzymes in Live Cells by Reactive Oxygen Species

Abstract: RNA‐cleaving DNAzymes are useful tools for intracellular metal‐ion sensing and gene regulation. Incorporating stimuli‐responsive modifications into these DNAzymes enables their activities to be spatiotemporally and chemically controlled for more precise applications. Despite the successful development of many caged DNAzymes for light‐induced activation, DNAzymes that can be intracellularly activated by chemical inputs of biological importance, such as reactive oxygen species (ROS), are still scarce. ROS like h… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2019
2019
2022
2022

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 17 publications
(1 citation statement)
references
References 66 publications
0
1
0
Order By: Relevance
“…Further by combination of the caged DNAzymes with upconversion nanoparticles (UCNPs), they realized the activation of DNAzyme activity in an NIR region [44] . In 2019, the Xiang Lab constructed an reactive oxygen species (ROS) activated DNAzyme by incorporation PS or phenylboronate groups at specific backbone positions in 8–17 DNAzyme by the efficient chemical conjugation reaction [45] . The Shionoya group demonstrated the concept of sharp switching of DNAzyme activity by introducing a Cu II ‐mediated carboxyimidazole base pair (ImC−Cu II −ImC) in the splitted catalytic core of E5 DNAzyme [46] .…”
Section: Expanding Of Dnazyme Librarymentioning
confidence: 99%
“…Further by combination of the caged DNAzymes with upconversion nanoparticles (UCNPs), they realized the activation of DNAzyme activity in an NIR region [44] . In 2019, the Xiang Lab constructed an reactive oxygen species (ROS) activated DNAzyme by incorporation PS or phenylboronate groups at specific backbone positions in 8–17 DNAzyme by the efficient chemical conjugation reaction [45] . The Shionoya group demonstrated the concept of sharp switching of DNAzyme activity by introducing a Cu II ‐mediated carboxyimidazole base pair (ImC−Cu II −ImC) in the splitted catalytic core of E5 DNAzyme [46] .…”
Section: Expanding Of Dnazyme Librarymentioning
confidence: 99%