Heavily and fully modified RNAs guide efficient SpyCas9-mediated genome editing
Resistance of gRNA to ubiquitous ribonucleases is required for CRISPR-Cas9-based therapeutics. Here, the authors explore chemical modifications at all positions of the crRNA guide and tracrRNA cofactor, and identify modified versions that are more potent and stable than their unmodified counterparts...
Enregistré dans:
Auteurs principaux: | Aamir Mir, Julia F. Alterman, Matthew R. Hassler, Alexandre J. Debacker, Edward Hudgens, Dimas Echeverria, Michael H. Brodsky, Anastasia Khvorova, Jonathan K. Watts, Erik J. Sontheimer |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2018
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/b945b146d35544ef9d5a4a30d633c3c0 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
The novel anti-CRISPR AcrIIA22 relieves DNA torsion in target plasmids and impairs SpyCas9 activity.
par: Kevin J Forsberg, et autres
Publié: (2021) -
Orthogonal Cas9–Cas9 chimeras provide a versatile platform for genome editing
par: Mehmet Fatih Bolukbasi, et autres
Publié: (2018) -
Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox
par: Irsyad N. A. Khairil Anuar, et autres
Publié: (2019) -
Publisher Correction: Orthogonal Cas9-Cas9 chimeras provide a versatile platform for genome editing
par: Mehmet Fatih Bolukbasi, et autres
Publié: (2018) -
Contemporary Approach to Heavily Calcified Coronary Lesions
par: Carlotta Sorini Dini, et autres
Publié: (2019)