The clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 system is a powerful and widely used tool for genome editing. Recently, it was reported that direct delivery of Cas9-sgRNA ribonucleoproteins (RNPs) reduced off-target effects. Therefore, non-invasive, high-throughput methods are needed for direct delivery of RNPs into cells. Here, we report a novel method for direct delivery of RNPs into cells using a nanostructure with a high-aspect-ratio and uniform nanoneedles. This nanostructure is composed of tens of thousands of nanoneedles laid across a 2D array. Through insertion of the nanoneedle array previously adsorbed with Cas9-sgRNA, it was possible to deliver RNPs directly into mammalian cells for genome editing
The clustered regularly interspaced short palindromic repeats (CRISPR)/associated protein (CRISPR/Ca...
Delivery is a key challenge in novel protein therapeutic development. Even though numerous proteins ...
International audienceProgrammable nucleases have enabled rapid and accessible genome engineering in...
The clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (CRISPR/...
© 2022 Elsevier B.V.Programmable endonucleases such as CRISPR/Cas9 system emerge as a promising tool...
Genome editing through the delivery of CRISPR/Cas9-ribonucleoprotein (Cas9-RNP) reduces unwanted gen...
CRISPR-Cas9 represents a promising technology for genome editing, yet means of safe and efficient de...
Therapeutic targets of CRISPR-Cas can often not be accessed due to lack of carriers to deliver RNPs ...
In recent years, CRISPR-Cas9 technology has shown promise as a versatile gene editing tool that ena...
There is a critical need for the development of safe and efficient delivery technologies for CRISPR/...
A transient cytosolic delivery system for accurate Cas9 ribonucleoprotein is a key factor for target...
DNA nanostructures are a promising tool to deliver molecular payloads to cells. DNA origami structur...
Abstract The programmable endonuclease activity and simple usage of CRISPR/Cas9 have revolutionized...
Key to the widespread and secure application of genome editing tools is the safe and effective deliv...
RNA-guided engineered nucleases (RGENs) derived from the prokaryotic adaptive immune system known as...
The clustered regularly interspaced short palindromic repeats (CRISPR)/associated protein (CRISPR/Ca...
Delivery is a key challenge in novel protein therapeutic development. Even though numerous proteins ...
International audienceProgrammable nucleases have enabled rapid and accessible genome engineering in...
The clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (CRISPR/...
© 2022 Elsevier B.V.Programmable endonucleases such as CRISPR/Cas9 system emerge as a promising tool...
Genome editing through the delivery of CRISPR/Cas9-ribonucleoprotein (Cas9-RNP) reduces unwanted gen...
CRISPR-Cas9 represents a promising technology for genome editing, yet means of safe and efficient de...
Therapeutic targets of CRISPR-Cas can often not be accessed due to lack of carriers to deliver RNPs ...
In recent years, CRISPR-Cas9 technology has shown promise as a versatile gene editing tool that ena...
There is a critical need for the development of safe and efficient delivery technologies for CRISPR/...
A transient cytosolic delivery system for accurate Cas9 ribonucleoprotein is a key factor for target...
DNA nanostructures are a promising tool to deliver molecular payloads to cells. DNA origami structur...
Abstract The programmable endonuclease activity and simple usage of CRISPR/Cas9 have revolutionized...
Key to the widespread and secure application of genome editing tools is the safe and effective deliv...
RNA-guided engineered nucleases (RGENs) derived from the prokaryotic adaptive immune system known as...
The clustered regularly interspaced short palindromic repeats (CRISPR)/associated protein (CRISPR/Ca...
Delivery is a key challenge in novel protein therapeutic development. Even though numerous proteins ...
International audienceProgrammable nucleases have enabled rapid and accessible genome engineering in...