Other CRISPR Tools

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A partial CRISPR prime editing schematic cartoon. The parts of the prime editor and pegRNA are indicated. The prime editor consists of a Cas9n H840A nickase fused to a reverse transcriptase (RT), while the pegRNA includes spacer, scaffold, RT template, and primer binding site (PBS) sequences. The desired edit is part of the RT template. In the first step, these components form a complex, bind target DNA, and nick the Cas9 non-target strand. An arrow leads to additional steps not shown in this preview.
A protein structure of ABE8e is shown, superimposed with cartoon representations of sgRNA and target DNA. Two TadA domains are highlighted. The catalytic domain contacts multiple bases of the non-target DNA strand, while the docking domain primarily contacts the other protein domains.
Cartoon of CRISPR-associated transposase (CAST) integrating donor DNA into a genomic target site.
Diagram of the Cascade complex with gRNA bound to target DNA, after recruitment of Cas3. Cas3 is about to nick the non-target strand.
A cartoon of a prime editor with two different edit sequences. The DNA sequences are shown with one strand edited and a 5′ DNA flap, before heteroduplex resolution and DNA repair.  The first edit has an unchanged PAM. This DNA is shown connected to the prime editor by a two-way arrow, indicating that the editor can re-bind. Re-nicking is represented by scissors and would remove the newly edited DNA.  The second edit has an altered PAM. A one-way arrow leads from the prime editor to this edit, indicating that the changed PAM prevents the editor from re-binding.
screenshot of various PRIDICT webpages
schematic representation of the PASTE system
Using CRISPR in C. elegans to knock-in FLAG tag.

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