Location:
dPspCas13b-ADAT2 nuclease

dPspCas13b-ADAT2 RNA Editing Nuclease


Product Introduction

dPspCas13b-ADAT2 is an RNA editing tool based on CRISPR technology, serving as a core component of the REPAIR (RNA Editing for Programmable A to I Replacement) system. This fusion protein consists of a catalytically inactive Prevotella sp. P5-125 Cas13b (dPspCas13b) fused with the ADAT2 adenosine deaminase domain, enabling precise base editing at the RNA level and providing a novel strategy for correcting pathogenic RNA mutations.

Cas13b is a type VI-B CRISPR effector protein whose natural function is to target and bind RNA molecules. By introducing key mutations to inactivate its HPN nuclease domains, dPspCas13b completely loses its RNA cleavage activity while fully retaining the ability to specifically bind target RNA sequences guided by CRISPR RNA (crRNA), establishing it as a precise RNA targeting platform. ADAT2 is an adenosine deaminase naturally involved in tRNA modification that catalyzes the hydrolytic deamination of adenosine (A) to inosine (I). Since inosine is recognized as guanosine (G) by the ribosome during translation, A-to-I editing effectively achieves an A-to-G functional alteration.

When the crRNA guides dPspCas13b-ADAT2 to bind to a target transcript, ADAT2 locally deaminates specific adenosine positions, enabling precise RNA sequence recoding.

Product Specifications

Parameter

Specification

Source

Recombinant expression in E. coli

Molecular Weight

~150 kDa

Concentration

20 µM

Target Type

RNA

Editing Type

A-to-I (functionally equivalent to A-to-G)

PFS Requirement

No strict restriction

Purity

≥95% (SDS-PAGE)

Endotoxin

<1 EU/μg

Storage Buffer

50 mM Tris-HCl, 300 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 50% Glycerol

10× Reaction Buffer

50 mM Tris-HCl, 100 mM NaCl, 10 mM MgCl₂, 100 μg/ml BSA, pH 7.9

Storage Conditions

Long-term storage at -80°C; short-term storage at -20°C

Product Specifications

Specifications

Catalog Number

Concentration

Volume

100 pmol

GR101301

20 μM

5 μL

500 pmol

GR101302

20 μM

25 μL

2500 pmol

GR101303

20 μM

125 μL

Application Scenarios

RNA-level Mutation Correction: Repairing pathogenic RNA mutations without affecting the genome.

Reversible Gene Regulation: Temporarily modifying RNA information.

Protein Function Regulation: Altering protein sequences through RNA editing.

Disease Mechanism Studies: Investigating the role of RNA editing in diseases.

Editing in Non-dividing Cells: RNA editing independent of cell division.

References

Cox DBT, et al. (2017). RNA editing with CRISPR-Cas13. Science. 358(6366):1019-1027.

Abudayyeh OO, et al. (2019). A cytosine deaminase for programmable single-base RNA editing. Science. 365(6451):382-386.