This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility:

fact-checked

peer-reviewed publication

trusted source

proofread

New modified CRISPR protein can fit inside virus used for gene therapy

New, modified CRISPR protein can fit inside virus used for gene therapy
enEbCas12a enables all-in-one AAV delivery system. Credit: Chen Peng (CC-BY 4.0, creativecommons.org/licenses/by/4.0/)

Researchers have developed a novel version of a key CRISPR gene-editing protein that shows efficient editing activity and is small enough to be packaged within a non-pathogenic virus that can deliver it to target cells. Hongjian Wang and colleagues at Wuhan University, China, present these findings in the open-access journal PLOS Biology.

Recent years have seen an explosion of research attempting to harness CRISPR gene-editing systems—which are found naturally in many bacteria as a defense against viruses—so they can be used as potential treatments for human disease. These systems rely on so-called CRISPR-associated (Cas) proteins, with Cas9 and Cas12a being the two most widely used types, each with their own quirks and strengths.

One promising idea is to package CRISPR proteins within a non-pathogenic virus, which could then deliver the proteins to target cells; there, they would modify specifically targeted DNA sequences to treat disease. However, the commonly used adeno-associated virus is small, and while some Cas9 proteins can fit inside, Cas12a proteins are typically too large.

Now, Wang and colleagues have identified a relatively small version of Cas12a, termed EbCas12a, that occurs naturally in a species of the Erysipelotrichia class of bacteria. By deliberately switching out one of the amino acid building blocks of the protein for another, they boosted its gene-editing efficiency.

When applied to in a dish in the lab, this modified protein—dubbed enEbCas12a—shows gene-editing efficiency comparable to that of two other Cas12a proteins known for highly accurate gene editing.

The research team then demonstrated that enEbCas12a is small enough to be used for adeno-associated virus-based . They modified enEbCas12a to target a specific cholesterol-associated gene, packaged it within the virus, and administered the virus to mice with . One month later, they found a significant reduction of blood cholesterol levels in the treated mice, compared to mice that did not receive the virus.

More research will be needed to determine if enEbCas12a could one day be used to address . Nonetheless, these findings suggest it could be possible to use adeno-associated to deliver Cas12a proteins for gene therapy.

The authors add, "The novel compact enEbCas12a, along with its crRNA, can be packaged into an all-in-one AAV system for convenient gene editing in vitro and in vivo with high-fidelity, which can be very beneficial for future clinical applications and more tool developments including all-in-one AAV- based multi-gene editing, base editing, primer editing, etc."

More information: Wang H, Zhou J, Lei J, Mo G, Wu Y, Liu H, et al, Engineering of a compact, high-fidelity EbCas12a variant that can be packaged with its crRNA into an all-in-one AAV vector delivery system. PLoS Biology (2024). DOI: 10.1371/journal.pbio.3002619

Journal information: PLoS Biology

Citation: New modified CRISPR protein can fit inside virus used for gene therapy (2024, May 30) retrieved 25 June 2024 from https://phys.org/news/2024-05-crispr-protein-virus-gene-therapy.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Researchers develop prime editors using Cas12a and circular RNAs in human cells

213 shares

Feedback to editors