Newly engineered CRISPR enzyme for editing DNA is more compact yet just as efficient as current popular tool, and could improve patient treatment.
A new CRISPR-based gene-editing tool has been developed, which could lead to better treatments for patients with genetic disorders. The tool is an enzyme, AsCas12f, modified to offer the same effectiveness but at one-third the size of the Cas9 enzyme commonly used for gene editing.
The compact size means more of it can be packed into carrier viruses and delivered into living cells, making it more efficient. Researchers created a library of possible AsCas12f mutations and then combined selected ones to engineer an AsCas12f enzyme with 10 times more editing ability than the original unmutated type.
This engineered AsCas12f has already been successfully tested in mice and can potentially be used for new, more effective patient treatments.
Structural analysis and deep mutational scanning (DMS) of AsCas12f. The team used cryogenic electron microscopy to look at the structure of biological molecules in high-resolution, to analyze AsCas12f and engineer their new version. The DMS “heatmap” illustrates how all single mutations affected genome-editing activity. Blue squares indicate an undesirable mutation, while red ones represent desirable changes. The darker the color, the greater the effect. Image credit: Hino et al. 2023
By now you have probably heard of CRISPR, the gene-editing tool which enables researchers to replace and alter segments of DNA. Like genetic tailors, scientists have been experimenting with “snipping away” the genes that make mosquitoes malaria carriers, altering food crops to be more nutritious and delicious, and in recent years begun human trials to overcome some of the most challenging diseases and genetic disorders.
The potential of CRISPR to improve our lives is so phenomenal that in 2020, researchers Jennifer Doudna and Emmanuelle Charpentier, who developed the most precise version of the tool named CRISPR-Cas9, were awarded the Nobel Prize in chemistry.
But even Cas9 has limitations. The common way to deliver genetic material into a host cell is to use a modified virus as a carrier. Adeno-associated viruses (AAVs) are not harmful to patients, can enter many different types of cells to introduce CRISPR enzymes like Cas9, and are less likely to provoke an undesired immune response than other methods.
However, like any parcel delivery service, there is a size limit. “Cas9 is at the very limit of this size restriction, so there has been a demand for a smaller Cas protein that can be efficiently packaged into AAV and serve as a genome-editing tool,” explained Professor Osamu Nureki from the Department of Biological Sciences at the University of Tokyo.
Its large size means Cas9 can lack efficiency when used for gene therapy. So, a large multi-institutional team worked to develop a smaller Cas enzyme that is just as active, but more efficient. The researchers selected an enzyme called AsCas12f, from the bacteria Axidibacillus sulfuroxidans.
The advantage of this enzyme is that it is one of the most compact Cas enzymes found to date and less than one-third the size of Cas9. However, in previous tests it showed barely any genome activity in human cells.
Genome-editing ability of AsCas12f variants in three human cell lines. This graph shows how efficient two versions of the engineered AsCas12f enzyme are at gene editing (second and third columns in orange and yellow), compared to the original unengineered type (first column in gray), and the commonly used Cas9 type (fourth column in blue). The higher the bar, the more efficient the tool. Image credit: Hino et al. 2023
“Using a screening method called deep mutational scanning, we assembled a library of potential new candidates by substituting each amino acid residue of AsCas12f with all 20 types of amino acids on which all life is based. We identified over 200 mutations that enhanced genome-editing activity from this,” explained Nureki.
“Based on insights gained from the structural analysis of AsCas12f, we selected and combined these enhanced-activity amino acid mutations to create a modified AsCas12f. This engineered AsCas12f has more than 10 times the genome-editing activity compared to the usual AsCas12f type and is comparable to Cas9, while maintaining a much smaller size.”
The team has already carried out animal trials with the engineered AsCas12f system, partnering it with other genes and administering it to live mice. Administering treatments directly into the body is preferable to extracting cells, editing them in a lab and reinserting them into patients, which is more time-intensive and costly.
The success of the tests showed that engineered AsCas12f has the potential to be used for human gene therapies, such as treating hemophilia, a disease in which the blood does not clot normally.
The team discovered numerous potentially effective combinations for engineering an improved AsCas12f gene-editing system, so the researchers acknowledge the possibility that the selected mutations may not have been the most optimal of all the available mixes.
As a next step, computational modeling or machine learning could be used to sift through the combinations and predict which might offer even better improvements.
“Elevating AsCas12f to exhibit genome-editing activity comparable to that of Cas9 is a significant achievement and a substantial step in developing new, more compact genome-editing tools,” said Nureki.
“For us the crucial aspect of gene therapy is its potential to help patients genuinely. Using the engineered AsCas12f we developed, our next challenge is administering gene therapy to aid people suffering from genetic disorders.”
Source: University of Tokyo