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CRISPR Gene-Editing Used to Block Cobra Venom

Researchers Identify New Ways to Neutralize Venom

Scientists at the University of Sydney and Liverpool School of Tropical Medicine have made significant progress in developing ways to block cobra venom using CRISPR gene-editing technology.

In a recent study, the team used CRISPR to identify and inactivate genes in venom that are responsible for its toxic effects. This breakthrough opens up new avenues for the development of antivenom therapies, which are currently limited and often ineffective against certain types of snake venom.

The researchers focused on cobra venom, which contains a variety of toxins that can cause severe symptoms, including pain, swelling, and tissue damage. They used CRISPR to target specific genes in the venom that are responsible for these effects, and found that they could successfully neutralize them.

The study highlights the potential of CRISPR gene-editing technology to revolutionize the field of venom research and antivenom development. By precisely targeting and inactivating specific genes, researchers can develop more effective and targeted treatments for snakebite victims.

The team's findings were published in the journal Nature Biotechnology, and their work is expected to contribute to the development of novel and more effective antivenom therapies in the future.