We've updated our Privacy Policy to make it clearer how we use your personal data.

We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Controlling CRISPR/Cas9 Gene Editing with Light
Industry Insight

Controlling CRISPR/Cas9 Gene Editing with Light

Controlling CRISPR/Cas9 Gene Editing with Light
Industry Insight

Controlling CRISPR/Cas9 Gene Editing with Light

Want a FREE PDF version of This Industry Insight?

Complete the form below and we will email you a PDF version of "Controlling CRISPR/Cas9 Gene Editing with Light"

First Name*
Last Name*
Email Address*
Company Type*
Job Function*
Would you like to receive further email communication from Technology Networks?

Technology Networks Ltd. needs the contact information you provide to us to contact you about our products and services. You may unsubscribe from these communications at any time. For information on how to unsubscribe, as well as our privacy practices and commitment to protecting your privacy, check out our Privacy Policy

For a long time, scientists have been trying to manipulate genes. Recently, at the University of Pittsburgh Alexander Deiters found a way to control this process with higher accuracy using light. This breakthrough by Deiters and his team was recently published the Journal of the American Chemical Society.

In 2013, scientists began using a gene editing tool called CRISPR/Cas9. This method uses a bacterial derived protein (Cas9) and a synthetic guide RNA, causing double strand breaks at specific locations of the genome. Allowing researchers to remove a gene, change its function, or introduce a desired mutation.

In fact, CRISPR has shown great promise, which enables researchers to treat cystic fibrosis and sickle cell anemia, establish experimental animal models simulating human disease and cultivate wheat lines resistant to powdery mildew disease. More details can be found here 

Through a series of experiments, Alexander Deiters, Professor of Chemistry  at the University of Pittsburgh School and Kenneth P. Dietrich and colleagues at the University of North Carolina at Chapel Hill, have found a lysine residue (lysine is an amino acid) in Cas9 which can be replaced by analogues activated by light. This method, developed by Deiters, generates a non-functional Cas9 protein called "caged". The "cage" will be removed only by exposure to activate enzyme and thereby activate gene editing.

Deiters said: "This method can aid in the better design of cells or animal genes with both space and time control. Previously, if you want to knock out a gene, control is limited to the time and place genes appear. The design of a light switch in Cas, provides a more accurate editing tool. You can say, 'in this cell, at this point, at this time I want to modify the genome regions'."
Deiters points out that, after the improvement and with the passage of time, controlling the place in which a gene will be manipulated may contribute to the elimination of "distance effect".

About the author
Creative Animodel is serving CRISPR/Cas9 service for a long time. It also provides animal model of diseases, knock out or knock in service. If you want to know more about animal model of diseases, visit Animal Model Development