CRISPR CAS 9 Clustered regularly inter spaced short palindromic repeats
CRISPR CAS 9 Clustered regularly inter spaced short palindromic repeats. segments of prokaryotic DNA containing short repetitions of base sequences. gene editing, genome editing 3d render

An adapted CRISPR protein that targets RNA can serve as a rapid, inexpensive, and sensitive diagnostic tool say researchers from the Broad Institute of MIT and Harvard, the McGovern Institute for Brain Research at MIT, the Institute for Medical Engineering & Science at MIT, and the Wyss Institute for Biologically Inspired Engineering at Harvard University. The new tool, dubbed SHERLOCK (Specific High-sensitivity Enzymatic Reporter unLOCKing), could one day be used to respond to viral and bacterial outbreaks, monitor antibiotic resistance, and detect cancer, according to the researchers.

Details of this tool were recently published in Science (“Nucleic Acid Detection with CRISPR-Cas13a/C2c2”), wherein Broad institute investigators describe how this RNA-targeting CRISPR enzyme was harnessed as a sensitive detector that was able to indicate the presence of as little as a single molecule of a target RNA or DNA molecule.

Specifically, the scientists say they demonstrated the method's versatility on a range of applications, including detecting the presence of Zika virus in patient blood or urine samples within hours, distinguishing between the genetic sequences of African and American strains of Zika virus, discriminating specific types of bacteria, such as Escherichia coli, detecting antibiotic resistance genes, identifying  cancerous mutations in simulated cell-free DNA fragments, and reading human genetic information, such as risk of heart disease, from a saliva sample.

Because the tool can be designed for use as a paper-based test that does not require refrigeration, the researchers say it is well suited for fast deployment and widespread use inside and outside of traditional settings, such as at a field hospital during an outbreak or a rural clinic with limited access to advanced equipment.

“It's exciting that the Cas13a enzyme, which was originally identified in our collaboration with Eugene Koonin, Ph.D. (National Center for Biotechnology Information) to study the basic biology of bacterial immunity, can be harnessed to achieve such extraordinary sensitivity, which will be powerful for both science and clinical medicine,” said Feng Zhang, Ph.D., core institute member of the Broad Institute, an investigator at the McGovern Institute for Brain Research at MIT, and the James and Patricia Poitras '63 Professor in Neuroscience and associate professor in Brain and Cognitive Sciences and Biological Engineering at MIT.

In June 2016, Zhang and his colleagues characterized the RNA-targeting CRISPR enzyme, which is now called Cas13a (previously known as C2c2) and can be programmed to cleave particular RNA sequences in bacterial cells. Unlike DNA-targeting CRISPR enzymes (such as Cas9 and Cpf1), Cas13a reportedly can remain active after cutting its intended RNA target and may exhibit promiscuous behavior, continuing to cut other nontargeted RNAs in a burst of activity that Zhang lab scientists referred to as “collateral cleavage.” In their paper and patent filing, the team described a wide range of biotechnological applications for the system, including harnessing RNA cleavage and collateral activity for basic research, diagnostics, and therapeutics. 

The highly sensitive test was cited as the result of a collaboration between Zhang and his team and Broad institute member Jim Collins, Ph.D., who had been working on diagnostics for Zika virus. In 2014, Collins and his team at the Wyss Institute created a rapid, synthetic paper-based test for the Ebola virus that can be shipped and stored at room temperature. They later modified the system to detect Zika virus and demonstrated they were able to increase the sensitivity of the sensor by boosting the amount of RNA in the sample using low-levels of applied heat.

Working together, the Zhang and Collins teams were able to use a different amplification process, relying on body heat, to boost the levels of DNA or RNA in their test samples. Once the level was increased, the team applied a second amplification step to convert the DNA to RNA, which enabled them to increase the sensitivity of the RNA-targeting CRISPR by a millionfold.

“We can now effectively and readily make sensors for any nucleic acid, which is incredibly powerful when you think of diagnostics and research applications,” said Dr. Collins, Termeer Professor of Bioengineering at MIT and core faculty member at the Wyss Institute for Biologically Inspired Engineering at Harvard. “This tool offers the sensitivity that could detect an extremely small amount of cancer DNA in a patient's blood sample, for example, which would help researchers understand how cancer mutates over time. For public health, it could help researchers monitor the frequency of antibiotic-resistant bacteria in a population. The scientific possibilities get very exciting very quickly.”

Also of Interest