CRISPR

CRISPR Cas9 explained. CRISPR (clustered regularly interspaced short palindromic repeats) are segments of prokaryotic DNA containing short repetitions of base sequences. is an RNA-guided gene-editing platform that makes use of a bacterially derived protein (Cas9) and a synthetic guide RNA to introduce a double strand break at a specific location within the genome.

Cas9 is an enzyme that snips DNA, and CRISPR is a collection of DNA sequences that tells Cas9 exactly where to snip.

CRISPR pioneer Jennifer Doudna is co-founder of new biotech company

April 29, 2018

Mammoth Biosciences company announcedThe world is getting closer to using Crispr to detect a disease quickly, accurately, and cheaply thanks to a new company co-launched by Jennifer Doudna.

Brewing hoppy beer without the hops

March 20, 2018

CRISPR scissors, Cas12a, enables cutting-edge diagnostics

February 15, 2018

CRISPR-Cas12a TestingCRISPR-Cas12a, one of the DNA-cutting proteins revolutionizing biology today, has an unexpected side effect that makes it an ideal enzyme for simple, rapid and accurate disease diagnostics.  

National Academy of Sciences honors Raghavendra, Doudna

January 17, 2018

Jennifer DoudnaPrasad Raghavendra, an associate professor of electrical engineering and computer science, and Jennifer Doudna, a professor of molecular and cell biology and of chemistry, were honored this week by the National Academy of Sciences for their innovative body of research.

The future of biochemistry

January 12, 2018

ACS Biochemistry Issue CoverThe ACS January 2018 Special Biochemistry Issue has included College of Chemistry professors Ming Hammond, Evan Miller, and David Savage among the 44 early career scientists identified as representing the future of biochemistry. These scientists are noted by the publication for tackling problems of biological relevance.

Chocolate is on track to go extinct in 40 years

December 31, 2017

Student estimating amount of candy in beakerScientists at the University of California are teaming up with Mars company to try to save the crop before it's too late.

First step toward CRISPR cure of Lou Gehrig's disease

December 20, 2017

David SchafferDavid Schaffer and fellow UC Berkeley scientists have for the first time used CRISPR-Cas9 gene editing to disable a defective gene that causes amyotrophic lateral sclerosis, or Lou Gehrig's disease, in mice, extending their lifespan by 25 percent.

Watch Real Moving Images of CRISPR/Cas9 Cutting DNA

November 21, 2017

movie of DNA search and cleavage by CRISPR-Cas9 by Osamu NurekiResearcher Osamu Nureki used high‐speed atomic‐force microscopy to film a tiny needle move back and forth across Cas9.