Research published today in Nature Chemical Biology reveals new opportunities for using small molecule drugs to target KRAS, the most commonly mutated protein in cancer. Promega research scientists collaborated with the University of California – San Francisco research group led by Dr. Kevan M. Shokat, a global leader in KRAS biology, to study the binding of potentially therapeutic molecules to common mutants of the KRAS protein. This study represents the first observation and quantification of direct target engagement of KRAS(G12D) and other hotspot oncogenic mutants of KRAS in cells using reversible binders.
KRAS and cancer
KRAS is a protein that serves as a “master switch” for regulating cell proliferation. It is the most commonly mutated protein in cancer. KRAS was long considered to be “undruggable” until 2013 when the Shokat lab identified covalent drugs targeting KRAS(G12C), a common mutant in which a glycine amino acid is changed to a cysteine. That discovery led to increased drug discovery research, and eventually the first inhibitors targeting KRAS(G12C).
Unfortunately, other mutants of KRAS presented different challenges. All of the known inhibitors of KRAS(G12C) relied on an inactive state of the protein that other mutants do not frequently exhibit. The G12C mutation also provided the opportunity to employ covalent drug discovery methods that would not apply to other hotspot mutants. For those reasons, alleles such as KRAS(G12D) and KRAS(G12V) continued to be considered undruggable.
Targeting hotspot mutants for drug discovery
The research published today in Nature Chemical Biology utilized a Bioluminescence Resonance Energy Transfer (BRET) assay to quantify target engagement of RAS complexes in live cells. They found that the switch-II pocket of KRAS was a privileged drug binding site for non-covalent ligands, and that this was not dependent on the activation state of KRAS. These results open new opportunities for targeting non-G12C mutants of KRAS in drug discovery.
“We’ve shown that some of these highly aggressive mutants are indeed vulnerable to small molecule inhibitors,” says Matt Robers, Senior Research Scientist at Promega.
With our new target engagement method, we can measure binding within living cells and show that the binding we see at these hotspot mutants actually translates into anti-proliferative effects in the pancreatic cancer lineages.”
Matt Robers, Senior Research Scientist, Promega
In addition to the BRET methods for measuring target engagement, the paper also describes nuclear magnetic resonance (NMR) spectroscopy methods for observing reversible ligand binding in vitro and determining the state of the KRAS protein. The authors hope that the methods they describe will be a valuable tool for researchers to develop treatments for some of the most aggressive KRAS mutants previously thought to be “undruggable.”
Promega offers a comprehensive selection of tools to accelerate RAS pathway drug discovery based on a sensitive bioluminescence platform.
