Scripps Florida Scientists Uncover Most Detailed Picture Yet of Muscular Dystrophy Defect en Design Targeted New Drug Candidates

Scripps Florida Scientists Uncover Most Detailed Picture Yet of Muscular Dystrophy Defect then Design Targeted New Drug Candidates JUPITER, FL, January 2, 2014 Scientists from the Florida campus of The Scripps Research Institute have revealed an atomic-level view of a genetic defect that causes a form of muscular dystrophy, myotonic dystrophy type 2, and have used this information to design drug candidates with potential to counter those defects and reverse the disease.

This the first time the structure of the RNA defect that causes this disease has been determined, said TSRI Associate Professor Matthew Disney, who led the study. Based on these results, we designed compounds that, even in small amounts, significantly improve disease-associated defects in treated cells.

Myotonic dystrophy type 2 is a relatively rare form of muscular dystrophy that is somewhat milder than myotonic dystrophy type 1, the most common adult-onset form of the disease.

Both types of myotonic dystrophy are inherited disorders that involve progressive muscle wasting and weakness, and both are caused by a type of genetic defect known as a RNA repeat expansion, a series of nucleotides repeated more times than normal in an individual's genetic code. The repeat binds to the protein MBNL1, rendering it inactive and resulting in RNA splicing abnormalities which lead to the disease.

Many other researchers had tried to find the atomic-level structure of the myotonic dystrophy 2 repeat, but had run into technical difficulties. In a technique called X-ray crystallography, which is used to find detailed structural information, scientists manipulate a molecule so that a crystal forms. This crystal is then placed in a beam of X-rays, which diffract when they strike the atoms in the crystal. Based on the pattern of diffraction, scientists can then reconstruct the shape of the original molecule.

Prior to the new research, which was published in an advance, online issue of the journal ACS Chemical Biology, scientists had not been able to crystallize the problematic RNA. The Scripps Florida team spent several years on the problem and succeeded in engineering the RNA to have crystal contacts in different positions. This allowed the RNA to be crystallized and its structure to be revealed.

Using information about the RNA's structure and movement, the scientists were able to design molecules to improve RNA function.

The new findings were confirmed using sophisticated computational models that show precisely how the small molecules interact with and alter the RNA structure over time. Those predictive models matched what the scientists found in the study that these new compounds bind to the repeat structure in a predictable and easily reproducible way, attacking the cause of the disease.

We used a bottom-up approach, by first understanding how the small components of the RNA structure interact with small molecules, said Jessica Childs-Disney of TSRI, who was first author of the paper with Ilyas Yildirim of Northwestern University. The fact that our compounds improve the defects shows that our unconventional approach works.

In addition to Disney, Childs-Disney and Yildirim authors of the study, Myotonic Dystrophy Type 2 RNA: Structural Studies and Designed Small Molecules that Modulate RNA Function, include Jeremy Lohman, Lirui Guan, Tuan Tran, and HaJeung Park of TSRI; Partha Sarkar of the University of Texas Medical Branch and George C. Schatz of Northwestern University. For more information on the study, see http://pubs.acs.org/doi/abs/10.1021/cb4007387

The study was supported by the National Institutes of Health (grant R01 GM079235), the Muscular Dystrophy Association (grant 254929), TSRI and the PS-OC Center of the NIH (grant 1U54CA143869-01).

About The Scripps Research Institute

The Scripps Research Institute (TSRI) is one of the worlds largest independent, not-for-profit organizations focusing on research in the biomedical sciences. TSRI is internationally recognized for its contributions to science and health, including its role in laying the foundation for new treatments for cancer, rheumatoid arthritis, hemophilia, and other diseases. An institution that evolved from the Scripps Metabolic Clinic founded by philanthropist Ellen Browning Scripps in 1924, the institute now employs about 3,000 people on its campuses in La Jolla, CA, and Jupiter, FL, where its renowned scientists including three Nobel laureates work toward their next discoveries. The institutes graduate program, which awards PhD degrees in biology and chemistry, ranks among the top ten of its kind in the nation. For more information, see www.scripps.edu.

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