Newswise — Scientists at The Scripps Research Institute have discovered that certain chemical chaperones help increase the activity of various types of glucocerebrosidase, the enzyme lacking in patients with Gaucher (go-SHAY) disease. This discovery suggests that the active levels of glucocerebrosidase can be improved through the use of select site-directed small molecules or chemical chaperones, which bind and stabilize proteins and prevent their degradation. These findings could lead to the development of first-in-class drugs for the treatment of the disease.
The new study, published in the current issue of Chemical Biology, was led by Jeffery W. Kelly, Ph.D. Kelly is the Lita Annenberg Hazen Professor of Chemistry, a member of The Skaggs Institute for Chemical Biology, and vice president of academic affairs at Scripps Research. He conducted the research with a team of Scripps Research scientists including Anu R. Sawkar, Sara L. Adamski-Werner, Wei-Chieh Cheng, Chi-Huey Wong of the Department of Chemistry and The Skaggs Institute for Chemical Biology; Ernest Beutler of the Department of Molecular and Experimental Medicine; and Klaus-Peter Zimmer of the Universitätskinderklinik, Munster, Germany.
First identified in 1882, Gaucher disease is the most common lipid-storage disorder, the result of a genetic mutation passed from both parents. It is the most common genetic disease among the Ashkenazi Jewish population of Eastern European ancestry. The lack of the specific enzyme, glucoerebrosidase, which helps cells break down the fat molecule glucocerebroside, produces a buildup of fatty deposits primarily in the spleen, liver, and bone marrow. The most common symptoms of Gaucher disease are liver and spleen enlargement, anemia, and bone pain. In a small number of patients with the disease, however, glucocerebroside also accumulates in the central nervous system, leading to neurological damage.
The primary treatment for Gaucher disease is enzyme replacement therapy, with the deficient enzyme replaced with injections of recombinant enzyme, although the treatment does not alleviate neurological symptoms because protein-based therapy cannot cross the blood brain barrier. A small-molecule-based treatment would have a distinct therapeutic advantage for patients with those symptoms.
In an earlier study, published in a 2002 issue of the journal Proceedings of the National Academy of Sciences, Kelly and his colleagues showed that the small molecule N-(n-nonyl) deoxynojirimycin increased the activity of N370S glucocerebrosidase in patient-derived cells, stabilizing the enzyme within the endoplasmic reticulum (ER), an extensive membrane network within cells that helps with protein synthesis and shape acquisition. This approach enabled proteins to exit the ER and proceed to the lysosome, a compartment within the cell membrane that helps the body break down macromolecules, where the accumulated lipid could be degraded.
This most current study was expanded to include more disease-associated glucocerebrosidase mutants plus additional classes of small molecules. The results show that several classes of these glucocerebrosidase mutants were also amenable to chemical chaperoning and that several, but not all, of the compounds tested were able to increase the activity of various glucocerebrosidase variants.
"The fact that the activity of the most common variant that causes Gaucher disease can be increased by chemical chaperoning, coupled with our observation that several chemical classes have proven to be effective chaperones, provides optimism that long-term efforts could result in new therapeutic entities," Kelly said.
"Enzyme replacement therapy has proven to be safe and effective," he added, "but it would be ideal to have compounds that allow the mutated enzyme to become functional. That has been the overall aim of our research. Although we have approved drugs that slow the accumulation of glucosylceramide (a fat-like molecule) for complex pathologies like Gaucher disease, it's almost always better to have three or four different therapeutic approaches because treatments work differently in individuals with distinct genetic backgrounds."
About The Scripps Research Institute
The Scripps Research Institute, headquartered in La Jolla, California, in 15 buildings on 10 acres overlooking the Pacific Ocean, is one of the world's largest independent, non-profit biomedical research organizations. It stands at the forefront of basic biomedical science that seeks to comprehend the most fundamental processes of life. Scripps Research is internationally recognized for its research into immunology, molecular and cellular biology, chemistry, neurosciences, autoimmune, cardiovascular, and infectious diseases, and synthetic vaccine development. Established in its current configuration in 1961, it employs approximately 3,000 scientists, postdoctoral fellows, scientific and other technicians, doctoral degree graduate students, and administrative and technical support personnel.
Scripps Florida, a 364,000 square-foot, state-of-the-art biomedical research facility, is under construction in Palm Beach County. The facility will focus on basic biomedical science, drug discovery, and technology development. Palm Beach County and the State of Florida have provided start-up economic packages for development, building, staffing, and equipping the campus. Scripps Florida now operates with approximately 150 scientists, technicians, and administrative staff at 40,000 square-foot lab facilities on the Florida Atlantic University campus in Jupiter.
RSS