We've updated our Privacy Policy to make it clearer how we use your personal data.

We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Advertisement
Configuration of Key Protein Involved in Obesity May Lead to Better Treatments
News

Configuration of Key Protein Involved in Obesity May Lead to Better Treatments

Configuration of Key Protein Involved in Obesity May Lead to Better Treatments
News

Configuration of Key Protein Involved in Obesity May Lead to Better Treatments

Scientists have determined the structure of a cell receptor that is closely linked to an obesity protein. This may lead to better therapies. Credit: Yekaterina Kadyshevskaya, USC.
Read time:
 

Want a FREE PDF version of This News Story?

Complete the form below and we will email you a PDF version of "Configuration of Key Protein Involved in Obesity May Lead to Better Treatments"

First Name*
Last Name*
Email Address*
Country*
Company Type*
Job Function*
Would you like to receive further email communication from Technology Networks?

Technology Networks Ltd. needs the contact information you provide to us to contact you about our products and services. You may unsubscribe from these communications at any time. For information on how to unsubscribe, as well as our privacy practices and commitment to protecting your privacy, check out our Privacy Policy

A USC-led international team of scientists has found the precise shape of a key player in human metabolism, which could lead the way to better treatments for obesity and other metabolic disease.

For the study, the scientists focused on a protein in the brain, the melanocortin 4 receptor (or MC4R). This receptor helps with regulating the body’s energy balance by controlling how much energy is stored as fat. Mutations in the gene that encodes the MC4R protein are linked to severe childhood obesity and other forms.

Obesity has tripled worldwide since 1975, according to the World Health Organization. More than 40 million children aged 5 and younger are obese, while more than 650 million adults worldwide are.

“A lot of people think obesity is a lifestyle choice,” said Raymond Stevens, a USC Provost Professor and director of the Bridge Institute at the USC Michelson Center for Convergent Bioscience. “That’s just not true in all cases. Some people have mutations of this gene. And if they have mutations of this gene, many cannot control their eating. It’s this receptor causing this issue in the brain.”

Severe obesity is often linked to other health issues. Recent data on coronavirus have shown that adults 65 and older who are severely obese are among the hardest hit by the illness, according to the Centers for Disease Control and Prevention.

Working with the iHuman Institute at ShanghaiTech University and the Life Sciences Institute at the University of Michigan, Stevens was interested in the MC4R as part of a larger effort to elucidate the structures of a class of proteins called G protein-coupled receptors that control many human functions. MC4R is among them.

As Stevens and his team began to tackle the MC4R structure, they looked for the world’s expert in this area and turned to Roger Cone at the University of Michigan Life Sciences Institute for help on the function of this important receptor.

Scientists at the University of Michigan discovered the MC4R and have been studying its biology and pharmacology for more than 25 years. Since then, four drugs have been developed to target melanocortin receptors in humans. The drug setmelanotide targets the MC4R to treat rare forms of syndromic obesity, which affects about 1 out of 1,500 people. However, the drug is not potent enough to treat dietary obesity — a more common form of the disease.

By determining the structure of MC4R, the scientists were able to see how it binds to and interacts with other drug molecules. Knowing how the protein is configured will enable scientists to develop and test new therapies that can more precisely treat obesity.

Stevens and Cone, senior author’s of the study, highlight the findings as an example of the importance and power of international collaboration.

“We were able to contribute our knowledge of the MC4R to help further the structural biology studies,” says Cone. “And key structural findings from the USC and iHuman Institute researchers are helping us answer more questions about how this receptor functions in human metabolism.”

Reference: Yu et al. (2020). Determination of the melanocortin-4 receptor structure identifies Ca2+ as a cofactor for ligand binding. Science. DOI: 10.1126/science.aaz8995.

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

Advertisement