topSkip to main content

Menu, Secondary

Menu Trigger


Seminal Study Sheds Light on Cell Mitochondria

Cryo-electron microscopy maps of ATP synthase at low pH, in four distinction conformations

STONY BROOK, NY, February 14, 2024 – A collaborative effort led by Stuti Sharma, PhD, Assistant Professor in the Department of Biochemistry & Cell Biology at Stony Brook University, resulted in a promising study toward a better understanding of mitochondrial adenosine triphosphate (ATP) synthase. The work is highlighted in a paper published this month in Nature Structural & Molecular Biology.

Until now, structural studies on the ATP synthase, which is responsible for more than 90 percent of energy production in living cells, had only been conducted at a basic or neutral potential of hydrogen (pH) level.

Mitochondria often turn acidic in cells affected by diseases such as cancer and cardiac ischemia, as these conditions cause body tissues to become oxygen-deficient or hypoxic. Currently, ATP Synthase is a drug target for various infectious diseases, cardiovascular diseases and cancer. For instance, bedaquiline (Sirturo) is an FDA approved drug that targets bacterial ATP synthase and is prescribed against tuberculosis. So, the potential to broaden ATP synthase-targeted drugs may be viable with additional research.

Sharma’s study examined the ATP synthase at an acidic state just below neutral on the pH scale. By examining ATP synthase in this way, the researchers uncovered several new insights into how the enzyme functions. They found four conformations that occur when the ATP synthase is exposed to an acidic environment. Three of these conformations represent distinct stages in the enzyme’s reaction cycle, with two unique states that have not been described before. The study illuminates how the ATP synthase operates under hypoxic conditions.

“To understand the mechanism of action of drugs or to design drugs that target molecular machines, it is important to elucidate the basic working mechanism of that molecule,” says Sharma. “Our study has improved the understanding of the working mechanism of ATP synthase, especially at low pH.”

She hopes this research is an initial step toward the development of new therapies and treatments for the many diseases in which the ATP synthase is implicated.

For more about Sharma’s lab and current investigations, see this webpage.

This work was done in collaboration with David M. Mueller at the Rosalind Franklin Institute, Chicago and Maofu Liao at the Southern University of Science and Technology in China.

This story was originally published by Stony Brook University on February 14, 2024.