February 20, 2019
Johns Hopkins Scientists Created and Screened a Library of 45,000 New Compounds
“Reperfusion injuries are a common complication after surgery, especially in the elderly,” says Liu who oversees a library of thousands of the world’s ever-used medicines banked at the Johns Hopkins Drug Library.
The injury occurs when, after surgery, doctors release clamps on blood vessels and a surge of oxygenated blood flows back into tissues that were temporarily starved of it. The wave of blood can shock the tissues causing inflammation and organ damage. The condition can also happen when clogged arteries are opened after heart attacks and strokes. Currently, there are a number of drugs being studied to treat reperfusion injuries, and some treatments, such as blood thinners and anti-inflammatory drugs, can be mildly effective for certain types of the condition.
To find the new drug, Liu, who co-directs the Cancer Chemical and Structural Biology Program at the Johns Hopkins Kimmel Cancer Center, recalled his postdoctoral training years studying how a drug called rapamycin works. Essentially, it suppresses the immune system and is often prescribed to kidney transplant patients to prevent rejection of their new organs.
“I have always thought that rapamycin had interesting qualities,” says Liu. “It’s very stable and cells can absorb high quantities of it, particularly because of its chemical structure.”
Chemically, rapamycin and another immunosuppressant drug, called FK506, contain a unique scaffold that forms nearly half of a ring. That half of the ring, called the FKBP-binding domain, is nearly identical between the two drugs, and the other half, the so-called effector domain, is unique to each of them. The FKBP-binding domain of the drugs confers a number of advantages, including stability and greater distribution throughout the body. The effector domain is what makes each drug target a different protein to suppress the immune system or inhibit cancer cell growth.
Inspired by the unique chemical architectures of rapamycin and FK506, Liu wondered whether it was possible to build similar ring-shaped molecules by swapping out the effector domain of rapamycin and replacing it with new building blocks to target other proteins involved in human diseases.
To do so, Liu and his team made 45,000 combinations of compounds with a FKBP-binding domain and different effector domains. “We could have made many more combinations, but only had a certain amount of resources to work with,” recalls Liu.
Liu and his team divided the massive pool of 45,000 compounds into 3,000 smaller groups and tested each group for those that blocked a chemical pathway associated with reperfusion injury.
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That pathway is a pump system called equilibrative nucleoside transporter, or ENT, which transports a molecule called adenosine, an important biological messenger, into the cell. Tissues starved for oxygen produce large quantities of adenosine. Adenosine protects cells from damage by connecting with receptors on the surface of cells. To control how much and how long adenosine connects with its receptor, cells can dampen the activity of adenosine by swallowing it into the cell through the ENT transporter. “So the goal is to keep adenosine outside of the cell longer to treat reperfusion injuries,” says Liu.
To keep adenosine outside the cell, the scientists looked for the compounds that blocked ENT activity and kept the most adenosine outside the cells to have its tissue-protective effect for as long as possible. One compound rose to the top of their experiments, and they named it rapadocin.
In laboratory studies of 25 mice, the scientists injected them with rapadocin, removed one of their kidneys and clamped the other for 45 minutes; 24 hours later, they sampled their blood for levels of creatinine and nitrogen, which are markers of reperfusion injury.
The animals given rapadocin had one-third less creatinine (0.4 milligrams per deciliter compared with 0.6 milligrams per deciliter on average) and less than half of nitrogen levels (40 milligrams per deciliter compared with 90 milligrams per deciliter on average) than control mice that were given a drug to cancel the effects of rapadocin.
Currently, rapadocin is being developed by Rapafusyn Pharmaceuticals as a potential treatment for kidney reperfusion injury.
Other scientists involved in this research include Zufeng Guo, Sam Y. Hong, Hanjing Peng, Shridhar Bhat, Brandon Peiffer, Chung-Ming Tse and Zhaoli Sun of Johns Hopkins; Jingxin Wang of The Scripps Research Institute; Shahid Rehan and Ville O. Paavilainen of the University of Helsinki, Finland; Wukun Liu of Nanjing University of Chinese Medicine, China; Manisha Das of the U.S. Food and Drug Administration; Wei Li of the Chinese Academy of Sciences, Shanghai, China; Brett R. Ullman of Rapafusyn Pharmaceuticals; Zlatina Tarmakova and Imogen Coe of Ryerson University, Toronto; and Cordelia Schiene-Fischer and Gunter Fischer of Martin Luther University, Germany.
Under a license agreement between Rapafusyn Pharmaceuticals Inc. and The Johns Hopkins University, Drs. Guo, Peng, Bhat, Sun, Liu, and the University are entitled to royalty distributions related to technology described in the study discussed in this publication. Dr. Liu is also a founder of Rapafusyn Pharmaceuticals Inc. and a member of its scientific advisory board. This arrangement has been reviewed and approved by The Johns Hopkins University in accordance with its conflict of interest policies.