Anticancer Drugs with Fewer Side-effects: Scientists Decode the Crystal Structure of a Key Cell Cycle Protein
Scientists from Japan reveal the crystal structure of a cell cycle motor protein, which could be a potential anticancer drug candidate
Many anticancer drugs have serious side-effects in clinical practice. Kinesin inhibitors block kinesin motor proteins required for cancer cell division, and are thus, promising anticancer drug candidates with minimal side-effects. However, their association with kinesin proteins remains unclear. Researchers from Japan have now addressed this gap by solving the crystal structure of the complex formed by the kinesin protein CENP-E and the non-hydrolyzable ATP analogue AMPPNP, paving the way for the development of cancer therapies with lesser toxicities.
Anticancer drugs are pivotal to cancer treatment, but their toxicity may not always be limited to cancer cells, resulting in harmful side-effects. To develop anticancer therapies that have fewer adverse effects on patients, scientists are now focusing on molecules that are less toxic to cells. One such group of drugs is the "kinesin inhibitors." These inhibitors prevent cancer progression by explicitly targeting kinesin motor proteins, which are required for the division of cancer cells. Centromere-associated protein E (CENP-E), a member of the kinesin motor protein, is a promising target for inhibitor therapy, as it is essential for tumor cell replication. However, determining the structure of CENP-E is crucial to identify inhibitor molecules that can bind to CENP-E and arrest the function.
Interestingly, the binding of the energy molecule-adenosine triphosphate (ATP)-to the motor domain of CENP-E changes its structure or configuration. This also occurs when CENP-E binds to an inhibitor. So far, very few CENP-E inhibitors have been reported and none have been approved for clinical use. It is, therefore, important to acquire structural information on the CENP-E motor domain.
To this end, a research team from Tokyo University of Science (TUS) in Japan used X-ray crystallography to elucidate the crystal structure of the complex formed by the CENP-E motor domain and a kinesin inhibitor.
The study, which was led by Professor Hideshi Yokoyama from TUS, along with co-authors Ms. Asuka Shibuya from TUS, and Assistant Professor Naohisa Ogo, Associate Professor Jun-ichi Sawada, and Professor Akira Asai from the University of Shizuoka, was published in FEBS Letters on February 23, 2023. "CENP-E selectively acts on dividing cells, making it a potential new target for anticancer drugs with fewer side-effects", says Dr. Yokoyama while discussing the motivation underlying this study.
First, the team expressed the CENP-E motor domain in bacterial cells, following which they purified and mixed it with adenylyl-imidodiphosphate (AMPPNP)-a non-hydrolyzable ATP analogue. The mix was crystallized to obtain exhaustive X-ray data. Using this data, the team obtained the structure of CENP-E motor domain-AMPPNP complex. Next, they compared the structure with that of CENP-E-bound adenosine diphosphate (CENP-E-MgADP) as well as with other previously known kinesin motor protein-AMPPNP complexes. From these comparisons, the team speculated that the helix alpha 4 in the motor domain was likely to be responsible for the loose binding of CENP-E to microtubules, i.e., cell structures that are crucial to cell division.
"Compared to the α4 helices of other kinesins, the α4 of CENP-E binds slowly and with lesser strength to microtubules as compared to other kinesins, throughout the ATP hydrolysis cycle", adds Dr.Yokoyama.
The discovery of the crystal structure of the complex is expected to facilitate additional structure-activity relationship studies, which will bring scientists a step closer to developing anticancer drugs targeting CENP-E. The research team is optimistic about the future applications of their research and are confident that it will be possible to design drugs based on the methods employed in this study. "The ultimate goal is to use the preparation and crystallization methods described in our study for future drug design studies that aim at developing anticancer drugs with fewer side-effects," concludes a hopeful Dr. Yokoyama.
We, too, believe that this study will bring cancer patients new hope and alleviate the side-effects they experience during treatment.
Image title: Crystal structure of human CENP-E motor domain - AMPPNP complex
Image caption: Researchers from Tokyo University of Science unraveled the structure of a complex formed by centromere-associated protein E (CENP-E) motor domain and adenylyl-imidodiphosphate (AMPPNP), a non-hydrolyzable ATP analogue. Understanding this crystal structure could help in the development of promising anticancer drugs with fewer side-effects.
Image credit: Hideshi Yokoyama from Tokyo University of Science, Japan
License type: CC BY 4.0
|Title of original paper||:||Crystal structure of the motor domain of centromere-associated protein E in complex with a non-hydrolysable ATP analogue|
Tokyo University of Science (TUS) is a well-known and respected university, and the largest science-specialized private research university in Japan, with four campuses in central Tokyo and its suburbs and in Hokkaido. Established in 1881, the university has continually contributed to Japan's development in science through inculcating the love for science in researchers, technicians, and educators.
With a mission of "Creating science and technology for the harmonious development of nature, human beings, and society", TUS has undertaken a wide range of research from basic to applied science. TUS has embraced a multidisciplinary approach to research and undertaken intensive study in some of today's most vital fields. TUS is a meritocracy where the best in science is recognized and nurtured. It is the only private university in Japan that has produced a Nobel Prize winner and the only private university in Asia to produce Nobel Prize winners within the natural sciences field.
About Professor Hideshi Yokoyama
from Tokyo University of Science
Dr. Hideshi Yokoyama is a Professor at Tokyo University of Science's Faculty of Pharmaceutical Sciences. He has 23 years of research experience and has contributed to more than 47 scientific articles in reputed journals. His primary research focus is the structural biology of membrane signaling proteins or drug-target proteins using X-ray crystallography. Prof. Yokoyama has also received the Award for Young Scientists in Tokai Branch of Pharmaceutical Society of Japan. He is a visiting professor at Université Paris-Sud in France and has previously worked at the University of Shizuoka, Japan's National Institute of Advanced Industrial Science and Technology, and the Japan Society for the Promotion of Science.
This study was financially supported by the Japan Society for the Promotion of Science. Grant Numbers: 17K07316, 22K06554.