CHING SONG
professor
office location:Li Hua Lou Room 111, Xue Yuan Lu #30， Beijng 100083, China
E-mail:chingsong962005@sas.ustb.edu.cn
Research Interests:1.Nuclear receptor LXR signaling and application.
2.Synthetic biology (PI for iGEM)
Cholesterol metabolism is essential in human physiology and common metabolic diseases. We have been working on cholesterol pathology for 30 years, starting from cloning the cholesterol sensor nuclear receptor LXR. It has been increasingly evident that modulation of LXR activity is effective to deccelerate cholesterol accumulation in vascular systems and neurological tissues and slow down the pathological progression of vascular diseases to prevent heart attack and stroke. Diabetes and Alzheimer's disease may also be therapeutically targeted by LXR signaling pathway. In addition to dissect out molecular detail of LXR signaling pathway, synthetic biology method is applied to generate an accelerated aging process where mitochondria is producing ROS is situ under command. A light-powered proton pump is constructed in the inner membrane of mitochondira of cultured human cells. This platform will provide new insight of oxidation hypothesis of aging.
2.Synthetic biology (PI for iGEM)
Cholesterol metabolism is essential in human physiology and common metabolic diseases. We have been working on cholesterol pathology for 30 years, starting from cloning the cholesterol sensor nuclear receptor LXR. It has been increasingly evident that modulation of LXR activity is effective to deccelerate cholesterol accumulation in vascular systems and neurological tissues and slow down the pathological progression of vascular diseases to prevent heart attack and stroke. Diabetes and Alzheimer's disease may also be therapeutically targeted by LXR signaling pathway. In addition to dissect out molecular detail of LXR signaling pathway, synthetic biology method is applied to generate an accelerated aging process where mitochondria is producing ROS is situ under command. A light-powered proton pump is constructed in the inner membrane of mitochondira of cultured human cells. This platform will provide new insight of oxidation hypothesis of aging.
Resume
2005-present professor, USTB
1998-2005 Research Associate University of Chicago US
1994-1996 Senior Scientist, Glaxo Research Institute, US
1989-1994 Ph.D candicate in Bicheistry and Molecular Biology, University of Chicago, US
1984-1988 Undergradaute student in Biology Department, Peking University
Scientific research achievements
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Enrollment plan
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Representative papers
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Postgraduate training
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