In this article, the topic of Xiaodong Wang (biochemist) will be addressed, which has gained great relevance in recent years due to its impact on various aspects of society. Xiaodong Wang (biochemist) is a topic that has generated interest worldwide, sparking debates and reflections in different areas. From its origins to the present, Xiaodong Wang (biochemist) has been the subject of study by experts and academics, who have sought to understand its implications and consequences. Through this article, different perspectives on Xiaodong Wang (biochemist) will be explored, as well as its relevance in the current context and its possible implications for the future.
Through the government-sponsored Chinese-US Biochemistry Examination and Application (CUSBEA) program, the biochemistry counterpart to CUSPEA, Wang went to the University of Texas Southwestern Medical Center in 1985 for his PhD.[1] The CUSBEA program was initiated by the biochemist Ray Wu at Cornell University and lasted from 1982 to 1989.[5][6] He graduated in 1991.[4]
Since 2003, Wang has been an investigator at the National Institute of Biological Sciences, Beijing (NIBS). In 2010, he ended all his positions in the United States and returned to China to take up the role of director of NIBS.[7]
Wang co-founded two biotechnology companies: Joyant Pharmaceuticals in 2004 and BeiGene in 2010.[9] He currently chairs the Scientific Advisory Board of BeiGene.[10]
Wang chaired the Science Committee of the Future Science Prize in 2017, and currently sits on the committee.[11]
In 1995, Wang reported a protein in hamsters believed to be the one that cleaved SREBP. However, he also found that the human counterpart of this hamster protein was CPP32, which itself was related to one of the first proteins shown to be involved in initiating apoptosis.[13] The CPP32 protein was officially renamed caspase 3 the following year.[14]
Breakthrough came during Wang's one year at Emory University, when he developed a cell-free, in vitro system that replicated the activation of caspase 3 and the initiation of apoptosis.[3] Using this system, his group characterized the proteins required for starting apoptosis, including cytochrome c,[15]Bcl-2,[16]APAF1,[17] and pro-caspase-9.[18]
In 1997, his group reported the activation steps of apoptosis: Bcl-2 regulates the release of cytochrome c from the mitochondria to the cytosol, then cytochrome c binds to APAF1 and forms a protein complex called the apoptosome. The apoptosome recruits and cleaves procaspase-9 to the active form caspase-9, which in turn cleaves procaspase-3 to the active caspase 3.[18]
Apart from apoptosis, Wang also discovered the necroptosis pathway, which is the programmed form of necrosis and another way that a cellkills itself. He established the role of RIPK3 and the MLKL protein in necroptosis.[19]
^ abc"王晓东博士" (in Chinese). National Institute of Biological Sciences, Beijing. Archived from the original on October 19, 2023. Retrieved October 19, 2023.