Breakthrough Prize 2020 for biochemist Hartl and geneticist Horwich
Proteins are small molecular machines within each cell and take over a variety of tasks. In order to perform these tasks, newly produced immature chain-like proteins have to fold into a specific, three-dimensional structure. In the 1980s, Hartl and colleagues, in collaboration with Horwich, demonstrated that most of the proteins do not fold spontaneously. Rather, they need assistance in their folding process by so-called molecular chaperones. At the time, this finding contradicted the general dogma. The scientists discovered that certain chaperones are cage-like ‘folding machines’. They offer a protected environment to newly produced proteins, allowing them to fold into their correct functional structure.
Misfolded proteins clump together to form toxic aggregates and are one of the main causes of severe neurodegenerative disorders such as Alzheimer’s disease or Parkinson’s disease. Furthermore, protein misfolding plays an essential role in aging. The findings on chaperone functions make a significant contribution to the development of new therapeutic strategies.
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