Protein aggregation underlies several neurodegenerative diseases such as Alzheimerâ€™s, Huntingtonâ€™s chorea or Parkinsonâ€™s. Scientists at the Max Planck Institute of Biochemistry (MPIB) in Martinsried near Munich, Germany, now discovered a fundamental mechanism which explains how toxic protein aggregation occurs and why it leads to a widespread impairment of essential cellular functions. â€œNot all proteins are affected by aggregationâ€, says Heidi Olzscha, PhD student at the MPIB. â€œEspecially those proteins are susceptible, which possess specific structural characteristics and are involved in important biological processes.â€ (Cell, January 7, 2011)
To fulfill their different functions, proteins have to acquire the correct three-dimensional structure. In other words, polypeptides have to fold first. Molecular chaperones, a diverse group of conserved proteins, have specialized to assist other proteins during their folding. If the chaperones fail, misfolding and aggregation of the newly synthesized and pre-existing proteins might occur. In the worst case, this results then in neurodegenerative diseases, such as Alzheimerâ€™s, Huntingtonâ€™s chorea or Parkinsonâ€™s. Alzheimerâ€™s disease, for example, develops because the A-beta and tau proteins aggregate, which leads to neuronal dysfunction and cell death. According to Alzheimer Forschung Initiative e. V., approximately 1.2 million people suffer from this disease only in Germany. The risk to fall ill grows with increasing age.
Scientists in the Department of Cellular Biochemistry at the Max Planck Institute of Biochemistry, headed by F.-Ulrich Hartl, now established a novel experimental model aimed at elucidating cellular protein misfolding and discovered why the misfolding and aggregation are deleterious for cells. They prepared several artificial aggregating proteins without any biological function and introduced them into cells. These model proteins clumped together, coaggregating many natural proteins and, in that way, disturbing their function. By means of quantitative proteomics, the researchers discovered that the affected proteins share certain structural characteristics which predispose them for the co-aggregation: They are large in size, less hydrophobic and show a significant increase of disorder in their structure.
“These are proteins that have not only many, but also very important functions in the cell”, explains Martin Vabulas. “For instance, they are responsible for the stability of the cytoskeleton, the organization of the chromatin in nucleus, the transcription of DNA to RNA or the synthesis of proteins. Simultaneous disturbance of several of these essential processes is most probably the reason of the cellular break-down. As a consequence, protein misfolding diseases develop.”
Molecular chaperones could possibly prevent this dire scenario. They are able to shield the aggregates, so that the aggregates cannot get in touch with other proteins anymore. The scientists hope that their new insights might help to develop novel therapeutic strategies in the battle against neurodegenerative diseases, especially at the earlier stages, before the irreversible collapse of cellular protein network sets in.
- Full bibliographic informationAmyloid-like Aggregates Sequester Numerous Metastable Proteins
with Essential Cellular Functions
Heidi Olzscha,1,4 Sonya M. Schermann,1,4 Andreas C. Woerner,1 Stefan Pinkert,1 Michael H. Hecht,2 Gian G. Tartaglia,3,5
Michele Vendruscolo,3 Manajit Hayer-Hartl,1,* F. Ulrich Hartl,1,* and R. Martin Vabulas1,*
1Department of Cellular Biochemistry, Max Planck Institute of Biochemistry, Am Klopferspitz 18, D-82159 Martinsried, Germany
2Department of Chemistry, Princeton University, Princeton, NJ 08544, USA
3Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK
4These authors contributed equally to this work
5Present address: Bioinformatics & Genomics Program, CRG Centre for Genomic Regulation, Dr. Aiguader 88, Barcelona 08003, Spain
*Correspondence: email@example.com (M.H-H.), firstname.lastname@example.org (F.U.H.), email@example.com (R.M.V.)