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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Hilvert, Donald Torbeev, Vladimir Yu |
| Description | Author Affiliation: Torbeev VY ( Laboratory of Organic Chemistry, ETH Zurich, CH-8093 Zurich, Switzerland.); |
| Abstract | The human protein ß2-microglobulin (ß2m) aggregates as amyloid fibrils in patients undergoing long-term hemodialysis. Isomerization of Pro32 from its native cis to a nonnative trans conformation is thought to trigger ß2m misfolding and subsequent amyloid assembly. To examine this hypothesis, we systematically varied the free-energy profile of proline cis-trans isomerization by replacing Pro32 with a series of 4-fluoroprolines via total chemical synthesis. We show that ß2m's stability, (un)folding, and aggregation properties are all influenced by the rate and equilibrium of Pro32 cis-trans isomerization. As anticipated, the ß2m monomer was either stabilized or destabilized by respective incorporation of (2S,4S)-fluoroproline, which favors the native cis amide bond, or the stereoisomeric (2S,4R)-fluoroproline, which disfavors this conformation. However, substitution of Pro32 with 4,4-difluoroproline, which has nearly the same cis-trans preference as proline but an enhanced isomerization rate, caused pronounced destabilization of the protein and increased oligomerization at neutral pH. More remarkably, these subtle alterations in chemical composition--incorporation of one or two fluorine atoms into a single proline residue in the 99 amino acid long protein--modulated the aggregation properties of ß2m, inducing the formation of polymorphically distinct amyloid fibrils. These results highlight the importance of conformational dynamics for molecular assembly of an amyloid cross-ß structure and provide insights into mechanistic aspects of Pro32 cis-trans isomerism in ß2m aggregation. |
| ISSN | 00278424 |
| e-ISSN | 10916490 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Issue Number | 50 |
| Volume Number | 110 |
| Language | English |
| Publisher | National Academy of Sciences |
| Publisher Date | 2013-12-01 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Amides Chemistry Amyloidosis Prevention & Control Dialysis Adverse Effects Models, Molecular Proline Protein Conformation Beta 2-Microglobulin Biosynthesis Etiology Chromatography, Gel Chromatography, High Pressure Liquid Circular Dichroism Isomerism Magnetic Resonance Spectroscopy Molecular Structure Solubility Research Support, Non-U.S. Gov't Multidisciplinary |
| Content Type | Text |
| Resource Type | Article |
| Subject | Multidisciplinary |
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