Intrinsic property of phenylalanine to trigger protein aggregation and hemolysis has a direct relevance to phenylketonuria
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-10911-z.pdf
Reference42 articles.
1. Blau, N., van Spronsen, F. J. & Levy, H. L. Phenylketonuria. Lancet 376, 1417–1427, doi: 10.1016/S0140-6736(10)60961-0 (2010).
2. Schlegel, G., Scholz, R., Ullrich, K., Santer, R. & Rune, G. M. Phenylketonuria: Direct and indirect effects of phenylalanine. Experimental neurology 281, 28–36, doi: 10.1016/j.expneurol.2016.04.013 (2016).
3. Ruppert, E. S. Hemolytic disease in association with elevation of serum phenylalanine. The Journal of pediatrics 71, 152–153 (1967).
4. Adler-Abramovich, L. et al. Phenylalanine assembly into toxic fibrils suggests amyloid etiology in phenylketonuria. Nature chemical biology 8, 701–706, doi: 10.1038/nchembio.1002 (2012).
5. Mossou, E. et al. The self-assembling zwitterionic form of l-phenylalanine at neutral pH. Acta Crystallographica Section C 70, 326–331, doi: 10.1107/S2053229614002563 (2014).
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