Investigation of Fibril Forming Mechanisms of l-Phenylalanine and l-Tyrosine: Microscopic Insight toward Phenylketonuria and Tyrosinemia Type II

J Phys Chem B. 2017 Feb 23;121(7):1533-1543. doi: 10.1021/acs.jpcb.6b12220. Epub 2017 Feb 8.

Abstract

Phenylketonuria and tyrosinemia type II, the two metabolic disorders, are originated due to the complications in metabolism of phenylalanine (Phe) and tyrosine (Tyr), respectively. Several neurological injuries, involving microcephaly, mental retardation, epilepsy, motor disease, and skin problems etc., are the symptoms of these two diseases. It has been reported that toxic amyloid fibrils are formed at high concentrations of Phe and Tyr. Our study indicates that the fibril forming mechanisms of Phe and Tyr are completely different. In the case of Phe, -NH3+ and -COO- groups of neighboring molecules interact via hydrogen bonding and polar interactions. On the other hand, there is no role of - NH3+ group in the fibril forming mechanism of Tyr. In Tyr fibril, the two hydrogen bonding partners are -OH and -COO- groups. In addition, we have also investigated the effect of three lanthanide cations on the fibrillar assemblies of Phe. It has been observed that the efficiencies of three lanthanides to inhibit the fibrillar assemblies of Phe follow the order Tb3+< Sm3+< Eu3+.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crown Ethers / chemistry
  • Europium / chemistry
  • Hydrogen Bonding
  • Kinetics
  • Macromolecular Substances / chemistry*
  • Phenylalanine / chemistry*
  • Phenylketonurias / physiopathology
  • Samarium / chemistry
  • Terbium / chemistry
  • Tyrosine / chemistry*
  • Tyrosinemias / physiopathology

Substances

  • Crown Ethers
  • Macromolecular Substances
  • Terbium
  • Tyrosine
  • Samarium
  • Europium
  • Phenylalanine
  • 18-crown-6