Lopes Raquel R, Tomé Catarina S, Russo Roberto, Paterna Roberta, Leandro João, Candeias Nuno R, Gonçalves Lídia M D, Teixeira Miguel, Sousa Pedro M F, Guedes Rita C, Vicente João B, Gois Pedro M P, Leandro Paula
Research Institute for Medicines, Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.
Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Av. da República, 2780-157 Oeiras, Portugal.
Biomolecules. 2021 Mar 19;11(3):462. doi: 10.3390/biom11030462.
Phenylketonuria (PKU) is a genetic disease caused by deficient activity of human phenylalanine hydroxylase (hPAH) that, when untreated, can lead to severe psychomotor impairment. Protein misfolding is recognized as the main underlying pathogenic mechanism of PKU. Therefore, the use of stabilizers of protein structure and/or activity is an attractive therapeutic strategy for this condition. Here, we report that 3-hydroxyquinolin-2(1H)-one derivatives can act as protectors of hPAH enzyme activity. Electron paramagnetic resonance spectroscopy demonstrated that the 3-hydroxyquinolin-2(1H)-one compounds affect the coordination of the non-heme ferric center at the enzyme active-site. Moreover, surface plasmon resonance studies showed that these stabilizing compounds can be outcompeted by the natural substrate l-phenylalanine. Two of the designed compounds functionally stabilized hPAH by maintaining protein activity. This effect was observed on the recombinant purified protein and in a cellular model. Besides interacting with the catalytic iron, one of the compounds also binds to the N-terminal regulatory domain, although to a different location from the allosteric l-Phe binding site, as supported by the solution structures obtained by small-angle X-ray scattering.
苯丙酮尿症(PKU)是一种由人类苯丙氨酸羟化酶(hPAH)活性不足引起的遗传疾病,若不进行治疗,可导致严重的精神运动障碍。蛋白质错误折叠被认为是PKU的主要潜在致病机制。因此,使用蛋白质结构和/或活性稳定剂是针对这种病症的一种有吸引力的治疗策略。在此,我们报告3-羟基喹啉-2(1H)-酮衍生物可作为hPAH酶活性的保护剂。电子顺磁共振光谱表明,3-羟基喹啉-2(1H)-酮化合物会影响酶活性位点处非血红素铁中心的配位。此外,表面等离子体共振研究表明,这些稳定化合物会被天然底物L-苯丙氨酸取代。所设计的两种化合物通过维持蛋白质活性在功能上稳定了hPAH。在重组纯化蛋白和细胞模型中均观察到了这种效应。除了与催化铁相互作用外,其中一种化合物还与N端调节结构域结合,尽管其结合位置与别构L-苯丙氨酸结合位点不同,小角X射线散射获得的溶液结构支持了这一点。