Alves Márcia M S, Leandro Paula, Mertens Haydyn D T, Pereiro Ana B, Archer Margarida
Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa (ITQB NOVA), 2780-157 Oeiras, Portugal.
LAQV, REQUIMTE, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa (FCT NOVA), 2829-516 Caparica, Portugal.
Nanomaterials (Basel). 2022 Mar 8;12(6):893. doi: 10.3390/nano12060893.
Phenylketonuria (PKU) is an autosomal recessive disease caused by deficient activity of human phenylalanine hydroxylase (hPAH), which can lead to neurologic impairments in untreated patients. Although some therapies are already available for PKU, these are not without drawbacks. Enzyme-replacement therapy through the delivery of functional hPAH could be a promising strategy. In this work, biophysical methods were used to evaluate the potential of [N][CFSO], a biocompatible fluorinated ionic liquid (FIL), as a delivery system of hPAH. The results herein presented show that [N][CFSO] spontaneously forms micelles in a solution that can encapsulate hPAH. This FIL has no significant effect on the secondary structure of hPAH and is able to increase its enzymatic activity, despite the negative impact on protein thermostability. The influence of [N][CFSO] on the complex oligomerization equilibrium of hPAH was also assessed.
苯丙酮尿症(PKU)是一种常染色体隐性疾病,由人类苯丙氨酸羟化酶(hPAH)活性不足引起,在未经治疗的患者中可导致神经功能障碍。尽管目前已有一些针对PKU的治疗方法,但这些方法并非没有缺点。通过递送功能性hPAH进行酶替代疗法可能是一种有前景的策略。在这项工作中,采用生物物理方法评估了一种生物相容性氟化离子液体(FIL)[N][CFSO]作为hPAH递送系统的潜力。本文给出的结果表明,[N][CFSO]在溶液中自发形成胶束,能够包裹hPAH。这种FIL对hPAH的二级结构没有显著影响,并且尽管对蛋白质热稳定性有负面影响,但仍能提高其酶活性。还评估了[N][CFSO]对hPAH复杂寡聚化平衡的影响。