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治疗性蛋白质和肽的氧化:结构和生物学后果

Oxidation of therapeutic proteins and peptides: structural and biological consequences.

作者信息

Torosantucci Riccardo, Schöneich Christian, Jiskoot Wim

机构信息

Division of Drug Delivery Technology Leiden Academic Centre for Drug Research (LACDR), Leiden University, P.O. Box 9502, 2300 RA, Leiden, The Netherlands.

出版信息

Pharm Res. 2014 Mar;31(3):541-53. doi: 10.1007/s11095-013-1199-9. Epub 2013 Sep 25.

Abstract

Oxidation is a common degradation pathway that affects therapeutic proteins and peptides during production, purification, formulation, transportation, storage and handling of solid and liquid preparations. In the present work we review the scientific literature about structural and biological consequences of protein/peptide oxidation. Representative examples are discussed of specific products whose oxidation has been recently studied, including monoclonal antibodies, calcitonin, granulocyte colony-stimulating factor, growth hormone, insulin, interferon alpha and beta, oxytocin and parathyroid hormone. These examples illustrate that oxidation often leads to modifications of higher-order structures, including aggregate induction, and can generate products that are pharmacokinetically different, biologically less active and/or potentially more immunogenic than their native counterpart. It is therefore crucially important during the pharmaceutical development of therapeutic proteins and peptides to comprehensively characterize oxidation products and evaluate the impact of oxidation-induced structural modifications on the biological properties of the drug.

摘要

氧化是一种常见的降解途径,在治疗性蛋白质和肽的生产、纯化、制剂、运输、储存以及固体和液体制剂的处理过程中会对其产生影响。在本工作中,我们回顾了有关蛋白质/肽氧化的结构和生物学后果的科学文献。讨论了最近研究过氧化作用的特定产品的代表性实例,包括单克隆抗体、降钙素、粒细胞集落刺激因子、生长激素、胰岛素、α和β干扰素、催产素和甲状旁腺激素。这些实例表明,氧化常常导致高阶结构的改变,包括聚集体的诱导形成,并且能够产生在药代动力学上与天然对应物不同、生物学活性较低和/或潜在免疫原性更强的产物。因此,在治疗性蛋白质和肽的药物开发过程中,全面表征氧化产物并评估氧化诱导的结构修饰对药物生物学性质的影响至关重要。

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