Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE 19716, USA.
Curr Opin Biotechnol. 2014 Dec;30:211-7. doi: 10.1016/j.copbio.2014.08.001. Epub 2014 Aug 28.
Protein pharmaceutical products are typically active as folded monomers that are composed of one or more protein chains, such as the heavy and light chains in monoclonal antibodies that are a mainstay of current drug pipelines. There are numerous possible aggregated states for a given protein, some of which are potentially useful, while most of which are considered deleterious from the perspective of pharmaceutical product quality and performance. This review provides an overview of how and why different aggregated states of proteins occur, how this potentially impacts product quality and performance, fundamental approaches to control aggregate formation, and the practical approaches that are currently used in the pharmaceutical industry.
蛋白质类药物产品通常以折叠单体的形式存在,这些单体由一条或多条蛋白质链组成,例如单克隆抗体中的重链和轻链,它们是当前药物研发管线的主要组成部分。给定的蛋白质可能存在多种聚集状态,其中一些可能具有潜在的用途,而大多数则被认为从药物产品质量和性能的角度来看是有害的。本文综述了蛋白质发生不同聚集状态的方式和原因、这如何潜在影响产品质量和性能、控制聚集形成的基本方法以及制药行业目前使用的实际方法。