Telethon Kids Institute, University of Western Australia, Subiaco, WA 6008, Australia.
Phylogica Pty Ltd., Subiaco, WA 6008, Australia.
Biomolecules. 2018 Jul 11;8(3):51. doi: 10.3390/biom8030051.
The ability of cell penetrating peptides (CPPs) to deliver biologically relevant cargos into cells is becoming more important as targets in the intracellular space continue to be explored. We have developed two assays based on CPP-dependent, intracellular delivery of TEM-1 β-lactamase enzyme, a functional biological molecule comparable in size to many protein therapeutics. The first assay focuses on the delivery of full-length β-lactamase to evaluate the internalization potential of a CPP sequence. The second assay uses a split-protein system where one component of β-lactamase is constitutively expressed in the cytoplasm of a stable cell line and the other component is delivered by a CPP. The delivery of a split β-lactamase component evaluates the cytosolic delivery capacity of a CPP. We demonstrate that these assays are rapid, flexible and have potential for use with any cell type and CPP sequence. Both assays are validated using canonical and novel CPPs, with limits of detection from <500 nM to 1 µM. Together, the β-lactamase assays provide compatible tools for functional characterization of CPP activity and the delivery of biological cargos into cells.
细胞穿透肽(CPPs)将生物相关有效载荷递送至细胞内的能力正变得越来越重要,因为细胞内空间的靶点不断被探索。我们已经开发了两种基于 CPP 依赖性的细胞内 TEM-1 酶传递的测定方法,该酶是一种功能性生物分子,其大小与许多蛋白治疗药物相当。第一个测定方法专注于全长β-内酰胺酶的传递,以评估 CPP 序列的内化潜力。第二个测定方法使用分裂蛋白系统,其中β-内酰胺酶的一个组成部分在稳定细胞系的细胞质中持续表达,另一个组成部分由 CPP 传递。分裂β-内酰胺酶成分的传递评估 CPP 的胞质递送能力。我们证明这些测定方法快速、灵活,并且具有与任何细胞类型和 CPP 序列一起使用的潜力。使用经典和新型 CPP 对两种测定方法进行了验证,检测限从 <500 nM 到 1 μM。这两种测定方法共同为 CPP 活性的功能特征分析以及生物有效载荷的细胞内传递提供了兼容的工具。