Kristensen Mie, Birch Ditlev, Mørck Nielsen Hanne
Section for Biologics, Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark.
Int J Mol Sci. 2016 Jan 30;17(2):185. doi: 10.3390/ijms17020185.
The hydrophilic nature of peptides and proteins renders them impermeable to cell membranes. Thus, in order to successfully deliver peptide and protein-based therapeutics across the plasma membrane or epithelial and endothelial barriers, a permeation enhancing strategy must be employed. Cell-penetrating peptides (CPPs) constitute a promising tool and have shown applications for peptide and protein delivery into cells as well as across various epithelia and the blood-brain barrier (BBB). CPP-mediated delivery of peptides and proteins may be pursued via covalent conjugation of the CPP to the cargo peptide or protein or via physical complexation obtained by simple bulk-mixing of the CPP with its cargo. Both approaches have their pros and cons, and which is the better choice likely relates to the physicochemical properties of the CPP and its cargo as well as the route of administration, the specific barrier and the target cell. Besides the physical barrier, a metabolic barrier must be taken into consideration when applying peptide-based delivery vectors, such as the CPPs, and stability-enhancing strategies are commonly employed to prolong the CPP half-life. The mechanisms by which CPPs translocate cell membranes are believed to involve both endocytosis and direct translocation, but are still widely investigated and discussed. The fact that multiple factors influence the mechanisms responsible for cellular CPP internalization and the lack of sensitive methods for detection of the CPP, and in some cases the cargo, further complicates the design and conduction of conclusive mechanistic studies.
肽和蛋白质的亲水性使其无法透过细胞膜。因此,为了成功地将基于肽和蛋白质的治疗药物递送至质膜、上皮屏障和内皮屏障,必须采用渗透增强策略。细胞穿透肽(CPP)是一种很有前景的工具,已显示出可用于将肽和蛋白质递送至细胞内以及穿过各种上皮组织和血脑屏障(BBB)。通过将CPP与货物肽或蛋白质共价偶联,或通过将CPP与其货物简单大量混合获得物理复合物,均可实现CPP介导的肽和蛋白质递送。这两种方法都有其优缺点,哪种方法是更好的选择可能与CPP及其货物的物理化学性质、给药途径、特定屏障和靶细胞有关。除了物理屏障外,在应用基于肽的递送载体(如CPP)时还必须考虑代谢屏障,通常采用稳定性增强策略来延长CPP的半衰期。据信CPP转运细胞膜的机制涉及内吞作用和直接转运,但仍在广泛研究和讨论中。多种因素影响细胞摄取CPP的机制,且缺乏检测CPP以及在某些情况下检测货物的灵敏方法,这进一步使确定性机制研究的设计和实施变得复杂。