He Jiaxi, Xu Songhui, Mixson A James
Department of Pathology, University Maryland School of Medicine, 10 S. Pine St., University of Maryland, Baltimore, MD 21201, USA.
Pharmaceutics. 2020 Aug 14;12(8):774. doi: 10.3390/pharmaceutics12080774.
Histidines incorporated into carriers of nucleic acids may enhance the extracellular stability of the nanoparticle, yet aid in the intracellular disruption of the nanoparticle, enabling the release of the nucleic acid. Moreover, protonation of histidines in the endosomes may result in endosomal swelling with subsequent lysis. These properties of histidine are based on its five-member imidazole ring in which the two nitrogen atoms may form hydrogen bonds or act as a base in acidic environments. A wide variety of carriers have integrated histidines or histidine-rich domains, which include peptides, polyethylenimine, polysaccharides, platform delivery systems, viral phages, mesoporous silica particles, and liposomes. Histidine-rich carriers have played key roles in our understanding of the stability of nanocarriers and the escape of the nucleic acids from endosomes. These carriers show great promise and offer marked potential in delivering plasmids, siRNA, and mRNA to their intracellular targets.
掺入核酸载体中的组氨酸可增强纳米颗粒的细胞外稳定性,但有助于纳米颗粒在细胞内的破坏,从而使核酸得以释放。此外,内体中组氨酸的质子化可能导致内体肿胀并随后裂解。组氨酸的这些特性基于其五元咪唑环,其中两个氮原子可形成氢键或在酸性环境中充当碱。多种载体已整合了组氨酸或富含组氨酸的结构域,包括肽、聚乙烯亚胺、多糖、平台递送系统、病毒噬菌体、介孔二氧化硅颗粒和脂质体。富含组氨酸的载体在我们对纳米载体稳定性以及核酸从内体逃逸的理解中发挥了关键作用。这些载体在将质粒、小干扰RNA和信使核糖核酸递送至细胞内靶点方面显示出巨大的前景和显著的潜力。