Conjugation Approaches for Peptide-Mediated Delivery of Oligonucleotides Therapeutics

被引:8
作者
Patil, Nitin A. [1 ]
机构
[1] Monash Univ, Biomed Discovery Inst, Clayton, Vic 3800, Australia
基金
英国医学研究理事会;
关键词
conjugation; oligonucleotide; peptide; peptide nucleic acids; drug delivery; thiol-maleimide conjugation; click chemistry; 2-cyanoisoicotinamide (CINA) linkage; NUCLEIC-ACIDS PNAS; OXIME BOND FORMATION; IN-VIVO DELIVERY; ANTISENSE OLIGONUCLEOTIDES; EFFICIENT CONJUGATION; GENE-EXPRESSION; DNA; LIGATION; SITE; PROTEINS;
D O I
10.1071/CH21131
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oligonucleotide-based agents are versatile biomolecules that modulate gene expression. The last decade has seen the emergence of oligonucleotide-based tools for biochemical investigations. Importantly, several oligonucleotide-based drugs and vaccines are currently used for various therapeutic applications ranging from anti-inflammatory and anti-viral agents to those used in cardiovascular, ophthalmic, and neuro-muscular disorders. Despite a broad range of applications, achieving efficient oligonucleotide delivery remains a major limitation. A possible solution is to conjugate cell-penetrating peptides with oligonucleotides. This review provides an overview of chemical strategies used to synthesise peptide-oligonucleotide conjugates. The merits and liabilities of these strategies are discussed in the context of synthetic efficiency, and bio-reversible and -irreversible linkages.
引用
收藏
页码:24 / 33
页数:10
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