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Conjugation Approaches for Peptide-Mediated Delivery of Oligonucleotides Therapeutics
被引:7
|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.
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页码:24 / 33
页数:10
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