Literature DB >> 27398779

Structure Tuning of Cationic Oligospermine-siRNA Conjugates for Carrier-Free Gene Silencing.

Marc Nothisen1, Jérémy Bagilet1, Jean-Paul Behr1, Jean-Serge Remy1, Mitsuharu Kotera1.   

Abstract

Oligospermine-siRNA conjugates are able to induce efficient luciferase gene silencing upon carrier-free transfection. These conjugates are readily accessible by a versatile automated chemistry that we developed using a DMT-spermine phosphoramidite reagent. In this article, we used this chemistry to study a wide range of structural modifications of the oligospermine-siRNA conjugates, i.e., variation of conjugate positions and introduction of chemical modifications to increase nuclease resistance. At first we examined gene silencing activity of a series of siRNA-tris(spermine) conjugates with and without chemical modifications in standard carrier assisted conditions. The three spermine units attached at one of the two ends of the sense strand or at the 3'-end of the antisense strand are compatible with gene silencing activity whereas attachment of spermine units at the 5'-end of the antisense strand abolished the activity. 2'-O-Methylated nucleotides introduced in the sense strand are compatible while not in the antisense strand. Thiophosphate links could be used without activity loss at the 3'-end of both strands and at the 5'-end of the sense strand to conjugate oligospermine. Consequently a series of oligospermine-siRNA conjugates containing 15 to 45 spermines units in various configurations were chosen, prepared, and examined in carrier-free conditions. Attachment of 30 spermine units singly at the 5'-end of the sense strand provides the most potent carrier-free siRNA. Longevity of luciferase gene silencing was studied using oligospermine-siRNA conjugates. Five day long efficiency with more than 80% gene expression knockdown was observed upon transfection without vector. Oligospermine-siRNA conjugates targeting cell-constitutive natural lamin A/C gene were prepared. Efficient gene silencing was observed upon carrier-free transfection of siRNA conjugates containing 20 or 30 spermine residues grafted at the 5'-end of the sense strand.

Entities:  

Keywords:  carrier-free transfection; cationic oligospermine−siRNA conjugate; chemically modified siRNA; siRNA delivery

Mesh:

Substances:

Year:  2016        PMID: 27398779     DOI: 10.1021/acs.molpharmaceut.6b00309

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  5 in total

1.  Synthetic Approaches for Copolymers Containing Nucleic Acids and Analogues: Challenges and Opportunities.

Authors:  Hao Lu; Jiansong Cai; Ke Zhang
Journal:  Polym Chem       Date:  2021-03-29       Impact factor: 5.582

2.  Synthesis of siRNAs incorporated with cationic peptides R8G7 and R8A7 and the effect of the modifications on siRNA properties.

Authors:  Miho Matsubara; Kenji Honda; Koki Ozaki; Ryohei Kajino; Yuri Kakisawa; Yusuke Maeda; Yoshihito Ueno
Journal:  RSC Adv       Date:  2020-09-21       Impact factor: 4.036

Review 3.  Solid-phase supported design of carriers for therapeutic nucleic acid delivery.

Authors:  Ana Krhac Levacic; Stephan Morys; Ernst Wagner
Journal:  Biosci Rep       Date:  2017-10-31       Impact factor: 3.840

4.  Cationic Oligospermine-Oligonucleotide Conjugates Provide Carrier-free Splice Switching in Monolayer Cells and Spheroids.

Authors:  Marc Nothisen; Phanélie Perche-Létuvée; Jean-Paul Behr; Jean-Serge Remy; Mitsuharu Kotera
Journal:  Mol Ther Nucleic Acids       Date:  2018-10-10       Impact factor: 8.886

5.  Enhanced Intercellular Delivery of cRGD-siRNA Conjugates by an Additional Oligospermine Modification.

Authors:  Kosuke Nakamoto; Yukihiro Akao; Yasuhiro Furuichi; Yoshihito Ueno
Journal:  ACS Omega       Date:  2018-07-24
  5 in total

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