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

被引:8
|
作者
Nothisen, Marc
Bagilet, Jeremy
Behr, Jean-Paul
Remy, Jean-Serge [1 ]
Kotera, Mitsuharu [1 ]
机构
[1] Univ Strasbourg, Lab V SAT, CAMB, UMR 7199, F-67401 Illkirch Graffenstaden, France
关键词
cationic oligospermine-siRNA conjugate; chemically modified siRNA; carrier-free transfection; siRNA delivery; NUCLEIC-ACID THERAPEUTICS; RNAI THERAPEUTICS; MAMMALIAN-CELLS; CHEMICAL-MODIFICATIONS; TARGETED DELIVERY; INTERFERENCE; ANTISENSE; DUPLEXES; OLIGONUCLEOTIDES; HYBRIDIZATION;
D O I
10.1021/acs.molpharmaceut.6b00309
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:2718 / 2728
页数:11
相关论文
共 50 条
  • [1] Cationic Oligospermine-Oligonucleotide Conjugates Provide Carrier-free Splice Switching in Monolayer Cells and Spheroids
    Nothisen, Marc
    Perche-Letuvee, Phanelie
    Behr, Jean-Paul
    Remy, Jean-Serge
    Kotera, Mitsuharu
    [J]. MOLECULAR THERAPY-NUCLEIC ACIDS, 2018, 13 : 483 - 492
  • [2] Cationic siRNAs Provide Carrier-Free Gene Silencing in Animal Cells
    Nothisen, Marc
    Kotera, Mitsuharu
    Voirin, Emilie
    Remy, Jean-Serge
    Behr, Jean-Paul
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (49) : 17730 - 17731
  • [3] Carrier-free Gene Silencing by Amphiphilic Nucleic Acid Conjugates in Differentiated Intestinal Cells
    Moroz, Elena
    Lee, Soo Hyeon
    Yamada, Ken
    Halloy, Francols
    Martinez-Montero, Saul
    Jahns, Hartmut
    Hall, Jonathan
    Damha, Masad J.
    Castagner, Bastien
    Leroux, Jean-Christophe
    [J]. MOLECULAR THERAPY-NUCLEIC ACIDS, 2016, 5 : e364
  • [4] Lipophilic siRNA targets albumin in situ and promotes bioavailability, tumor penetration, and carrier-free gene silencing
    Sarett, Samantha M.
    Werfel, Thomas A.
    Lee, Linus
    Jackson, Meredith A.
    Kilchrist, Kameron V.
    Brantley-Sieders, Dana
    Duvall, Craig L.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (32) : E6490 - E6497
  • [5] Effective carrier-free gene-silencing activity of sphingosine-modified siRNAs
    Fernandez, Charlene
    Giorgees, Ifrodet
    Goss, Eva
    Desaulniers, Jean-Paul
    [J]. ORGANIC & BIOMOLECULAR CHEMISTRY, 2023, 21 (10) : 2107 - 2117
  • [6] Effective carrier-free gene-silencing activity of cholesterol-modified siRNAs
    Salim, Lidya
    McKim, Chris
    Desaulniers, Jean-Paul
    [J]. RSC ADVANCES, 2018, 8 (41): : 22963 - 22966
  • [7] Carrier-free cellular uptake and the gene-silencing activity of the lipophilic siRNAs is strongly affected by the length of the linker between siRNA and lipophilic group
    Petrova, Natalya S.
    Chernikov, Ivan V.
    Meschaninova, Mariya I.
    Dovydenko, Iiya S.
    Venyaminova, Aliya G.
    Zenkova, Marina A.
    Vlassov, Valentin V.
    Chernolovskaya, Elena L.
    [J]. NUCLEIC ACIDS RESEARCH, 2012, 40 (05) : 2330 - 2344
  • [8] Cyclodextrin-siRNA conjugates as versatile gene silencing agents
    Malhotra, Meenakshi
    Gooding, Matt
    Evans, James C.
    O'Driscoll, Daniel
    Darcy, Raphael
    O'Driscoll, Caitriona M.
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 114 : 30 - 37
  • [9] Structure and gene silencing activities of monovalent and pentavalent cationic lipid vectors complexed with siRNA
    Bouxsein, Nathan F.
    McAllister, Christopher S.
    Ewert, Kai K.
    Samuel, Charles E.
    Safinya, Cyrus R.
    [J]. BIOCHEMISTRY, 2007, 46 (16) : 4785 - 4792
  • [10] Hyaluronic acid-siRNA conjugates complexed with cationic solid lipid nanoparticles for target specific gene silencing
    Lee, Min-Young
    Kong, Won Ho
    Jung, Ho Sang
    Hahn, Sei Kwang
    [J]. RSC ADVANCES, 2014, 4 (37): : 19338 - 19344