共 65 条
Autotransfecting Short Interfering RNA through Facile Covalent Polymer Escorts
被引:40
作者:

Averick, Saadyah E.
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h-index: 0
机构:
Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA

Paredes, Eduardo
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h-index: 0
机构:
Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
Carnegie Mellon Univ, Ctr Nucle Acids Sci & Technol, Pittsburgh, PA 15213 USA Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA

Dey, Sourav K.
论文数: 0 引用数: 0
h-index: 0
机构:
Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
Carnegie Mellon Univ, Ctr Nucle Acids Sci & Technol, Pittsburgh, PA 15213 USA Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA

Snyder, Kristin M.
论文数: 0 引用数: 0
h-index: 0
机构:
Weis Ctr Res, Geisinger Clin, Mol Neurosci Lab, Danville, PA 17822 USA Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA

Tapinos, Nikos
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h-index: 0
机构:
Weis Ctr Res, Geisinger Clin, Mol Neurosci Lab, Danville, PA 17822 USA Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA

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Das, Subha R.
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h-index: 0
机构:
Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
Carnegie Mellon Univ, Ctr Nucle Acids Sci & Technol, Pittsburgh, PA 15213 USA Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
机构:
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Ctr Nucle Acids Sci & Technol, Pittsburgh, PA 15213 USA
[3] Weis Ctr Res, Geisinger Clin, Mol Neurosci Lab, Danville, PA 17822 USA
基金:
美国国家科学基金会;
关键词:
IN-VIVO DELIVERY;
SIRNA DELIVERY;
STAR POLYMERS;
CLICK CHEMISTRY;
PRIMARY-CELLS;
NANOPARTICLES;
CONJUGATION;
OPTIMIZATION;
CANCER;
CORE;
D O I:
10.1021/ja404520j
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Short interfering ribonucleic adds (siRNAs) are important agents for RNA interference (RNAi) that have proven useful in gene function studies and therapeutic applications. However, the efficacy of exogenous siRNAs for gene knockdown remains hampered by their susceptibility to cellular nucleases and impermeability to cell membranes. We report here new covalent polymer-escort siRNA constructs that address both of these constraints simultaneously. By simple postsynthetic click conjugation of polymers to the passenger strand of an siRNA duplex followed by annealing with the complementary guide strand, we obtained siRNA in which one strand includes terminal polymer escorts. The polymer escorts both confer protection against nucleases and facilitate cellular internalization of the siRNA. These autotransfecting polymer-escort siRNAs are viable in RNAi and effective in knocking down reporter and endogenous genes.
引用
收藏
页码:12508 / 12511
页数:4
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