Effect of Nanoparticle Conjugation on Gene Silencing by RNA Interference
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作者:
Singh, Neetu
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MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USAMIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
Singh, Neetu
[1
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Agrawal, Amit
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MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USAMIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
Agrawal, Amit
[1
]
Leung, Anthony K. L.
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MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USAMIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
Leung, Anthony K. L.
[2
]
Sharp, Phillip A.
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MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
MIT, Dept Biol, Cambridge, MA 02139 USAMIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
Sharp, Phillip A.
[2
,3
]
Bhatia, Sangeeta N.
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MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
Brigham & Womens Hosp, Div Med, Boston, MA 02115 USA
MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USAMIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
Bhatia, Sangeeta N.
[1
,2
,4
,5
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机构:
[1] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[2] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
[4] Brigham & Womens Hosp, Div Med, Boston, MA 02115 USA
[5] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
RNA interference (RNAi) is a cellular process whereby the silencing of a particular gene is mediated by short RNAs (siRNAs). Although siRNAs have great therapeutic potential, cellular delivery has been a challenge. Nanoparticle-siRNA conjugates have emerged as potential delivery vehicles; however, reports describing the effects of nanoparticle conjugation on RISC incorporation and subsequent gene silencing have been mixed. In this report, we have systematically evaluated the effect of siRNA coupling strategies using a model nanoparticle system with varying conjugation schemes. We show that the accessibility of the siRNA linked to the nanoparticle and the lability of the cross-linker are critical for efficient gene knockdown.
机构:Univ Calif San Francisco, Programs Human Genet, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
Dong, Zhiqiang
Peng, Jisong
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机构:Univ Calif San Francisco, Programs Human Genet, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
Peng, Jisong
Guo, Su
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Univ Calif San Francisco, Programs Human Genet, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
Univ Calif San Francisco, Program Biol Sci, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USAUniv Calif San Francisco, Programs Human Genet, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA