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使用携带光不稳定基团的寡核苷酸来控制纳米颗粒在表面的沉积和纳米颗粒的结合。

Use of oligonucleotides carrying photolabile groups for the control of the deposition of nanoparticles in surfaces and nanoparticle association.

机构信息

Institute for Research in Biomedicine, Baldiri Reixac 10, Barcelona E-08028, Spain; E-Mail:

出版信息

Int J Mol Sci. 2011;12(10):7238-49. doi: 10.3390/ijms12107238. Epub 2011 Oct 24.

DOI:10.3390/ijms12107238
PMID:22072944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3211035/
Abstract

An oligodeoxynucleotide hairpin containing a photolabile 2-nitrobenzyl group in the loop and terminated with a thiol function was prepared. The photocleavage of such a hairpin on gold yields a surface activated with a single stranded oligonucleotide which can be utilised to direct the assembly of nanoparticles conjugated with a complementary strand. Analysis of photocleaved surfaces gives nanoparticle coverage one order of magnitude higher than nonphotocleaved surfaces. This illustrates the ability of photocleavable hairpins to direct the assembly of nanomaterials on conducting materials. The conjugation of the photocleavable hairpin to a gold nanoparticle allows the observation of intermolecular interactions between hairpins linked in different nanoparticles, by comparing the thermal dissociations of a hairpin-nanoparticle conjugates at 260 nm and 520 nm. We have also shown that it is possible to permanently alter the physiochemical properties of DNA-nanoparticles by the introduction of a photocleavable group. Indeed for the first time it has been shown that by exposure to UV light the disassembly of nanoparticle aggregates can be induced.

摘要

制备了一种含有光解 2-硝基苄基基团的发夹状寡核苷酸,其环中含有一个硫醇功能。在金表面上,这种发夹的光解会产生一个表面,该表面被激活为单链寡核苷酸,可用于指导与互补链连接的纳米粒子的组装。对光解表面的分析表明,纳米粒子的覆盖率比非光解表面高一个数量级。这说明了光解发夹引导纳米材料在导电材料上组装的能力。将光解发夹与金纳米粒子连接,通过比较在 260nm 和 520nm 下发夹-纳米粒子缀合物的热解,观察连接在不同纳米粒子中的发夹之间的分子间相互作用。我们还表明,通过引入光解基团,可以永久改变 DNA-纳米粒子的物理化学性质。事实上,这是首次表明通过暴露于紫外光,可以诱导纳米粒子聚集体的解组装。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/e49b4ca2108a/ijms-12-07238f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/f38d071f9b12/ijms-12-07238f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/eae61545707b/ijms-12-07238f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/c87b9b642cfe/ijms-12-07238f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/25915716b3b1/ijms-12-07238f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/ba3b8dd5acb5/ijms-12-07238f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/56f3b424754b/ijms-12-07238f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/e49b4ca2108a/ijms-12-07238f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/f38d071f9b12/ijms-12-07238f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/eae61545707b/ijms-12-07238f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/c87b9b642cfe/ijms-12-07238f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/25915716b3b1/ijms-12-07238f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/ba3b8dd5acb5/ijms-12-07238f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/56f3b424754b/ijms-12-07238f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58f5/3211035/e49b4ca2108a/ijms-12-07238f7.jpg

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引用本文的文献

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Synthesis of oligonucleotides carrying thiol groups using a simple reagent derived from threoninol.使用一种简单的来源于苏氨酸的试剂合成带有巯基的寡核苷酸。
Molecules. 2012 Aug 24;17(9):10026-45. doi: 10.3390/molecules170910026.

本文引用的文献

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