首页> 外文期刊>ACS applied materials & interfaces >Synergetic Approach for Simple and Rapid Conjugation of Gold Nanoparticles with Oligonucleotides
【24h】

Synergetic Approach for Simple and Rapid Conjugation of Gold Nanoparticles with Oligonucleotides

机译:金纳米粒子与寡核苷酸的简单快速结合的协同方法。

获取原文
获取原文并翻译 | 示例
       

摘要

Attaching thiolated DNA on gold nanoparticles (AuNPs) has been extremely important in nanobiotechnology because DNA—AuNPs combine the programmability and molecular recognition properties of the biopolymers with the optical, thermal, and catalytic properties of the inorganic nanomaterials; However, current standard protocols to attach thiolated DNA on AuNPs involve time-consuming, tedious steps and do not perform well for large AuNPs, thereby greatly restricting applications of DNA—AuNPs. Here we demonstrate a rapid and facile strategy to attach thiolated DNA on AuNPs based on the excellent stabilization effect of mPEG-SH on AuNPs. AuNPs are first protected by mPEG-SH in the presence of Tween 20, which results in excellent stability of AuNPs in high ionic strength environments and extreme pHs. A high concentration of NaCl can be applied to the mixture of DNA and AuNP directly, allowing highly efficient DNA attachment to the AuNP surface by minimizing electrostatic repulsion. The entire DNA loading process can be completed in 1.5 h with only a few simple steps. DNA-loaded AuNPs are stable for more than 2 weeks at room temperature, and they can precisely hybridize with the complementary sequence, which was applied to prepare core—satellite nanostructures. Moreover, cytotoxicity assay confirmed that the DNA-AuNPs synthesized by this method exhibit lower cytotoxicity than those prepared by current standard methods. The proposed method provides a new way to stabilize AuNPs for rapid and facile loading thiolated DNA on AuNPs and will find wide applications in many areas requiring DNA—AuNPs, including diagnosis, therapy, and imaging.
机译:在纳米生物技术中,将硫醇化DNA附着在金纳米颗粒(AuNPs)上极为重要,因为DNA-AuNPs结合了生物聚合物的可编程性和分子识别特性以及无机纳米材料的光学,热和催化特性。但是,当前将硫醇化DNA附着在AuNPs上的标准方案涉及耗时,繁琐的步骤,并且对于大型AuNPs效果不佳,从而极大地限制了DNA-AuNPs的应用。在这里,我们证明了基于mPEG-SH对AuNPs的出色稳定作用,将硫醇化DNA附着在AuNPs上的快速简便的策略。 AuNP首先在Tween 20存在下被mPEG-SH保护,这导致AuNP在高离子强度环境和极端pH值下具有出色的稳定性。可以将高浓度的NaCl直接应用于DNA和AuNP的混合物,从而通过最小化静电排斥力使DNA高效附着到AuNP表面。只需几个简单的步骤,即可在1.5小时内完成整个DNA加载过程。载有DNA的AuNP在室温下稳定超过2周,并且可以与互补序列精确杂交,该序列被用于制备核心-卫星纳米结构。此外,细胞毒性测定证实了通过这种方法合成的DNA-AuNPs显示出比通过当前标准方法制备的DNA-AuNP更低的细胞毒性。拟议的方法提供了一种稳定AuNPs的新方法,以便在AuNPs上快速,轻松地加载硫醇化DNA,并将在需要DNA-AuNPs的许多领域得到广泛应用,包括诊断,治疗和成像。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号