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Improvement of DNA recognition through molecular imprinting: hybrid oligomer imprinted polymeric nanoparticles (oligoMIP NPs)

机译:通过分子印迹改善DNA识别:杂交低聚物印迹聚合物纳米颗粒(oligoMIP NP)

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摘要

High affinity and specific binding are cardinal properties of nucleic acids in relation to their biological function and their role in biotechnology. To this end, structural preorganization of oligonucleotides can significantly improve their binding performance, and numerous examples of this can be found in Nature as well as in artificial systems. Here we describe the production and characterization of hybrid DNA-polymer nanoparticles (oligoMIP NPs) as a system in which we have preorganized the oligonucleotide binding by molecular imprinting technology. Molecularly imprinted polymers (MIPs) are cost-effective "smart" polymeric materials capable of antibody-like detection, but characterized by superior robustness and the ability to work in extreme environmental conditions. Especially in the nanoparticle format, MIPs are dubbed as one of the most suitable alternatives to biological antibodies due to their selective molecular recognition properties, improved binding kinetics as well as size and dispersibility. Nonetheless, there have been very few attempts at DNA imprinting in the past due to structural complexity associated with these templates. By introducing modified thymine bases into the oligonucleotide sequences, which allow establishing covalent bonds between the DNA and the polymer, we demonstrate that such hybrid oligoMIP NPs specifically recognize their target DNA, and that the unique strategy of incorporating the complementary DNA strands as "preorganized selective monomers" improves the recognition properties without affecting the NPs physical properties such as size, shape or dispersibility.
机译:就其生物学功能及其在生物技术中的作用而言,高亲和力和特异性结合是核酸的基本特性。为此,寡核苷酸的结构预组织可以显着改善其结合性能,并且在自然界和人工系统中都可以找到许多这样的例子。在这里,我们将杂交DNA聚合物纳米颗粒(oligoMIP NP)的生产和表征描述为通过分子印迹技术预先组织寡核苷酸结合的系统。分子印迹聚合物(MIP)是具有成本效益的“智能”聚合物材料,能够进行抗体样检测,但具有出色的耐用性和在极端环境条件下工作的能力。尤其是在纳米颗粒形式中,由于MIP的选择性分子识别特性,改进的结合动力学以及尺寸和分散性,它们被称为生物抗体的最合适替代品之一。但是,由于与这些模板相关的结构复杂性,过去很少进行DNA印迹的尝试。通过将修饰的胸腺嘧啶碱基引入寡核苷酸序列,从而允许在DNA和聚合物之间建立共价键,我们证明了这种杂化oligoMIP NP可以特异性识别其靶DNA,并且独特的策略是将互补的DNA链整合为“预组织的选择性单体”可改善识别性能,而不会影响NP的物理性能,例如尺寸,形状或分散性。

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