Department of Chemical Physics and Chemical Research Support, Weizmann Institute of Science, Rehovot 76100, Israel.
J Phys Chem B. 2010 Jul 1;114(25):8581-4. doi: 10.1021/jp104533q.
Toward the construction of double stranded DNA-based biosensors, packing of thiolated double-stranded DNA adsorbed on gold nanoparticles was observed to induce DNA denaturation. The denaturation was investigated as a function of DNA density, nanoparticle surface area, and DNA length. Direct correlation was found between DNA surface coverage and the denaturation. Denaturation occurred only at high densities of adsorbed DNA and was dependent on DNA length and therefore stability, providing guidelines for controlled adsorption of dsDNA on GNPs. Our results invoke a model in which the formation of a thiol-gold bond competes with the free energy associated with the denaturation of two DNA strands. Denaturation vacates space for additional molecules to bind through a thiol-gold bond.
为了构建基于双链 DNA 的生物传感器,观察到吸附在金纳米粒子上的巯基化双链 DNA 的组装会诱导 DNA 变性。变性作为 DNA 密度、纳米粒子表面积和 DNA 长度的函数进行了研究。发现 DNA 表面覆盖率与变性之间存在直接相关性。只有在吸附 DNA 的高密度下才会发生变性,并且与 DNA 长度有关,因此与稳定性有关,为 dsDNA 在 GNPs 上的可控吸附提供了指导。我们的结果提出了一种模型,其中形成硫醇-金键与两条 DNA 链变性相关的自由能竞争。变性为通过硫醇-金键结合的其他分子腾出空间。