Department of Chemistry and the Smalley-Curl Institute, Rice University, Houston, Texas 77005, United States.
Department of Materials Science and NanoEngineering, Rice University, Houston, Texas 77005, United States.
J Phys Chem Lett. 2022 Mar 10;13(9):2231-2236. doi: 10.1021/acs.jpclett.2c00030. Epub 2022 Mar 3.
Understanding the conformations of physisorbed single-stranded DNA (ssDNA) oligos on single-wall carbon nanotube (SWCNT) surfaces is important for advancing basic nanoscience and for developing applications in biomedicine and quantum information processing. Here we report evidence that the ssDNA strands are partly desorbed from the nanotube surface under common conditions. SWCNT suspensions were prepared in eight ssDNA oligos, each containing 1 guanine and 30 thymine bases but differing in the position of the guanine within the strand. Singlet oxygen exposure then covalently functionalized the guanine to the SWCNT surface, red-shifting the nanotube fluorescence by an amount reflecting the guanine spatial density at the surface. Spectral shifts were greatest for central guanine positions and smallest for end positions. In conjunction with steered molecular dynamics simulations, the results suggest that steric interference between neighboring ssDNA strands on an individual nanotube causes significant dislocation or desorption of the strand ends while central regions remain better wrapped around the nanotube. This effect decreases with decreasing concentrations of free ssDNA.
了解物理吸附在单壁碳纳米管 (SWCNT) 表面上的单链 DNA (ssDNA) 寡核苷酸的构象对于推进基础纳米科学以及开发在生物医学和量子信息处理中的应用都非常重要。在这里,我们报告了证据表明,ssDNA 链在常见条件下会部分从纳米管表面解吸。SWCNT 悬浮液在 8 种 ssDNA 寡核苷酸中制备,每种寡核苷酸都含有 1 个鸟嘌呤和 30 个胸腺嘧啶碱基,但鸟嘌呤在链中的位置不同。然后,单线态氧暴露将鸟嘌呤共价功能化到 SWCNT 表面,使纳米管荧光红移,其程度反映了表面上鸟嘌呤的空间密度。对于中心鸟嘌呤位置,光谱位移最大,对于末端位置,光谱位移最小。与导向分子动力学模拟相结合,结果表明,单个纳米管上相邻 ssDNA 链之间的空间位阻干扰会导致链末端的明显错位或解吸,而中心区域则更好地包裹在纳米管周围。这种效应随着游离 ssDNA 浓度的降低而减小。