Dynamics of single-stranded DNA tethered to a solid

作者：Radiom Milad^*; Paul Mark R; Ducker William A

来源：Nanotechnology, 2016, 27(25): 255701.

DOI：10.1088/0957-4484/27/25/255701

• single molecule force spectroscopy
• atomic force microscopy
• relaxation time
• correlation force spectroscopy
• internal friction
• single-stranded DNA

Tethering is used to deliver specific biological and industrial functions. For example, single-stranded DNA (ssDNA) is tethered to polymerases and long sequences of double-stranded DNA (dsDNA) during replication, and to solids in DNA microarrays. However, tethering ssDNA to a large object limits not only the available ssDNA conformations, but also the range of time-scales over which the mechanical responses of ssDNA are important. In this work we examine the effect of tethering by measurement of the mechanical response of ssDNA that is tethered at each end to two separate atomic force microscope cantilevers in aqueous solution. Thermal motion of the cantilevers drives the ends of the ssDNA chain at frequencies near 2 kHz. The presence of a tethered molecule makes a large difference to the asymmetric cross-correlation of two cantilevers, which enables resolution of the mechanical properties in our experiments. By analysis of the correlated motion of the cantilevers we extract the friction and stiffness of the ssDNA. We find that the measured friction is much larger than the friction that is usually associated with the unencumbered motion of ssDNA. We also find that the measured relaxation time, similar to 30 mu s, is much greater than prior measurements of the free-molecule relaxation time. We attribute the difference to the loss of conformational possibilities as a result of constraining the ends of the ssDNA.

• 出版日期2016-6-24
• 单位美国弗吉尼亚理工大学(Virginia Tech)