期刊
BIOPHYSICAL JOURNAL
卷 96, 期 7, 页码 2926-2934出版社
CELL PRESS
DOI: 10.1016/j.bpj.2008.12.3933
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The most commonly used optical-trapping assays are coupled to surfaces, yet such assays lack atomic-scale (similar to 0.1 nm) spatial resolution due to drift between the surface and trap. We used active stabilization techniques to minimize surface motion to 0.1 nm in three dimensions and decrease multiple types of trap laser noise (pointing, intensity, mode, and polarization). As a result, we achieved nearly the thermal limit (<0.05 nm) of bead detection over abroad range of trap stiffness (k(T) = 0.05-0.5 pN/nm) and frequency (Delta f = 0.03-100 Hz). We next demonstrated sensitivity to one-basepair (0.34-nm) steps along DNA in a surface-coupled assay at moderate force (6 pN). Moreover, basepair stability was achieved immediately after substantial (3.4 pN) changes in force. Active intensity stabilization also led to enhanced force precision (similar to 0.01%) that resolved 0.1-pN force-induced changes in DNA hairpin unfolding dynamics. This work brings the benefit of atomic-scale resolution, currently limited to dual-beam trapping assays, along with enhanced force precision to the widely used, surface-coupled optical-trapping assay.
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