Improving Signal/Noise Resolution in Single-Molecule Experiments Using Molecular Constructs with Short Handles

被引:62
作者
Forns, N. [1 ]
de Lorenzo, S. [6 ]
Manosas, M. [1 ,2 ,3 ,4 ]
Hayashi, K. [5 ]
Huguet, J. M. [1 ]
Ritort, F. [1 ,6 ]
机构
[1] Univ Barcelona, Fac Fis, Dept Fis Fonamental, E-08028 Barcelona, Spain
[2] Ecole Normale Super, Ctr Natl Rech Sci, Unite Mixte Rech 8550, Lab Phys Stat, F-75231 Paris, France
[3] Univ Paris 06, Paris, France
[4] Univ Paris 07, Paris, France
[5] Osaka Univ, Inst Sci & Ind Res, Osaka, Japan
[6] Inst Sanidad Carlos III, CIBER Bioingn Biomat & Nanomed, Madrid, Spain
关键词
FORCE UNFOLDING KINETICS; OPTICAL TWEEZERS; RNA; DNA; ELASTICITY; POLYMER;
D O I
10.1016/j.bpj.2011.01.071
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We investigate unfolding/folding force kinetics in DNA hairpins exhibiting two and three states with newly designed short dsDNA handles (29 bp) using optical tweezers. We show how the higher stiffness of the molecular setup moderately enhances the signal/noise ratio (SNR) in hopping experiments as compared to conventional long-handled constructs (congruent to 700 bp). The shorter construct results in a signal of higher SNR and slower folding/unfolding kinetics, thereby facilitating the detection of otherwise fast structural transitions. A novel analysis, as far as we are aware, of the elastic properties of the molecular setup, based on high-bandwidth measurements of force fluctuations along the folded branch, reveals that the highest SNR that can be achieved with short handles is potentially limited by the marked reduction of the effective persistence length and stretch modulus of the short linker complex.
引用
收藏
页码:1765 / 1774
页数:10
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