STRETCHING OF A SINGLE TETHERED POLYMER IN A UNIFORM-FLOW

被引:517
作者
PERKINS, TT
SMITH, DE
LARSON, RG
CHU, S
机构
[1] STANFORD UNIV, DEPT PHYS, STANFORD, CA 94305 USA
[2] AT&T BELL LABS, MURRAY HILL, NJ 07974 USA
关键词
D O I
10.1126/science.7701345
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The stretching of single, tethered DNA molecules by a flow was directly visualized with fluorescence microscopy. Molecules ranging in length (L) from 22 to 84 micrometers were held stationary against the flow by the optical trapping of a latex microsphere attached to one end. The fractional extension x/L is a universal function of eta vL(0.54+/-0.05), where eta and v are the viscosity and velocity of the flow, respectively. This relation shows that the DNA is not ''free-draining'' (that is, hydrodynamic coupling within the chain is not negligible) even near full extension (similar to 80 percent). This function has the same form over a lone range as the fractional extension versus force applied at the ends of a worm-like chain. For small deformations (<30 percent of full extension), the extension increases with velocity as x similar to v(0.70+/-0.08). The relative size of fluctuations in extension decreases as sigma(x)/x congruent to 0.42 exp(-4.9 x/L). Video images of the fluctuating chain have a cone-like envelope and show as sharp increase in intensity at the free end.
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页码:83 / 87
页数:5
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