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Determinants of cyclization–decyclization kinetics of short DNA with sticky ends

机译:具有粘性末端的短DNA的环化-环化动力学的决定因素

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摘要

Cyclization of DNA with sticky ends is commonly used to measure DNA bendability as a function of length and sequence, but how its kinetics depend on the rotational positioning of the sticky ends around the helical axis is less clear. Here, we measured cyclization (looping) and decyclization (unlooping) rates ( and ) of DNA with sticky ends over three helical periods (100-130 bp) using single-molecule fluorescence resonance energy transfer (FRET). showed a nontrivial undulation as a function of DNA length whereas showed a clear oscillation with a period close to the helical turn of DNA (∼10.5 bp). The oscillation of was almost completely suppressed in the presence of gaps around the sticky ends. We explain these findings by modeling double-helical DNA as a twisted wormlike chain with a finite width, intrinsic curvature, and stacking interaction between the end base pairs. We also discuss technical issues for converting the FRET-based cyclization/decyclization rates to an equilibrium quantity known as the J factor that is widely used to characterize DNA bending mechanics.
机译:具有粘性末端的DNA的环化通常用于测量DNA的可弯曲性,它是长度和序列的函数,但是其动力学如何取决于粘性末端围绕螺旋轴的旋转位置的方法尚不清楚。在这里,我们使用单分子荧光共振能量转移(FRET)测量了在三个螺旋周期(100-130bp)内具有粘性末端的DNA的环化(环化)和去环化(解环)速率(和)。显示出不平凡的起伏随DNA长度的变化而显示出清晰的振荡,其周期接近DNA的螺旋转角(〜10.5 bp)。在粘性末端周围存在间隙的情况下,几乎可以完全抑制的振荡。我们通过将双螺旋DNA建模为具有有限宽度,固有曲率和末端碱基对之间的堆积相互作用的扭曲蠕虫状链来解释这些发现。我们还将讨论将基于FRET的环化/脱环率转换为称为J因子的平衡量的技术问题,该平衡量广泛用于表征DNA弯曲机理。

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