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DNA 扭曲的能量学。II. 拓扑异构体分析。

Energetics of DNA twisting. II. Topoisomer analysis.

作者信息

Shore D, Baldwin R L

出版信息

J Mol Biol. 1983 Nov 15;170(4):983-1007. doi: 10.1016/s0022-2836(83)80199-5.

Abstract

A gel electrophoresis method has been developed for resolving small (approximately equal to 250 bp DNA topoisomers. In this size range only one major topoisomer band is observed, except for ligase closure conditions in which the probabilities are nearly equal for circularization by untwisting and overtwisting the corresponding linear DNA. The two probabilities are nearly equal when delta Tw is close to 0.5, if the mean helical twist of the linear DNA is n + delta Tw, where n is an integer and delta Tw is the fractional twist. We determine delta Tw of the linear DNA in standard conditions (20 degrees C, no ethidium) by titration experiments in which delta Tw is varied at the time of ligase closure, either by changing temperature or ethidium concentration. The endpoint (delta Tw = 0.5) is found when the two topoisomers formed by untwisting and overtwisting are present at equal concentrations. This analysis assumes that the net writhe is zero and the DNA helix is isotropically bendable. The results confirm the analysis of cyclization probabilities given in the preceding paper: delta Tw = 0 at the two maxima in the curve of j-factor versus DNA length and delta Tw = 0.5 at the minimum. Consequently, we can determine the DNA lengths at which Tw takes on integral values and use them to measure precisely the average helix repeat. From the difference between the delta Tw values of DNAs with 237 and 247 bp, we obtain an approximate value for the helix repeat of h = 10.4 +/- 0.1 bp/turn, in good agreement with earlier values found by the band-shift and nuclease-cutting methods. The twist is integral at 250.8 +/- 0.4 bp and from h = 10.4 +/- 0.1 we find n = 24; then 250.8/24 gives h = 10.45 +/- 0.02 bp/turn. The mean linking number (Lk) changes in a stepwise manner as delta Tw is varied for 250 bp DNAs. This result is expected when the free energy of twisting half a turn becomes large compared to thermal fluctuations. In these experiments, it is possible to obtain the mean Tw value from the mean Lk value only when delta Tw = 0.5, and consequently the mean Lk value is not simply related to DNA length for 250 bp DNAs except when delta Tw = 0.5.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

已开发出一种凝胶电泳方法来分离小片段(约250 bp)的DNA拓扑异构体。在这个大小范围内,通常只观察到一条主要的拓扑异构体条带,但在连接酶封闭条件下除外,在该条件下,相应线性DNA通过解旋和过度旋绕进行环化的概率几乎相等。当ΔTw接近0.5时,这两个概率几乎相等,如果线性DNA的平均螺旋扭转是n + ΔTw,其中n是整数,ΔTw是分数扭转。我们通过滴定实验确定标准条件(20℃,无溴化乙锭)下线性DNA的ΔTw,在连接酶封闭时通过改变温度或溴化乙锭浓度来改变ΔTw。当通过解旋和过度旋绕形成的两种拓扑异构体以相等浓度存在时,找到终点(ΔTw = 0.5)。该分析假设净扭曲为零且DNA螺旋是各向同性可弯曲的。结果证实了前文给出的环化概率分析:在j因子与DNA长度的曲线中的两个最大值处ΔTw = 0,在最小值处ΔTw = 0.5(原文有误,应是最大值处)。因此,我们可以确定Tw取整数值时的DNA长度,并使用它们来精确测量平均螺旋重复。从237和247 bp的DNA的ΔTw值之间的差异,我们得到螺旋重复h的近似值为10.4 +/- 0.1 bp/圈,与通过带移和核酸酶切割方法早期得到的值非常一致。在250.8 +/- 0.4 bp处扭转是整数,根据h = 10.4 +/- 0.1我们得到n = 24;然后250.8/24得出h = 10.45 +/- 0.02 bp/圈。对于250 bp的DNA,随着ΔTw的变化,平均连接数(Lk)以逐步方式变化。当扭转半圈的自由能相对于热涨落变得很大时,这个结果是预期的。在这些实验中,只有当ΔTw = 0.5时,才有可能从平均Lk值获得平均Tw值,因此对于250 bp的DNA,平均Lk值除了在ΔTw = 0.5时外,与DNA长度没有简单的关系。(摘要截短至400字) (原文部分表述有误,已在译文中标注)

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