GEL-ELECTROPHORESIS OF AN END-LABELED DNA .1. DYNAMICS AND TRAPPING IN CONSTANT FIELDS

被引:20
作者
DEFONTAINES, AD [1 ]
VIOVY, JL [1 ]
机构
[1] ESPCI, PHYSICOCHIM THEOR LAB, 10 RUE VAUQUELIN, F-75231 PARIS 05, FRANCE
关键词
D O I
10.1002/elps.1150140103
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A theory for the gel electrophoresis of a flexible polyelectrolyte, bearing an uncharged bulky label or an uncharged section at one end, is presented. We first consider a gel that is fully permeable to the label: we calculate the degree of stretching of the polyelectrolyte and its mobility as a function of chain size, electric field and label friction. Various regimes are identified, and their ''existence domains'' are calculated. For increasing friction, we predict a transition from a mobility decreasing with chain size to a mobility increasing with chain size. Secondly, we consider the possibility that the label may get trapped at some locations of the gel, a situation relevant to a method of ''trapping electrophoresis'' recently proposed by Ulanovsky et al. for DNA sequencing. A molecular model for detrapping by thermally activated ''backward reptation'' is constructed and solved using the Kramers rate-equation theory. Different closed analytical expressions and approximate scaling laws corresponding to different regimes of stretching and field strengths are predicted. The most striking result is a mobility which exponentially decreases past a critical size N(p)*, which decreases with increasing field. In the regime relevant to the experiments by Ulanowsky et al., we predict N(p)* approximately E-2/3. The predictions are in good qualitative agreement with presently available experiments, but further experimental investigations are suggested.
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页码:8 / 17
页数:10
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