PH- and salt-dependent molecular combing of DNA: experiments and phenomenological model

被引:30
作者
Benke, Annegret [1 ,2 ]
Mertig, Michael
Pompe, Andwolfgang [1 ,2 ]
机构
[1] Tech Univ Dresden, Inst Werkstoffwissensch, D-01062 Dresden, Germany
[2] Tech Univ Dresden, Max Bergmann Zentrum Biomat, D-01062 Dresden, Germany
关键词
SINGLE; POLYELECTROLYTES; ADSORPTION; PARALLEL; BINDING;
D O I
10.1088/0957-4484/22/3/035304
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
lambda-DNA as well as plasmids can be successfully deposited by molecular combing on hydrophobic surfaces, for pH values ranging from 4 to 10. On polydimethylsiloxane (PDMS) substrates, the deposited DNA molecules are overstretched by about 60-100%. There is a significant influence of sodium ions (NaCl) on the surface density of the deposited DNA, with a maximum near to 100 mM NaCl for a DNA solution (28 ng mu l(-1)) at pH 8. The combing process can be described by a micromechanical model including: (i) the adsorption of free moving coiled DNA at the substrate; (ii) the stretching of the coiled DNA by the preceding meniscus; (iii) the relaxation of the deposited DNA to the final length. The sticky ends of lambda-DNA cause an adhesion force in the range of about 400 pN which allows a stable overstretching of the DNA by the preceding meniscus. The exposing of hidden hydrophobic bonds of the overstretched DNA leads to a stable deposition on the hydrophobic substrate. The pH-dependent density of deposited DNA as well as the observed influence of sodium ions can be explained by their screening of the negatively charged DNA backbone and sticky ends, respectively. The final DNA length can be derived from a balance of the stored elastic energy of the overstretched molecules and the energy of adhesion.
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页数:8
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