Study of PNA-DNA hybridization by AFM-based single-molecule force spectroscopy

被引:12
作者
Cao, Meiwen [1 ]
Deng, Li
Xu, Hai
机构
[1] China Univ Petr East China, Coll Chem Engn, Ctr Bioengn & Biotechnol, Qingdao 266555, Peoples R China
基金
中国国家自然科学基金;
关键词
Peptide nucleic acids; PNA-DNA hybridization; Single-molecule force spectroscopy rupture force; PEPTIDE NUCLEIC-ACIDS; MICROSCOPY; RECOGNITION; ANTIBODY; BINDING; OLIGONUCLEOTIDES; STABILITY; MECHANICS; STRENGTH; STRANDS;
D O I
10.1016/j.colsurfa.2015.01.063
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The PNA-DNA interaction was probed with single-molecule AFM force measurements. The PNA sequence with only six thymine bases, p(T)(6), could form stable hybrids with the complementary DNA sequence of d(A)(6). Rupture of the p(T)(6)-d(A)(6) hybrids required forces of around 148 pN, which was larger than the forces to unbind short DNA duplex that were usually below 100 pN. Fitting into the rupture force-loading rate correlation produced kinetic parameters that describe the PNA-DNA interaction, which were the thermal force scale (f(beta)) to be 17.5 pN, the distance to the energy barrier for dissociation (Delta x) to be 0.23 nm, and the dissociation rate constant at zero force (k(off)) to be 2.5 s(-1), respectively. The results highlighted the stronger binding affinity between PNA and DNA than between DNA and DNA. And by changing the DNA sequence to d(AAGAAA) with a single-base mismatch, no specific rupture events were observed, confirming the high sensitivity of PNA-DNA hybridization to base mismatch. This single-molecule force study probes into the energetic and kinetic aspects of PNA-DNA interactions that are not accessible by conventional bulk methods, leading to deeper understanding of PNA-DNA interactions. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 51
页数:6
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