Department of Physics, McGill University, Montreal, QC, Canada.
Proc Natl Acad Sci U S A. 2010 Jul 27;107(30):13294-9. doi: 10.1073/pnas.1007081107. Epub 2010 Jul 7.
Here we explore the potential power of denaturation mapping as a single-molecule technique. By partially denaturing YOYO-1-labeled DNA in nanofluidic channels with a combination of formamide and local heating, we obtain a sequence-dependent "barcode" corresponding to a series of local dips and peaks in the intensity trace along the extended molecule. We demonstrate that this structure arises from the physics of local denaturation: statistical mechanical calculations of sequence-dependent melting probability can predict the barcode to be observed experimentally for a given sequence. Consequently, the technique is sensitive to sequence variation without requiring enzymatic labeling or a restriction step. This technique may serve as the basis for a new mapping technology ideally suited for investigating the long-range structure of entire genomes extracted from single cells.
在这里,我们探索了部分变性作图作为一种单分子技术的潜在能力。通过在纳米流道中使用甲酰胺和局部加热对 YOYO-1 标记的 DNA 进行部分变性,我们得到了一个与延伸分子上强度轨迹中一系列局部下降和上升相对应的序列依赖性“条码”。我们证明,这种结构源于局部变性的物理性质:序列依赖性熔解概率的统计力学计算可以预测在给定序列下实验中观察到的条码。因此,该技术对序列变化敏感,而不需要酶标记或限制步骤。该技术可以作为一种新的作图技术的基础,非常适合研究从单个细胞中提取的整个基因组的长程结构。