DNA origami-based shape IDs for single-molecule nanomechanical genotyping

Variations on DNA sequences profoundly affect how we develop diseases and respond to pathogens and drugs. Atomic force microscopy (AFM) provides a nanomechanical imaging approach for genetic analysis with nanometre resolution. However, unlike fluorescence imaging that has wavelength-specific fluorop...

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Veröffentlicht in:Nature communications 2017-04, Vol.8 (1), p.14738-7, Article 14738
Hauptverfasser: Zhang, Honglu, Chao, Jie, Pan, Dun, Liu, Huajie, Qiang, Yu, Liu, Ke, Cui, Chengjun, Chen, Jianhua, Huang, Qing, Hu, Jun, Wang, Lianhui, Huang, Wei, Shi, Yongyong, Fan, Chunhai
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Sprache:eng
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Zusammenfassung:Variations on DNA sequences profoundly affect how we develop diseases and respond to pathogens and drugs. Atomic force microscopy (AFM) provides a nanomechanical imaging approach for genetic analysis with nanometre resolution. However, unlike fluorescence imaging that has wavelength-specific fluorophores, the lack of shape-specific labels largely hampers widespread applications of AFM imaging. Here we report the development of a set of differentially shaped, highly hybridizable self-assembled DNA origami nanostructures serving as shape IDs for magnified nanomechanical imaging of single-nucleotide polymorphisms. Using these origami shape IDs, we directly genotype single molecules of human genomic DNA with an ultrahigh resolution of ∼10 nm and the multiplexing ability. Further, we determine three types of disease-associated, long-range haplotypes in samples from the Han Chinese population. Single-molecule analysis allows robust haplotyping even for samples with low labelling efficiency. We expect this generic shape ID-based nanomechanical approach to hold great potential in genetic analysis at the single-molecule level. Atomic force microscopy allows for the imaging of molecules at a nanometre resolution. Here the authors combine AFM with self-assembling DNA origami structures to detect single-nucleotide polymorphisms and determine haplotypes.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms14738