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Commercial nanopore sequencers are now available. These devices are based on biological nanopores and sequence DNA using ion-current measurements. Nanopores can also be made from synthetic materials, but, at present, these nanopores are less sophisticated and capable than their biological counterparts. However, they allow read-out mechanisms other than ion-current measurements to be exploited and could, in the future, provide cheaper and more versatile devices, with applications in the analysis of DNA, proteins and beyond. In this focus we examine some of the possibilities for advanced synthetic nanopores and highlight the challenges the field faces in delivering practical devices.
Sophisticated nanopores, which utilize electron tunnelling measurements, two-dimensional materials, or concepts from molecular self-assembly, could have applications in DNA and protein sequencing; the technical problems that must be solved to realize such technologies are considerable though.
Nanopores are on the brink of fundamentally changing DNA sequencing. At the same time, DNA origami provides unprecedented freedom in molecular design. Here, I suggest why a combination of solid-state nanopores and DNA nanotechnology will lead to exciting new experiments.
Sequencing methods based on electron tunnelling could lead to breakthroughs in genomics, proteomics and glycomics, but the engineering challenges involved in delivering these devices are formidable.
This article reviews the use of quantum tunnelling for sequencing DNA, RNA and peptides, highlighting the potential advantages of the approach and the significant technical challenges that must be addressed to deliver practical quantum sequencing devices.
This article reviews the use of graphene nanodevices for DNA sequencing, highlighting the potential of approaches that involve DNA molecules passing through graphene nanopores, nanogaps, and nanoribbons, or the physisorption of DNA on graphene nanostructures.