Lipid-bilayer-spanning DNA nanopores with a bifunctional porphyrin anchor.
Lipid-bilayer-spanning DNA nanopores with a bifunctional porphyrin anchor.
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DOI:
10.1002/anie.201305765
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发表时间:
2013-11-11
影响因子:
16.6
通讯作者:
Howorka, Stefan
中科院分区:
文献类型:
--
作者:
Burns, Jonathan R.;Goepfrich, Kerstin;Wood, James W.;Thacker, Vivek V.;Stulz, Eugen;Keyser, Ulrich F.;Howorka, Stefan
Chemistry is in a powerful position to enhance the capabilities of DNA nanotechnology.[1, 2] DNA origami offers rationally designed nanoscale structural frameworks,[2, 3] yet chemistry can advance them by adding tailored functionality through the selective modification of nucleic acids with chemical tags. This synergistic approach has helped create new nanoscale devices, ranging from affinity nanoarrays capable of binding proteins [4] and quantum dots,[5] to nanoplatforms for singlemolecule photochemistry,[6] and to molecular display agents for biosensing.[7, 8] Herein, we present a unique chemical strategy for enlarging and enriching the emerging class of membrane-spanning nanopores composed of folded DNA.[9, 10] We show that solely two porphyrin-based hydrophobic tags achieve the otherwise energetically unfavorable anchoring of the highly negatively charged DNA nanostructure into the hydrophobic core of lipid bilayers. This very small number of porphyrin tags considerably simplifies the currently available chemical strategies for bilayer anchoring of nanopores. The aromatic porphyrin tags are also fluorescent, and hence facilitate the microscopic visualization of DNA-based membrane channels. Our generic route for dualfunctional chemical tags can likely be applied to many other DNA designs, and will help broaden experimental access to versatile DNA origami pores.
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影响因子:
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