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Addressable molecular node assembly--functional DNA nanostructures.

John Tumpane (Institutionen för kemi- och bioteknik, Fysikalisk kemi) ; Erik Lundberg (Institutionen för kemi- och bioteknik, Fysikalisk kemi) ; Marcus Wilhelmsson (Institutionen för kemi- och bioteknik, Fysikalisk kemi) ; Tom Brown ; Bengt Nordén (Institutionen för kemi- och bioteknik, Fysikalisk kemi)
Nucleic acids symposium series (2004) (17468272). 52, p. 97-98. (2008)
[Artikel, refereegranskad vetenskaplig]

The use of nucleic acids as a nanomaterial is becoming increasingly widespread due to the suitability of the hydrogen-bonding patterns and sequence specificity inherent to the double-helix. As minimisation of size becomes ever more important it is imperative to employ nucleic acids in the most efficient and functional manner possible. To this end we have constructed DNA nanostructures on what may be the smallest possible scale (basic components of just 10 bp) that not only reliably self-assemble but also where each unit of a 2-dimensional DNA network can be uniquely identified and selectively functionalized.(1,2.3) On this length scale and using full addressability of the network to engrave specific pathways on the scaffold, energy and electron transfer become efficient for potential information storage applications.(4).

Denna post skapades 2017-11-13.
CPL Pubid: 253090


Institutioner (Chalmers)

Institutionen för kemi- och bioteknik, Fysikalisk kemi (2005-2014)



Chalmers infrastruktur