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Dive into the research topics where Erik P. Lundberg is active.

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Featured researches published by Erik P. Lundberg.


Angewandte Chemie | 2011

Soft-Surface DNA Nanotechnology: DNA Constructs Anchored and Aligned to Lipid Membrane†

Karl Börjesson; Erik P. Lundberg; Jakob G. Woller; Bengt Nordén; Bo Albinsson

No strings attached: At least three attachment points are needed to align a two-dimensional DNA nanoconstruct to a soft lipid membrane surface with a porphyrin nucleoside as membrane anchor (see picture). The resulting freely diffusing DNA constructs can be reversibly assembled on the surface thus enabling the possibility of a self-repairing system.


ACS Nano | 2011

Nanofabrication Yields. Hybridization and Click-Fixation of Polycyclic DNA Nanoassemblies

Erik P. Lundberg; Calin Plesa; L. Marcus Wilhelmsson; Per Lincoln; Tom Brown; Bengt Nordén

We demonstrate the stepwise assembly of a fully addressable polycyclic DNA hexagon nanonetwork for the preparation of a four-ring system, one of the biggest networks yet constructed from tripodal building blocks. We find that the yield exhibits a distinct upper level <100%, a fundamental problem of thermodynamic DNA assembly that appears to have been overlooked in the DNA nanotechnology literature. A simplistic model based on a single step-yield parameter y can quantitatively describe the total yield of DNA assemblies in one-pot reactions as Y = y(duplex)(n), with n the number of hybridization steps. Experimental errors introducing deviations from perfect stoichiometry and the thermodynamics of hybridization equilibria contribute to decreasing the value of y(duplex) (on average y = 0.96 for our 10 base pair hybridization). For the four-ring system (n = 31), the total yield is thus less than 30%, which is clearly unsatisfactory if bigger nanoconstructs of this class are to be designed. Therefore, we introduced site-specific click chemistry for making and purifying robust building blocks for future modular constructs of larger assemblies. Although the present yield of this robust module was only about 10%, it demonstrates a first step toward a general fabrication approach. Interestingly, we find that the click yields follow quantitatively a binomial distribution, the predictability of which indicates the usefulness of preparing pools of pure and robust building blocks in this way. The binomial behavior indicates that there is no interference between the six simultaneous click reactions but that step-yield limiting factors such as topological constraints and Cu(I) catalyst concentration are local and independent.


Langmuir | 2013

Controlling and Monitoring Orientation of DNA Nanoconstructs on Lipid Surfaces

Erik P. Lundberg; Bobo Feng; Amir Saeid Mohammadi; L. Marcus Wilhelmsson; Bengt Nordén

Its extraordinary self-assembly property, with potential to form nonperiodic structures with unique addressability, makes DNA ideal for fabrication of advanced nanostructures. We here demonstrate the controllable tethering of a hexagonal DNA nanostructure in two distinct orientations at the lipid bilayer of a liposome functioning as a soft-matter support. With polarized light (linear dichroism) applied to the flow-aligned liposomes, we show that the construct is preferentially in a parallel alignment with the lipid surface when two anchors are attached while with one anchor only a perpendicular orientation is observed.


Nucleic acids symposium series (2004) | 2008

Addressable Molecular Node Assembly – Functional DNA Nanostructures

John Tumpane; Erik P. Lundberg; L. Marcus Wilhelmsson; Tom Brown; Bengt Nordén

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).


Nucleic acids symposium series (2004) | 2008

Addressable Molecular Node Assembly – High Information Density DNA Nanostructures

Erik P. Lundberg; John Tumpane; Ravindra Kumar; Peter Sandin; Nittaya Gale; Iris Nandhakumar; Bo Albinsson; Per Lincoln; L. Marcus Wilhelmsson; Tom Brown; Bengt Nordén

The inherent self-assembly properties of DNA make it ideal in nanotechnology. We present a fully addressable DNA nanostructure with the smallest possible unit cell, a hexagon with a side-length of only 3.4 nm.(2,3) Using novel three-way oligonucleotides, where each side has a unique double-stranded DNA sequence that can be assigned a specific address, we will build a non-repetitive two-dimensional grid.


Nano Letters | 2007

Triplex addressability as a basis for functional DNA nanostructures

John Tumpane; Ravindra Kumar; Erik P. Lundberg; Peter Sandin; Nittaya Gale; Iris Nandhakumar; Bo Albinsson; Per Lincoln; L. Marcus Wilhelmsson; Tom Brown; Bengt Nordén


Chemical Physics Letters | 2007

Addressable high-information-density DNA nanostructures

John Tumpane; Peter Sandin; Ravindra Kumar; Vicki E.C. Powers; Erik P. Lundberg; Nittaya Gale; Piero Baglioni; Jean-Marie Lehn; Bo Albinsson; Per Lincoln; L. Marcus Wilhelmsson; Tom Brown; Bengt Nordén


Chemical Communications | 2010

A new fixation strategy for addressable nano-network building blocks

Erik P. Lundberg; Afaf H. El-Sagheer; Petr Kocalka; L. Marcus Wilhelmsson; Tom Brown; Bengt Nordén


Biophysical Journal | 2010

Fixation of Self-Assembled DNA Nanostructures by Simultaneous Multicenter Click Chemistry

Erik P. Lundberg; Afaf H. El-Sagheer; Petr Kocalka; Marcus Wilhelmsson; Tom Brown; Bengt Nordén


Archive | 2012

Bottom-up Fabrication of Functional DNA Nanostructures

Erik P. Lundberg

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Bengt Nordén

Chalmers University of Technology

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L. Marcus Wilhelmsson

Chalmers University of Technology

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Bo Albinsson

Chalmers University of Technology

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John Tumpane

Chalmers University of Technology

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Per Lincoln

Chalmers University of Technology

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Peter Sandin

Chalmers University of Technology

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Nittaya Gale

University of Southampton

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