Literature DB >> 22309763

Field programmable chemistry: integrated chemical and electronic processing of informational molecules towards electronic chemical cells.

Patrick F Wagler1, Uwe Tangen, Thomas Maeke, John S McCaskill.   

Abstract

The topic addressed is that of combining self-constructing chemical systems with electronic computation to form unconventional embedded computation systems performing complex nano-scale chemical tasks autonomously. The hybrid route to complex programmable chemistry, and ultimately to artificial cells based on novel chemistry, requires a solution of the two-way massively parallel coupling problem between digital electronics and chemical systems. We present a chemical microprocessor technology and show how it can provide a generic programmable platform for complex molecular processing tasks in Field Programmable Chemistry, including steps towards the grand challenge of constructing the first electronic chemical cells. Field programmable chemistry employs a massively parallel field of electrodes, under the control of latched voltages, which are used to modulate chemical activity. We implement such a field programmable chemistry which links to chemistry in rather generic, two-phase microfluidic channel networks that are separated into weakly coupled domains. Electric fields, produced by the high-density array of electrodes embedded in the channel floors, are used to control the transport of chemicals across the hydrodynamic barriers separating domains. In the absence of electric fields, separate microfluidic domains are essentially independent with only slow diffusional interchange of chemicals. Electronic chemical cells, based on chemical microprocessors, exploit a spatially resolved sandwich structure in which the electronic and chemical systems are locally coupled through homogeneous fine-grained actuation and sensor networks and play symmetric and complementary roles. We describe how these systems are fabricated, experimentally test their basic functionality, simulate their potential (e.g. for feed forward digital electrophoretic (FFDE) separation) and outline the application to building electronic chemical cells.
Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.

Mesh:

Year:  2012        PMID: 22309763     DOI: 10.1016/j.biosystems.2012.01.005

Source DB:  PubMed          Journal:  Biosystems        ISSN: 0303-2647            Impact factor:   1.973


  5 in total

1.  DNA-library assembly programmed by on-demand nano-liter droplets from a custom microfluidic chip.

Authors:  Uwe Tangen; Gabriel Antonio S Minero; Abhishek Sharma; Patrick F Wagler; Rafael Cohen; Ofir Raz; Tzipy Marx; Tuval Ben-Yehezkel; John S McCaskill
Journal:  Biomicrofluidics       Date:  2015-07-08       Impact factor: 2.800

2.  On demand nanoliter-scale microfluidic droplet generation, injection, and mixing using a passive microfluidic device.

Authors:  Uwe Tangen; Abhishek Sharma; Patrick Wagler; John S McCaskill
Journal:  Biomicrofluidics       Date:  2015-02-12       Impact factor: 2.800

3.  Programming chemistry in DNA-addressable bioreactors.

Authors:  Harold Fellermann; Luca Cardelli
Journal:  J R Soc Interface       Date:  2014-10-06       Impact factor: 4.118

4.  The MATCHIT automaton: exploiting compartmentalization for the synthesis of branched polymers.

Authors:  Mathias S Weyland; Harold Fellermann; Maik Hadorn; Daniel Sorek; Doron Lancet; Steen Rasmussen; Rudolf M Füchslin
Journal:  Comput Math Methods Med       Date:  2013-12-31       Impact factor: 2.238

5.  Addressing, amplifying and switching DNAzyme functions by electrochemically-triggered release of metal ions.

Authors:  Lina Freage; Alexander Trifonov; Ran Tel-Vered; Eyal Golub; Fuan Wang; John S McCaskill; Itamar Willner
Journal:  Chem Sci       Date:  2015-04-08       Impact factor: 9.825

  5 in total

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