Methods for electronic synthesis of polymers
First Claim
1. An electronically controlled method for combinatorial synthesis of a biopolymer, comprising the steps of:
- providing a plurality of reaction locations on a substrate, each reaction location being individually electronically addressable;
providing an attachment layer upon at least some reaction locations;
placing said reaction locations in contact with a solution containing a charged monomer-A;
selectively biasing those locations at which monomer A is to react at an opposite charge to monomer-A, and biasing those locations at which monomer A is not to react at the same charge as monomer-A;
concentrating and reacting monomer A on the specific A locations;
removing unreacted monomer A;
providing said reaction locations in contact with charged monomer B;
selectively biasing those locations for which monomer B is to react at the opposite charge of monomer-B, and biasing those locations at which monomer B is not to react at the same charge as monomer-B;
concentrating and reacting monomer B on the specific B locations;
removing unreacted monomer B, andrepeating the process with monomers until all biopolymer sequences are complete.
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Abstract
A self-addressable, self-assembling microelectronic device is designed and fabricated to actively carry out and control multi-step and multiplex molecular biological reactions in microscopic formats. These reactions include nucleic acid hybridization, antibody/antigen reaction, diagnostics, and biopolymer synthesis. The device can be fabricated using both microlithographic and micro-machining techniques. The device can electronically control the transport and attachment of specific binding entities to specific micro-locations. The specific binding entities include molecular biological molecules such as nucleic acids and polypeptides. The device can subsequently control the transport and reaction of analytes or reactants at the addressed specific micro-locations. The device is able to concentrate analytes and reactants, remove non-specifically bound molecules, provide stringency control for DNA hybridization reactions, and improve the detection of analytes. The device can be electronically replicated.
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Citations
22 Claims
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1. An electronically controlled method for combinatorial synthesis of a biopolymer, comprising the steps of:
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providing a plurality of reaction locations on a substrate, each reaction location being individually electronically addressable; providing an attachment layer upon at least some reaction locations; placing said reaction locations in contact with a solution containing a charged monomer-A; selectively biasing those locations at which monomer A is to react at an opposite charge to monomer-A, and biasing those locations at which monomer A is not to react at the same charge as monomer-A; concentrating and reacting monomer A on the specific A locations; removing unreacted monomer A; providing said reaction locations in contact with charged monomer B; selectively biasing those locations for which monomer B is to react at the opposite charge of monomer-B, and biasing those locations at which monomer B is not to react at the same charge as monomer-B; concentrating and reacting monomer B on the specific B locations; removing unreacted monomer B, and repeating the process with monomers until all biopolymer sequences are complete. - View Dependent Claims (2, 3, 4, 5)
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6. A method for synthesizing a plurality of polymers, the polymers being composed of monomers in selected positions, at a plurality of locations on an active, programmable electronic matrix device, comprising the steps of:
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providing a selected charged reactant on the device adjacent the locations, synthesizing the polymer by selectively; biasing those locations attractive to the charged reactant where the polymer includes a specified monomer at the selected position, and simultaneously biasing those locations repulsive to the charged reactant where the polymer does not include the specified monomer at said selected position, selectively reacting the specified monomer, and repeating the above steps by sequentially providing charged reactants to the device, and biasing the locations attractive and repulsive to include or exclude, respectively, a monomer at the selected positions. - View Dependent Claims (7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22)
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Specification