Multiplexed microcolumn devices and processes for selection of nucleic acid aptamers

Patent metadata

Field	Value
Publication number	US-10132798-B2
Application number	US-201314400229-A
Country	US
Kind code	B2
Filing date	May 13, 2013
Priority date	May 11, 2012
Publication date	Nov 20, 2018
Grant date	Nov 20, 2018

Abstract

The present invention relates to a microcolumn device for selecting nucleic acid aptamers for single and multiple target molecules, as well as a method for making the microcolumn device. The present invention also relates to a system for selecting nucleic acid aptamers for single and multiple target molecules. The present invention further relates to methods of using the microcolumn device for selecting nucleic acid aptamers for multiple target molecules. Kits that include one or more microcolumn device and/or system of the present invention are also disclosed.

First claim

What is claimed is:

1. A microcolumn device for selecting nucleic acid aptamers for single and multiple target molecules, said microcolumn device comprising:
a body comprising an inlet end and a directly opposing outlet end, a recessed portion extending into the body from the outlet end and forming a compartment for housing a frit, and a microfluidic channel disposed between the inlet end and the recessed portion, wherein the microfluidic channel has a volume capacity of between about 0.5 μL and about 250 μL;
a frit disposed in the recessed portion; and
a pair of adapters comprising an inlet adapter bonded to the inlet end of the body and a directly opposing outlet adapter bonded to the outlet end of the body, wherein each adapter includes a hollow passageway for passing a liquid sample there through, and wherein each adapter includes a connector region for effectuating serial fluid communication of a plurality of microcolumn devices.

2. The microcolumn device according to claim 1 , wherein the body comprises a biocompatible plastic polymer selected from the group consisting of poly(ethylene terephthalate glycol) (PETg), polyvinyl chloride (PVC), and poly(methyl methacrylate) (PMMA).

3. The microcolumn device according to claim 1 further comprising:
an affinity chromatography resin disposed in the microfluidic channel of the body.

4. The microcolumn device according to claim 3 , wherein the affinity chromatography resin comprises an immobilized target molecule.

5. The microcolumn device according to claim 4 , wherein the immobilized target is labeled.

6. The microcolumn device according to claim 4 , wherein the immobilized target molecule is a protein or polypeptide, a carbohydrate, a lipid, a small molecule, a pharmaceutical agent, an organic non-pharmaceutical agent, a macromolecular complex, a virus particle, or a cell.

7. The microcolumn device according to claim 4 , wherein the immobilized target molecule is provided from a mixture of lysed cells, or a mixture of purified, partially purified, or non-purified protein.

8. A system for selecting nucleic acid aptamers for single and multiple target molecules, said system comprising:
a plurality of microcolumn devices in serial fluid communication with one another, wherein each microcolumn device comprises:
a body comprising an inlet end and a directly opposing outlet end, a recessed portion extending into the body from the outlet end and forming a compartment for housing a frit, and a microfluidic channel disposed between the inlet end and the recessed portion, wherein the microfluidic channel has a volume capacity of between about 0.5 μL and about 250 μL;
a frit disposed in the recessed portion; and
a pair of adapters comprising an inlet adapter bonded to the inlet end of the body and a directly opposing outlet adapter bonded to the outlet end of the body, wherein each adapter includes a hollow passageway for passing a liquid sample there through, and wherein each adapter includes a connector region for effectuating serial fluid communication of the plurality of microcolumn devices.

9. The system according to claim 8 further comprising:
an affinity chromatography resin disposed in the microfluidic channel of the body of each microcolumn device.

10. The system according to claim 9 , wherein the affinity chromatography resins contained in each microcolumn device are the same or different.

11. The system according to claim 9 , wherein the affinity chromatography resin comprises an immobilized target molecule, said immobilized target molecule being labeled or unlabeled.

12. The system according to claim 11 , wherein the immobilized target molecules contained in each microcolumn device are the same or different.

13. The system according to claim 8 , wherein union connectors are used to effectuate the serial fluid communication of the plurality of microfluidic devices.

14. A method of making a microcolumn device for selecting nucleic acid aptamers for single and multiple target molecules, said method comprising:
providing a body comprising an inlet end and a directly opposing outlet end, a recessed portion extending into the body from the outlet end and forming a compartment for housing a frit, and a microfluidic channel disposed between the inlet end and the recessed portion, wherein the microfluidic channel has a volume capacity of between about 0.5 μL and about 250 μL;
disposing a fit in the recessed portion of the body; and
attaching a pair of adapters to the body, wherein an inlet adapter is bonded to the inlet end of the body and a directly opposing outlet adapter is bonded to the outlet end of the body, wherein each adapter includes a hollow passageway for passing a liquid sample there through, and wherein each adapter includes a connector region for effectuating serial fluid communication of multiple microcolumn devices.

15. The method according to claim 14 , wherein the body comprises a biocompatible plastic polymer selected from the group consisting of poly(ethylene terephthalate glycol) (PETg), polyvinyl chloride (PVC), and poly(methyl methacrylate) (PMMA).

16. The method according to claim 14 further comprising:
disposing an affinity chromatography resin in the microfluidic channel of the body.

17. The method according to claim 16 , wherein the affinity chromatography resin comprises an immobilized target molecule.

18. The method according to claim 17 , wherein the immobilized target is labeled.

19. The method according to claim 17 , wherein the immobilized target molecule is a protein or polypeptide, a carbohydrate, a lipid, a small molecule, a pharmaceutical agent, an organic non-pharmaceutical agent, a macromolecular complex, a virus particle, or a cell.

20. The method according to claim 17 , wherein the immobilized target molecule is provided from a mixture of lysed cells, or a mixture of purified, partially purified, or non-purified protein.

21. A kit comprising one or more microcolumn devices according to claim 1 .

22. The kit according to claim 21 further comprising one or more of the following:
one or more affinity chromatography resins, one or more labels for tagging a target molecule of interest, a random pool of nucleic acid molecules, wash buffer, binding buffer, blocking buffer, reagents for carrying out reverse transcription, polymerase chain reaction, and/or transcription, and directions for carrying out selection of aptamers to multiple target molecules using a plurality of the microcolumn devices connected in series and subsequently arranged in a standalone or parallel configuration.

23. A kit comprising a system according to claim 8 .

24. The kit according to claim 23 further comprising one or more of the following:
one or more affinity chromatography resins, one or more labels for tagging a target molecule of interest, a random pool of nucleic acid molecules, wash buffer, binding buffer, blocking buffer, reagents for carrying out reverse transcription, polymerase chain reaction, and/or transcription, and directions for carrying out selection of aptamers to multiple target molecules using a plurality of the microcolumn devices connected in series and subsequently arranged in a standalone or parallel configuration.

25. The microcolumn device according to claim 1 , wherein said frit is effective to maintain an affinity chromatography resin in the microfluidic channel while at the same time allow a liquid sample to pass through

Assignees

• Univ Cornell

Inventors

• Craighead Harold G
• Latulippe David R
• Lis John T
• Ozer Abdullah
• Szeto Kylan

Classifications

• G01N33/5302 Primary

  Apparatus specially adapted for immunological test procedures · CPC title

• C12N15/115

  Aptamers, i.e. nucleic acids binding a target molecule specifically and with high affinity without hybridising therewith {; Nucleic acids binding to non-nucleic acids, e.g. aptamers} · CPC title

• C12N2330/00

  Production · CPC title

• C12N2310/16

  Aptamers · CPC title

• G01N33/5308 Primary

  for analytes not provided for elsewhere, e.g. nucleic acids, uric acid, worms, mites · CPC title