Two-dimensional microfluidics for protein separations and gene analysis
View Patent ↗The invention provides a microfluidic apparatus for performing 2-D biomolecular separations. The microfluidic 2-D device may include first and second planar substrates which include at least a first dimension microchannel extending in a first direction and an array of second dimension microchannels extending in a second direction, preferably, orthogonal to the first dimension. The ends of at least some of the microchannels are in fluid communication with a plurality of reservoirs. The substrates may further include a number of microchannels and reservoirs. The reservoirs are in electrical communication with a plurality of electrodes and voltage power sources. The device enables two dimensional separations of proteins, DNA and other biomolecules. According to another aspect of the invention, an array of tertiary microchannels extending in a third direction may be utilized.
1. A microfluidic apparatus for performing two-dimensional bimolecular separations, the apparatus comprising:
at least one first dimension microchannel having at least a first surface and a second surface;
an array of second dimension microchannels intersecting the first surface of the at least one first dimension microchannel;
an array of tertiary microchannels intersecting the second surface of the at least one first dimension microchannel;
means for performing a first continuous separation in the at least one first dimension microchannel to produce a separated sample, wherein the first continuous separation includes isoelectric focusing;
means for transferring the separated sample directly from the at least one first dimension microchannel to the second dimension microchannels; and
means for introducing a first media in the at least one first dimension microchannel and a second media into the array of second dimension microchannels.
2. The apparatus of claim 1 wherein the means for introducing comprises pressure filling means.
3. The apparatus of claim 1 wherein the means for introducing is operable, prior to introducing a first media in the at least one first dimension microchannel, to fill the at least one first dimension microchannel and second dimension microchannels with a second media, electroosmotically remove the second media from one of the first dimension microchannel, and introducing a first media into the at least one first dimension microchannel.
4. The apparatus of claim 1 further comprising a hydrodynamic barrier between the at least one first dimension microchannel and second dimension microchannels to enable each to be filled with a different media.
5. The apparatus of claim 1 , wherein the biomolecular separation is to be performed on a biomolecular material and the biomolecular material comprises protein.
6. The apparatus of claim 1 wherein the means for transferring the separated sample further comprises means for substantially retaining the first dimension separation upon transfer to the second dimension.
7. The apparatus of claim 1 , wherein the first media comprises a media for isoelectric focusing in the first dimension, comprising carrier ampholytes for the creation of pH gradient in the first microchannel.
8. The apparatus of claim 1 , wherein the second media comprises a media for size based separation of SDS-protein complexes in the second dimension based on their differences in electrophoretic mobility inside a polymer sieving matrix.
9. The apparatus of claim 1 , wherein the first media is a sieving matrix selected from the group consisting of:
cross-linked polyacrylamide, linear polyacrylamide, polydimethylamide, N-acrylamoniethoxyethanol, hydroxyethylcellulose [HEC], poly(ethylene glycol), poly(ethylene oxide) [PEO], poly(vinylpyrrolidone) [PVP], nonionic polymeric surfactants, or n-alkyl polyoxyethylene ethers.
10. The apparatus of claim 1 , further comprising a detector placed near an end of the array of second-dimension separation microchannels for differential display of protein expressions.
11. The apparatus of claim 1 , further comprising a detector capable of monitoring substantially all of the full length and breadth of the array of second-dimension separation microchannels for differential display of protein expressions.
12. The apparatus of claim 1 , further comprising a detector to monitor the performance of isoelectric focusing in the at least one first dimension microchannel, wherein proteins may be covalently labeled with a suitable florescent dye and detected by a suitable florescence detector.
13. The apparatus of claim 1 , further comprising a detector to monitor the performance of isoelectric focusing in first dimension microchannels, wherein proteins in a biomolecular sample may be covalently labeled with a suitable florescent dye and detected by a suitable florescence detector and the microchannels are formed from a substrate optically transparent at the wavelengths used for the fluorescence detection.
14. The apparatus of claim 1 further comprising an integrated optical detection system.
15. The apparatus of claim 1 further comprising an integrated laser-induced fluorescence detection system.
16. A microfluidic apparatus for performing two dimensional bio-molecular separations, the apparatus comprising:
at least one first dimension microchannel having at least a first surface and a second surface;
an array of second dimension microchannels intersecting the first surface of the at least one first dimension microchannel;
an array of tertiary microchannels intersecting the second surface of the at least one first dimension microchannel;
means for performing a first biomolecular separation in the at least one first dimension microchannel to produce a separated sample, wherein the first biomolecular separation includes size-based separation;
means for transferring the separated sample to the microchannels of the array of second dimension microchannels; and
means for performing a second separation in the second dimension microchannels, where the second separation is performed by applying a temperature gradient.
17. The apparatus of claim 16 wherein the biomolecular separation is performed on a biomolecular material and the biomolecular material comprises DNA.
18. A microfluidic apparatus for performing two-dimensional protein separations, the apparatus comprising:
at least one first dimension microchannel for performing a first protein separation, wherein the first protein separation includes isoelectric focusing;
an array of one or more second dimension microchannel for performing a second protein separation, wherein the second protein separation includes size-based separation;
an array of one or more tertiary microchannels;
one or more electrodes that intersect one of the one or more second dimension microchannels or the one or more tertiary microchannels; and
one or more voltage sources operatively connected to the one or more electrodes to control the voltage at the points of intersection of the microchannels.