Manipulation of fluids, fluid components and reactions in microfluidic systems
Microfluidic structures and methods for manipulating fluids, fluid components, and reactions are provided. In one aspect, such structures and methods can allow production of droplets of a precise volume, which can be stored/maintained at precise regions of the device. In another aspect, microfluidic structures and methods described herein are designed for containing and positioning components in an arrangement such that the components can be manipulated and then tracked even after manipulation. For example, cells may be constrained in an arrangement in microfluidic structures described herein to facilitate tracking during their growth and/or after they multiply.
1. A method for partitioning a fluid sample, the method comprising:
providing a microfluidic device having a substrate comprising a plurality of microwells in fluid communication with an inlet;
introducing a first fluid into the inlet of the microfluidic device, the first fluid comprising a biological sample and a plurality of beads, each bead comprising a reactive component for binding a target molecule from the biological sample to the bead;
introducing a second fluid immiscible with the first fluid into the microfluidic device and flowing the second fluid towards each of the plurality of microwells so as to form partitions of fluid in corresponding microwells, each partition of fluid comprising a subvolume of the first fluid, including at least the biological sample and a single bead, wherein each partition of fluid is separated from one another by the second fluid; and
maintaining each partition of fluid in corresponding microwells for detection of contents in each partition of fluid.
2. The method of claim 1 , wherein each partition of fluid is at least partially surrounded by the second fluid.
3. The method of claim 1 , wherein the second fluid is an oil.
4. The method of claim 1 , wherein the target molecule is a single biological molecule.
5. The method of claim 1 , wherein the target molecule is a protein.
6. The method of claim 1 , further comprising monitoring one or more of the partitions of fluid and detecting, with an optical detector, emissions from one or more detectable labels associated with one or more beads.
7. The method of claim 6 , further comprising determining the presence of the target molecules based on the detection of emissions.
8. The method of claim 6 , wherein the optical detector is a fluorescence detector.
9. The method of claim 8 , further comprising measuring, with the fluorescence detector, an intensity of a fluorescent signal emitted from at least one of the detectable labels.
10. The method of claim 8 , further comprising capturing one or more images of a fluorescent signal emitted from at least one of the detectable labels.
11. The method of claim 6 , wherein, upon a reaction in at least one partition of fluid, the emissions are emitted from one or more of the detectable labels.
12. The method of claim 11 , wherein the reaction is a polymerase-chain reaction (PCR).
13. A method for partitioning a fluid sample, the method comprising:
providing a microfluidic device having a substrate comprising a plurality of regions in fluid communication with an inlet;
introducing a first fluid into the inlet of the microfluidic device, wherein the first fluid is aqueous, the first fluid comprising a biological sample and a plurality of beads, each bead comprising a reactive component for binding a target protein molecule from the biological sample to the bead;
partitioning the first fluid into a plurality of aqueous fluid partitions confined within a plurality of corresponding regions of the substrate by introducing a second fluid immiscible with the first fluid into the microfluidic device and flowing the second fluid towards the plurality of regions, wherein each aqueous fluid partition comprises a subvolume of the first fluid, including a single bead, and wherein each fluid partition is separated from one another by the second fluid; and
maintaining each aqueous fluid partition in corresponding regions for detection of contents in each fluid partition.
14. The method of claim 13 , wherein each aqueous fluid partition is at least partially surrounded by the second fluid.
15. The method of claim 13 , wherein the second fluid is an oil.
16. The method of claim 13 , further comprising monitoring one or more of the aqueous fluid partitions and detecting, with an optical detector, emissions from one or more detectable labels associated with one or more beads and determining the presence of target protein molecules based on the detection of emissions.