Systems and methods for automated reusable parallel biological reactions
A method comprises magnetically holding a bead carrying biological material (e.g., nucleic acid, which may be in the form of DNA fragments or amplified DNA) in a specific location of a substrate, and applying an electric field local to the bead to isolate the biological material or products or byproducts of reactions of the biological material. For example, the bead is isolated from other beads having associated biological material. The electric field in various embodiments concentrates reagents for an amplification or sequencing reaction, and/or concentrates and isolates detectable reaction by-products. For example, by isolating nucleic acids around individual beads, the electric field can allow for clonal amplification, as an alternative to emulsion PCR. In other embodiments, the electric field isolates a nanosensor proximate to the bead, to facilitate detection of at least one of local pH change, local conductivity change, local charge concentration change and local heat. The beads may be trapped in the form of an array of localized magnetic field regions.
1. A method for sequencing, comprising:
(a) providing a plurality of particles, wherein each particle of said plurality is coupled to on average at most one nucleic acid molecule;
(b) performing simultaneous nucleic acid amplification reactions on said nucleic acid molecules coupled to said particles, wherein said nucleic acid amplification reactions are performed while subjecting the particles to an electric field, thereby producing isolated, clonally-amplified nucleic acid molecules coupled to said plurality of particles;
(c) performing nucleic acid extension reactions on said clonally-amplified nucleic acid molecules using primers that hybridize to said clonally-amplified nucleic acid molecules; and
(d) detecting nucleic acid incorporation events from said extension reactions using a sensor array to determine a sequence of each of said clonally-amplified nucleic acid molecules, wherein each particle of said plurality of particles is adjacent to a sensor of said sensor array, and wherein each said sensor of said sensor array comprises two electrodes that are within a Debye length of their respective individual particle or within a Debye length of a nucleic acid molecule on said individual particle.
2. The method of claim 1 , wherein said nucleic acid amplification reactions are emulsion free.
3. The method of claim 1 , further comprising, subsequent to (b), separating particles carrying clonally-amplified nucleic acid molecules from particles not carrying clonally-amplified nucleic acid molecules.
4. The method of claim 1 , wherein (b) is performed with the plurality of particles held adjacent to the sensor array.
5. The method of claim 1 , wherein, in (c), the particles are at least one of electrically and magnetically immobilized.
6. The method of claim 1 , further comprising releasing one or more of said plurality of particles.
7. The method of claim 1 , wherein, in (d), detecting said nucleic acid incorporation events further comprises using an individual sensor among the plurality of sensors to detect at least one of local impedance change and local conductivity change.
8. The method of claim 1 , wherein the electric field isolates or concentrates one or more of template DNA fragments, primers, polymerase, and dNTPs around each of the particles.
9. The method of claim 1 , wherein the electric field isolates or concentrates products of nucleic acid amplification reactions.
10. A method for nucleic acid sequencing, comprising:
(a) directing a plurality of particles onto an array of sensors, wherein an individual particle comprises a nucleic acid molecule, and wherein an individual sensor of said array comprises a pair of electrodes that are electrically coupled to a Debye length of said individual particle during nucleic acid sequencing;
(b) positioning said individual particle at said individual sensor;
(c) directing a plurality of primers onto said array;
(d) performing a primer extension reaction at said individual sensor; and
(e) during or subsequent to performing said primer extension reaction, measuring a change in impedance of said individual particle with the aid of said pair of electrodes that are each electrically coupled to said Debye length of said individual particle.
11. The method of claim 10 , further comprising amplifying said nucleic acid molecule prior to (d).
12. The method of claim 11 , wherein said nucleic acid molecule is amplified while subjecting said individual particle to an electric field.
13. The method of claim 11 , wherein said nucleic acid molecule is amplified while said individual particle is held at said given sensor.
14. The method of claim 1 , wherein an individual electrode of said two electrodes has a Debye length.
15. The method of claim 14 , wherein said Debye length of said individual electrode is within said Debye length of said individual particle or said Debye length of said nucleic acid molecule on said individual particle.
16. The method of claim 10 , wherein, in (e), the electrodes of said pair of electrodes are within said Debye length of said individual particle.
17. The method of claim 16 , wherein an individual electrode of said pair of electrodes has a Debye length.
18. The method of claim 17 , wherein said Debye length of said individual electrode is within said Debye length of said individual particle.