EFFICIENT OPTICAL ANALYSIS OF POLYMERS USING ARRAYS OF NANOSTRUCTURES

• US 20160115531A1
• Filed: 10/23/2015
• Published: 04/28/2016
• Est. Priority Date: 10/24/2014
• Status: Active Grant

• Current Assignee: Quantapore, Inc.
• Original Assignee: Quantapore, Inc.
• Inventors: Huber, Martin, Davidson, Stuart
• Granted Patent: US 9,624,537 B2
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C12Q 2535/122 Massive parallel sequencing
• CPC Class Codes: C12Q 2563/107 fluorescence
• CPC Class Codes: C12Q 2565/125 Electrophoretic separation
• CPC Class Codes: C12Q 2565/631 being a biochannel or pore
• CPC Class Codes: G01N 2021/6439 with indicators, stains, dyes, tags, labels, marks
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates
• CPC Class Codes: G01N 21/648 using evanescent coupling or surface plasmon coupling for the excitation of fluorescence
• CPC Class Codes: G01N 21/76 Chemiluminescence; Bioluminescence
• CPC Class Codes: G01N 2201/06113 Coherent sources; lasers
• CPC Class Codes: G01N 33/48721 Investigating individual macromolecules, e.g. by translocation through nanopores Coulter counters in general G01N15/12; fabrication methods for nanoscale apertures B81B1/00; sequencing of nucleic acids C12Q1/68

Abstract

The invention is directed to methods and apparatus for detecting sequences of optical signals from parallel reactions on an array of nanostructures, such as nanopores, nanowells, or nanoparticles. In accordance with the invention, an array of nanostructures is provided, each nanostructure comprising a reaction site and each capable of confining a reaction that generates a sequence of optical signals, and the nanostructures of the array being arranged in clusters each comprising a number of nanostructures. Each different cluster is disposed within a different resolution limited area and the number of nanostructures in each cluster is either greater than one or a random variable with an average value greater than zero. Optical signals from reactions in the nanostructures are detected by an optical system operatively associated with the array.

Claims

1. A device for analyzing polymers each having optical labels attached to a sequence of monomers, the device comprising:

a nanopore array separating a first chamber and a second chamber, wherein nanopores of the nanopore array each connect the first chamber and the second chamber and are arranged in clusters such that each different cluster of nanopores is disposed within a different resolution limited area;

a polymer translocating system for moving polymers in the first chamber to the second chamber through the nanopores of the nanopore array; and

a detection system for collecting optical signals generated by optical labels attached to polymers whenever an optical label exits a nanopore within a resolution limited area.

2. The device of claim 1 wherein said clusters are arranged in a rectilinear array or in a hexagonal array.

3. The device of claim 1 wherein each of said clusters comprises a plurality of nanopores or each of said clusters comprises a number of nanopores which is a random variable with an average value greater than zero.

4. The device of claim 1 wherein said polymers are polynucleotides and wherein said detection system determines numbers of functional nanopores within each of said resolution limited areas from said collected optical signals and varies an electrical field across said nanopore array to maximize a rate of sequence determination by said nanopore array.

5. A method of analyzing polymers each having a sequence of optical labels comprising:

providing a nanopore array wherein each nanopore has a bore capable of providing fluid communication between a first chamber and a second chamber, and the nanopore array having at least one resolution limited area containing a plurality of nanopores;

translocating polymers through nanopores of the nanopore array;

collecting and integrating optical signals from polymers translocating through nanopores in each of the resolution limited areas during a predetermined interval to obtain an integrated signal for each of the resolution limited areas; and

determining a number of functional nanopores within each of the resolution limited areas by a relative level of its integrated signal.

6. The method of claim 5 further including the step of selecting a polymer concentration and/or polymer flux to maximize sequencing throughput of the nanopore array.

7. The method of claim 6 wherein said polymers are polynucleotides and said step of selecting comprises adjusting said polymer flux to maximize sequencing throughput by varying an electrical field strength across said nanopore array.

8. A device for analyzing polymers each having a sequence of optical labels comprising:

a solid phase membrane separating a first chamber and a second chamber, the solid phase membrane having an array of apertures each connecting the first chamber and the second chamber, the apertures of the array being arranged in clusters each having a plurality of apertures and each different cluster being disposed within a different resolution limited area;

protein nanopores immobilized in the apertures, the immobilized protein nanopores having an active fraction wherein each immobilized protein of the active fraction is capable of translocating a polymer from the first chamber to the second chamber through a bore; and

a detection system for collecting optical signals generated by optical labels whenever an optical label exits a bore of a protein nanopore within a resolution limited area.

9. The device of claim 8 wherein said polymers comprise polynucleotides and wherein said detection system determines numbers of functional nanopores within each of said resolution limited areas from said collected optical signals and varies an electrical field across said nanopore array to maximize a rate of determining said sequences of optical labels by said nanopore array.

10. A method of sequencing polynucleotides each having a sequence of optical labels comprising:

(a) translocating single stranded polynucleotides at a concentration and flux through a nanopore array, wherein substantially every nucleotide of each single stranded polynucleotides is labeled with an optical label capable of generating an optical signal indicative of the nucleotide to which it is attached, and wherein the nanopore array comprises clusters of nanopores, each cluster comprising a number of nanopores, wherein each different cluster is disposed within a different resolution limited area and wherein the number of nanopores in each cluster is either greater than one or is a random variable with an average value greater than zero;

(b) exposing the optical labels of each nucleotide to excitation radiation upon exiting a nanopore;

(c) measuring in each resolution limited region on the nanopore array optical signals generated by optical labels exiting nanopores to identify the nucleotide to which the optical label is attached whenever such optical signals are from a single optical label; and

(d) determining a nucleotide sequence of the polynucleotide from a sequence of optical signals from single optical labels.

11. The method of claim 10 wherein concentration of said polynucleotides and/or flux of said polynucleotides through said nanopore array are adjusted to maximize sequence-able nanopores in the array.

12. The method of claim 10 wherein said flux of said single stranded polynucleotides is controlled to maximize the number of sequence-able nanopores in the array by controlling an electrical potential across said nanopore array.

13. An apparatus for detecting sequences of optical signals from parallel reactions on an array, the apparatus comprising:

an array of nanostructures each comprising a reaction site and each capable of confining a reaction that generates a sequence of optical signals, the nanostructures of the array being arranged in clusters each comprising a number of nanostructures and each different cluster of nanostructures being disposed within a different resolution limited area; and

an optical system operatively associated with the array for detecting optical signals from the reactions.

14. The apparatus of claim 13 wherein said nanostructure is selected from the group consisting of nanopores, nanowells and nanoparticles.

15. The apparatus of claim 14 wherein said number of nanostructures in each of said clusters is either greater than one or a random variable with an average value greater than zero.

16. The apparatus of claim 15 wherein said nanostructures are nanopores and wherein said array comprises a solid phase membrane separating a first chamber and a second chamber, the solid phase membrane having a plurality of apertures each connecting the first chamber and the second chamber and each being disposed in a cluster;

and protein nanopores immobilized in the apertures, the immobilized protein nanopores having an active fraction wherein each immobilized protein of the active fraction is capable of translocating a polymer from the first chamber to the second chamber through a bore.

17. The apparatus of claim 16 wherein said reactions at said protein nanopores are FRET interactions between donors and acceptors of a FRET pair, each acceptor being attached to a monomer of said polymer and each acceptor being capable of generating an optical signal indicative of the monomer to which it is attached.

18. The apparatus of claim 15 wherein said nanostructures are nanopores and wherein said array comprises a solid phase membrane separating a first chamber and a second chamber, the solid phase membrane having a plurality of apertures each connecting the first chamber and the second chamber and each being spanned by a lipid bilayer;

the lipid bilayers having disposed therein protein nanopores to form said clusters, such that said number of protein nanopores in each cluster is said random variable with said average value greater than zero.

19. The apparatus of claim 18 wherein said reactions at said protein nanopores are FRET interactions between donors and acceptors of a FRET pair, each donor being attached to a protein nanopore and each acceptor being attached to a monomer of said polymer, wherein each acceptor being capable of generating an optical signal indicative of the monomer to which it is attached.

20. The apparatus of claim 15 wherein said nanostructures are nanowells each comprising a zero mode waveguide.