Application of Immobilized Enzymes for Nanopore Library Construction
The present disclosure relates, according to some embodiments, to methods for preparing a library for sequencing. For example, a method may comprise (a) in a coupled reaction, (i) contacting a population of nucleic acid fragments with a tailing enzyme to produce tailed fragments, and (ii) ligating to the tailed fragments a sequencing adapter with a ligase to produce adapter-tagged fragments; and/or separating adapter-tagged fragments from the tailing enzyme and the ligase to produce separated adapter-tagged fragments and, optionally, separated tailing enzyme and/or separated ligase. In some embodiments, a tailing enzyme and/or a ligase used in library preparation may be immobilized enzymes.
1 . An immobilized enzyme comprising:
an enzyme comprising a tailing enzyme or a ligase; and
a support comprising:
a magnetic bead having a first surface modification comprising a benzyl group that forms a covalent link between the enzyme and the magnetic bead.
2 . An immobilized enzyme according to claim 1 , wherein the magnetic bead further comprises a spacer between the bead surface and the benzyl group.
3 . An immobilized enzyme according to claim 2 , wherein the spacer comprises polyethylene glycol.
4 . An immobilized enzyme according to claim 1 , wherein no spacer is present between the bead surface and the benzyl group.
5 . An immobilized enzyme according to claim 1 , wherein the magnetic bead further comprises a second surface modification, the second surface modification comprising ethanolamine, polyethylene glycol, or ethanolamine and polyethylene glycol.
6 . An immobilized enzyme according to claim 1 , wherein the magnetic bead further comprises a second surface modification, the second surface modification comprising polyethylene glycol 750.
7 . An immobilized enzyme according to claim 1 , wherein the magnetic bead is free of additional surface modifications.
8 . An immobilized enzyme according to claim 1 , wherein the enzyme is an enzyme fusion.
9 . An immobilized enzyme according to claim 8 , wherein the enzyme fusion comprises:
(a) an O 6 -alkylguanine-DNA alkyltransferase, and
(b) the tailing enzyme or the ligase.
10 . An immobilized enzyme according to claim 8 , wherein the enzyme fusion comprises:
(a) a self-labeling tag reactive with a benzylguanine or a benzylcytosine, and
(b) the tailing enzyme or the ligase.
11 . An immobilized enzyme according to claim 1 , wherein the enzyme is a tailing enzyme selected from a poly(A) polymerase, a poly(G) polymerase, and a poly(U) polymerase.
12 . An immobilized enzyme according to claim 1 , wherein the enzyme is a poly(A) polymerase.
13 . An immobilized enzyme according to claim 1 , wherein the enzyme is a ligase selected from an ATP-dependent double-strand polynucleotide ligase, an NAD+-dependent double-strand DNA ligase, an NAD+-dependent double-strand RNA ligase, and a single-strand polynucleotide ligase.
14 . An immobilized enzyme according to claim 1 , wherein the enzyme is a ligase selected from an E. coli DNA ligase, a Taq DNA ligase, or a phage ligase.
15 . An immobilized enzyme according to claim 1 , wherein the enzyme is a ligase selected from a T3 DNA ligase, a T4 DNA ligase, a T7 DNA ligase, or a 9°N DNA ligase.
16 . An immobilized enzyme according to claim 1 , wherein the enzyme is a T4 DNA ligase.
17 . A composition comprising an immobilized enzyme according to claim 1 .
18 . A composition comprising an immobilized enzyme according to claim 1 , wherein the enzyme is a poly(A) polymerase or a T4 DNA ligase.
19 . A composition comprising an immobilized enzyme according to claim 1 , wherein no spacer is present between the bead surface and the benzyl group.
20 . A composition comprising an immobilized enzyme according to claim 1 , wherein the magnetic bead is free of additional surface modifications.
21 . A composition comprising:
a first immobilized enzyme according to claim 1 , wherein the enzyme is a poly(A) polymerase, and
a second immobilized enzyme according to claim 1 , wherein the enzyme is a ligase.
22 . A kit comprising an immobilized enzyme according to claim 1 and one or more of a buffer, a primer, dATP, dTTP, dGTP, dCTP, rATP, rUTP, rGTP, rCTP, and a modified nucleotide.
23 . A kit comprising an immobilized enzyme according to claim 1 and a buffer, wherein the enzyme is a poly(A) polymerase or a T4 DNA ligase.
24 . A method of preparing a library for sequencing, comprising:
(a) in a coupled reaction, (i) contacting a population of nucleic acid fragments with an immobilized poly(A) polymerase to produce tailed fragments, and (ii) ligating to the tailed fragments a sequencing adapter with a ligase to produce adapter-tagged fragments; and
(b) separating adapter-tagged fragments from the poly(A) polymerase and the ligase to produce separated adapter-tagged fragments and, optionally, separated poly(A) polymerase and/or separated ligase.
25 . A method according to claim 24 , wherein poly(A) polymerasethe ligase is an immobilized ligase.
26 . A method according to claim 24 , wherein the poly(A) polymerasepoly(A) polymerase is immobilized on a magnetic bead.
27 . A method according to claim 26 , wherein the separating the adapter tagged fragments further comprises subjecting the coupled reaction to a magnetic field.
28 . A method according to claim 24 , wherein the ligase is immobilized on a magnetic bead.
29 . A method according to claim 28 , wherein the separating the adapter tagged fragments further comprises subjecting the coupled reaction to a magnetic field.
30 . A method according to claim 24 , wherein the poly(A) polymerasepoly(A) polymerase and the ligase are immobilized on separate supports.
31 . A method according to claim 24 , wherein the poly(A) polymerasepoly(A) polymerase and the coupled reaction steps occur in a single tube, well, capillary, flow cell or surface.
32 . A method according to claim 24 , wherein the ligase is a soluble ligase.
33 . A method according to claim 24 , wherein the population of nucleic acid fragments comprise ribonucleic acid fragments.
34 . A method according to claim 24 , wherein the population of nucleic acid fragments comprise deoxyribonucleic acid fragments.
35 . A method according to claim 24 , wherein the population of nucleic acid fragments has less than 100 ng of nucleic acids.
36 . A method according to claim 24 , wherein the population of nucleic acid fragments has less than 10 ng of nucleic acids.
37 . A method according to claim 24 , further comprising:
(c) in a second coupled reaction, (i) contacting a second population of nucleic acid fragments with the separated poly(A) polymerase to produce additional tailed fragments, and (ii) ligating to the additional tailed fragments a second sequencing adapter with the separated ligase to produce additional adapter-tagged fragments, and
(d) separating the additional adapter-tagged fragments from the separated poly(A) polymerase and the separated ligase to produce separated additional adapter-tagged fragments, separated poly(A) polymerase, and separated ligase.
38 . A method according to claim 37 , further comprising:
(e) translocating the separated adapter-tagged fragments through one or more transmembrane pores;
(f) detecting electrical changes as the one or more separated adapter-tagged fragments are translocated through the one or more transmembrane pores in an insulating membrane to produce an electrical signal; and
(g) analyzing the electrical signal to generate a sequence read.
39 . A method according to claim 38 , wherein the one or more transmembrane pores retain about 90% of their initial activity after two hours.
40 . A method according to claim 38 , wherein the one or more transmembrane pores retain about 50% of their initial activity after 8 hours.
41 . A method according to claim 38 , wherein the one or more transmembrane pores produce at least 900 sequence reads per transmembrane pore.
42 . A method according to claim 24 , wherein the sequencing adapter is a single stranded adapter comprising:
a leader sequence; and
a first sequence and a second sequence, wherein the first and second sequences are complementary to each other and define a hairpin,
wherein the leader sequence is configured to thread into the one or more transmembrane pores.