Nanopore sequencing of polynucleotides with multiple passes
View Patent ↗Provided are polynucleotide constructs useful in a nanopore analysis using enzyme activity. The polynucleotide constructs include a strand portion of interest to be analyzed in the nanopore analysis and having a 5′ end and a 3′ end, and a folded sequence located 3′ or 5′ of and adjacent to an end of the strand portion of interest, where the folded sequence can block the activity of a processive enzyme. In some embodiments, the polynucleotide constructs further include an enzyme binding sequence located 3′ of and adjacent to an end of the folded sequence, and an enzyme displacement sequence located 5′ of the strand portion of interest. Such polynucleotide constructs further include a threading sequence located 5′ of the enzyme displacement sequence and at a 5′ terminal end of the polynucleotide construct, where the processive enzyme has a processive activity in a direction from 3′ to 5′ on the polynucleotide construct.
1. A polynucleotide construct useful in a nanopore analysis using enzyme activity, comprising:
(a) a strand portion of interest to be analyzed in said nanopore analysis and having a 5′ end and a 3′ end;
(b) a folded sequence located 3′ of and adjacent to an end of the strand portion of interest, wherein the folded sequence can block the activity of a processive enzyme;
(c) an enzyme binding sequence located 3′ of and adjacent to an end of the folded sequence and wherein the enzyme binding sequence can bind to the processive enzyme;
(d) an enzyme displacement sequence located 5′ of the strand portion of interest; and
(e) a threading sequence located 5′ of the enzyme displacement sequence and at a 5′ terminal end of the polynucleotide construct,
wherein the processive enzyme has a processive activity in a direction from 3′ to 5′ on the polynucleotide construct.
2. The construct of claim 1 , wherein the strand portion of interest is double stranded.
3. The construct of claim 1 , wherein the enzyme binding sequence comprises a single-stranded portion.
4. The construct of claim 1 , wherein the folded sequence comprises a G quadruplex.
5. The construct of claim 4 , wherein the G quadruplex comprises one of SEQ ID NO: 1, 2, 3, or 4.
6. The construct of claim 1 , wherein the enzyme binding sequence comprises the sequence CCCCC and the polynucleotide construct is DNA.
7. The construct of claim 1 , wherein the enzyme displacement sequence comprises a plurality of abasic nucleotide sugars.
8. A polynucleotide construct useful in a nanopore analysis using enzyme activity, comprising:
(a) a strand portion of interest to be analyzed in said nanopore analysis and having a 5′ end and a 3′ end;
(b) a folded sequence located 5′ of and adjacent to an end of the strand portion of interest, wherein the folded sequence can block the activity of a processive enzyme;
(c) an enzyme binding sequence located 5′ of and adjacent to an end of the folded sequence, wherein the enzyme binding sequence can bind to the processive enzyme;
(d) an enzyme displacement sequence located 3′ of the strand portion of interest; and
(e) a single-stranded threading sequence, located 3′ of the enzyme displacement sequence and at a 3′ terminal end of the polynucleotide construct,
wherein the processive enzyme has a 5′ to 3′ processive activity.
9. The construct of claim 8 , wherein the strand portion of interest is double stranded.
10. The construct of claim 8 , wherein the enzyme binding sequence comprises a single-stranded portion.
11. The construct of claim 8 , wherein the folded sequence comprises a G quadruplex.
12. The construct of claim 11 , wherein the G quadruplex comprises one of SEQ ID NO: 1, 2, 3, or 4.
13. The construct of claim 8 , wherein the enzyme binding sequence comprises the sequence CCCCC and the polynucleotide construct is DNA.
14. The construct of claim 8 , wherein the enzyme displacement sequence comprises a plurality of abasic nucleotide sugars.