Nanopore sequencing of polynucleotides with multiple passes

1. A method for analyzing properties of a target portion of a polynucleotide using a nanopore in a membrane separating a cis fluid area from a trans fluid area, and a voltage source and current detector, comprising:

(a) adding to the cis fluid side a polynucleotide comprising a target portion to be analyzed, said polynucleotide comprising in order: an enzyme binding site, an enzyme blocking sequence, the target portion, an enzyme displacement region and a threading sequence;

(b) adding a processive enzyme to the fluid on the cis side and allowing the processive enzyme to bind to the enzyme binding site of the polynucleotide on the cis side;

(c) drawing the polynucleotide, beginning with the threading sequence, through the nanopore to the trans side by a charge on the polynucleotide and thereby removing blocking by the enzyme blocking sequence on the cis side;

(d) allowing the processive enzyme, bound to the enzyme binding site, to processively draw the polynucleotide from step (c) through the nanopore, from the trans side towards the cis side, while detecting current changes from nucleotides passing through the nanopore, said current changes being indicative of polynucleotide properties;

(e) said processive enzyme being displaced by the displacement region when it reaches the displacement region by the processive drawing of step (d); and

(f) whereby displacement of the processive enzyme in step (e) causes voltage to again draw the polynucleotide through the nanopore, as in step (c), and a processive enzyme that has attached again to the polynucleotide on the cis side, processively draws the polynucleotide through the nanopore.

2. The method of claim 1 , wherein said detecting current changes occurs more than once on a single polynucleotide in a single or multiple nanopores.

3. The method of claim 1 , wherein said nanopore is one of carbon, alpha-hemolysin, and MspA.

4. The method of claim 1 , wherein the processive enzyme is a helicase and the enzyme binding site is specific for said helicase.

5. The method of claim 4 , wherein the helicase is an He1308 helicase having at least 95% sequence identity to HELQ.

6. The method of claim 1 , wherein the enzyme blocking sequence is a polynucleotide region containing at least one hairpin turn.

7. The method of claim 6 , wherein the enzyme blocking sequence is a G-quadruplex.

8. The method of claim 1 , wherein enzyme displacement region is a number of adjacent abasic nucleotide residues.

9. The method of claim 1 , wherein the analyzing comprises detecting non-canonical bases.

10. The method of claim 1 , wherein the polynucleotide is RNA.

11. A method for nanopore-based analysis of a polynucleotide, comprising by modifying the polynucleotide to comprise, at one end region, an enzyme binding site adjacent to an enzyme activity blocking structure and, at a second end region, an enzyme displacement region, wherein the method further comprises the use of an enzyme that translocates the polynucleotide through a nanopore against a voltage force when the enzyme activity blocking structure is removed, and said enzyme blocking structure is reconstituted by movement of the enzyme.

12. A method comprising:

providing a polynucleotide comprising in order: an abasic region, a region to be analyzed, a GQ fold, and an enzyme binding site; and

removing one enzyme molecule at the abasic region and allowing another enzyme molecule to bind at the enzyme binding site.