Coupling method
The invention relates to a new method of determining the presence, absence or characteristics of an analyte. The analyte is coupled to a membrane. The invention also relates to nucleic acid sequencing.
1. A method for enhancing a target polynucleotide concentration on a surface during nanopore sequencing, the method comprising:
(i) contacting a target polynucleotide construct to a surface comprising a nanopore, and a solid-state membrane supporting a lipid bilayer, wherein the target polynucleotide construct comprises:
(a) a single stranded DNA (ssDNA) leader;
(b) a target polynucleotide; and
(c) one or more reactive groups that interact with the lipid bilayer, under conditions under which the one or more reactive groups interacts with the lipid bilayer and tethers the target polynucleotide construct to the lipid bilayer resulting in enhanced concentration of the target polynucleotide on the surface in proximity to the nanopore; and
(ii) detecting the target polynucleotide using the nanopore.
2. The method according to claim 1 , wherein the target polynucleotide is a DNA polynucleotide or an RNA polynucleotide.
3. The method according to claim 1 , wherein the nanopore is a protein nanopore.
4. The method according to claim 1 , wherein each of the one or more reactive groups comprises a lipid, cholesterol, or fatty acyl chain.
5. The method according to claim 1 , wherein the target polynucleotide construct is tethered to the lipid bilayer at 2, 3, or 4 points.
6. The method according to claim 1 , wherein the ssDNA leader is negatively charged.
7. The method according to claim 6 , wherein the ssDNA leader is positioned 5′ relative to the target polynucleotide.
8. The method according to claim 1 , wherein the target polynucleotide construct is transiently tethered to the lipid bilayer.
9. The method according to claim 1 , wherein the detecting comprises applying an electrical current to the surface such that the tethered target polynucleotide construct moves across the lipid bilayer, thereby increasing interaction of the tethered target polynucleotide construct with the nanopore.
10. The method according to claim 9 , wherein upon application of the electrical current, the ssDNA leader of the tethered target polynucleotide construct is captured by the nanopore.
11. The method according to claim 1 , wherein the detecting comprises measuring current flowing through the nanopore as the target polynucleotide translocates through the nanopore.