Method and system for linearization and translocation of single protein molecules through nanopores
A method and system for performing single molecule proteomics utilizing a nanopore sensor to measure an electronic signature of protein or peptide being transported through the nanopore from a first chamber to a second chamber. The protein's electronic signature is a function of ionic current over time. The method and system utilizing an agent, such as guanidinium chloride, to bind to the nanopore's interior and provide an electroosmotic force within the nanopore. The electroosmotic force, in some embodiments, enables stretching and unfolding of the protein during transport through the nanopore. The agent may also or alternatively induce the unfolding of the protein before transport through the nanopore and/or provide force moving the protein through the nanopore.
1. A method of performing single molecule proteomics, the method comprising:
containing a fluid in a structure, the structure defining an interior cavity and a barrier dividing the interior cavity into a first chamber and a second chamber, the barrier containing a channel structure defining a nanopore therethrough fluidically coupling the first and second chambers, the nanopore having a flow path bounded by an interior surface of the channel structure; wherein the fluid includes (i) a protein comprising amino acid residues and, (ii) an agent, the agent capable of enabling stretching and unfolding of the protein;
binding particles of the agent to the interior surface of the channel structure defining the nanopore to establish bound particles, the bound particles causing the amino acid residues of the protein passing through the flow path of the nanopore to orient themselves as a linear series of amino acid residues;
applying a voltage gradient between the first chamber and the second chamber via the flow path, the voltage gradient inducing an ionic flow through the flow path of the nanopore;
observing an electronic signature produced by interactions between ions comprising the ionic flow and the linear series of amino acid residues of the protein passing through the flow path of the nanopore altering the ionic current through the flow path of the nanopore; and
determining a property of the protein based on the observed electronic signature.
2. The method of claim 1 wherein the agent includes guanidinium ions.
3. The method of claim 1 wherein binding the particles of the agent includes the bound particles causing the amino acid residues of the protein passing through the flow path of the nanopore to orient themselves as a linear series of amino acid residues by generating an electroosmotic force in the flow path of the nanopore.
4. The method of claim 3 wherein the electroosmotic force varies linearly with respect to a magnitude of the voltage gradient.
5. The method of claim 1 further comprising connecting the protein to a charged tail configured to guide the protein into the flow path when the voltage gradient is applied.
6. The method of claim 1 further comprising containing in the first chamber an enzyme that is capable of causing the protein to unfold.
7. The method of claim 6 wherein the agent is not present in the first chamber.
8. The method of claim 1 wherein the voltage gradient is a first voltage gradient, and wherein the method further comprises:
connecting a DNA tail to the protein;
applying a second voltage gradient across the first and the second chambers via the flow path, the second voltage gradient of sufficient strength to cause a section of the DNA tail to pass through the nanopore prior to applying the first voltage gradient; and
activating an enzyme, contained in the first chamber, to draw, in discrete steps, the DNA tail and the connected protein toward the enzyme through the flow path.
9. The method of claim 8 wherein a DNA structure is attached to the nanopore, the DNA structure configured to maintain separation between the enzyme and the nanopore.
10. The method of claim 1 wherein the property of the protein is at least one of: an identity of the protein and an amino acid residue sequence of the protein.
11. A system for performing single molecule proteomics, the system comprising:
a structure defining an interior cavity and a barrier dividing the interior cavity into a first chamber and a second chamber, the barrier containing a channel structure defining a nanopore therethrough fluidically coupling the first and second chambers, the nanopore having a flow path bounded by an interior surface of the channel structure, wherein the fluid includes (i) a protein comprising amino acid residues and, (ii) an agent, the agent, wherein particles of the agent are bound the interior surface of the channel structure defining the nanopore, the bound particles cause the amino acid residues of the protein that pass through the flow path of the nanopore to orient themselves as a linear series of amino acid residues;
a voltage source configured to apply a voltage gradient between the first and second chambers via the flow path, the voltage gradient inducing an ionic flow through the flow path of the nanopore;
a detector configured to observe an electronic signature produced by interactions between ions comprising the ionic flow and the linear series of amino acid residues of the protein passing through the flow path of the nanopore altering the ionic current through the flow path of the nanopore; and
a processor configured to determine a property of the protein based on the electronic signature.
12. The system of claim 11 wherein the agent includes guanidinium ions.
13. The system of claim 11 wherein the channel structure is at least one of a membrane protein and a solid-state nanopore.
14. The system of claim 11 wherein the protein is connected to a charged tail configured to guide the protein into the flow path when the voltage gradient is applied.
15. The system of claim 11 wherein the first chamber includes an enzyme that unfolds the protein.
16. The system of claim 15 wherein the enzyme that unfolds the protein is unfoldase.
17. The system of claim 11 , wherein the voltage gradient is a first voltage gradient, and wherein:
the protein is connected to a DNA tail;
the voltage source is further configured to apply a second voltage gradient between the first and the second chambers via the flow path, the second voltage gradient of sufficient strength to cause a section of the DNA tail to pass through the nanopore prior to the voltage source applying the first voltage gradient; and
the first chamber of the structure contains an enzyme, capable of drawing, in discrete steps, the DNA tail and the connected protein toward the enzyme through the flow path.
18. The system of claim 17 wherein the DNA tail comprises of a front portion of single-stranded DNA, a middle portion of double-stranded DNA, and a back portion of single-stranded DNA, wherein the front portion of single-strand DNA is the section of the DNA tail passed through the nanopore prior to the voltage source applying the first voltage gradient.
19. The system of claim 17 further comprising a DNA structure attached to the nanopore, the DNA structure configured to maintain separation between the enzyme and the nanopore.
20. The system of claim 11 wherein the property of the protein is at least one of an identity of the protein and an amino acid residue sequence of the protein.