Nanopore device for drug-like molecule screening or lead optimization to a targeted protein
A nanosensor for detecting molecule characteristics includes a membrane having an opening configured to permit a charged molecule to pass but to block a protein molecule attached to a ligand connecting to the charged molecule, the opening being filled with an electrolytic solution. An electric field generator is configured to generate an electric field relative to the opening to drive the charged molecule through the opening. A sensor circuit is coupled to the electric field generator to sense current changes due to charged molecules passing into the opening. The current changes are employed to trigger a bias field increase to cause separation between the ligand and the protein to infer an interaction strength.
1. A method for detecting a protein molecule characteristics, comprising:
generating an electric field across a membrane having an opening to drive a charged carbon nanotube molecule through the opening, the charged carbon nanotube being connected to a ligand, the ligand being bonded to the protein molecule, the opening being configured to permit the charged nanotube to pass but to block the protein molecule attached to the charged nanotube, the opening being filled with an electrolytic solution;
sensing current changes due to the charged carbon nanotube passing into or through the opening;
biasing the electric field to cause a separation between the ligand and the protein molecule; and
correlating a voltage at the separation to measure a characteristic of the protein molecule to ligand interaction.
2. The method as recited in claim 1 , wherein the opening includes one of a nanopore and a channel.
3. The method as recited in claim 1 , wherein sensing includes measuring current drops and durations to determine a blockage in the opening.
4. The method as recited in claim 1 , wherein the characteristic includes an affinity between the ligand and the protein molecule.
5. The method as recited in claim 1 , wherein the charged carbon nanotube includes a closed functionalized end having charged chemical groups.
6. The method as recited in claim 1 , wherein biasing the electric field includes increasing a biasing value to determine a critical voltage value at which separation occurs between the charged carbon nanotube and the protein molecule to infer interaction strength.
7. A method for detecting a protein molecule characteristics, comprising:
generating an electric field across a membrane haying an opening to drive a charged nanowire through the opening, the charged nanowire being connected to a ligand, the ligand being bonded to the protein molecule, the opening being configured to permit the charged nanowire to pass but to block the protein molecule attached to the charged nanowire, the opening being filled with an electrolytic solution;
sensing current changes due to the charged nanowire passing into or through the opening,
biasing the electric field to cause a separation between the ligand and the protein molecule; and
correlating a voltage at the separation to measure a characteristic of the protein molecule to ligand interaction.