MSP nanopores and related methods
Provided herein are Mycobacterium smegmatis porin nanopores, systems that comprise these nanopores, and methods of using and making these nanopores. Such nanopores may be wild-type MspA porins, mutant MspA porins, wild-type MspA paralog porins, wild-type MspA homolog porins, mutant MspA paralog porins, mutant MspA homolog porins, or single-chain Msp porins. Also provided are bacterial strains capable of inducible Msp porin expression.
1. A method of detecting a nucleic acid, the method comprising:
translocating a nucleic acid from a first conductive liquid medium to a second conductive liquid medium in liquid communication through a mutant Mycobacterium smegmatis porin A (MspA), wherein the mutant MspA comprises a mutant MspA monomer with at least one mutation with respect to SEQ ID NO:1, and wherein the mutant MspA has a neutral constriction zone;
measuring an ion current between the first conductive liquid medium and the second conductive liquid medium, wherein a 5% or more reduction in the ion current for at least 1.0 μs compared to an ion current level for the mutant MspA without the nucleic acid indicates the presence of the nucleic acid in the first medium.
2. The method of claim 1 , wherein the mutant MspA comprises a mutant MspA monomer, wherein the mutant MspA monomer comprises the following mutations of SEQ ID NO:1: D90N, D91N, and D93N.
3. The method of claim 1 , wherein the mutant MspA comprises a mutant MspA monomer, wherein the mutant MspA monomer comprises the following mutations of SEQ ID NO:1: D90N, D91N, D93N, D118R, D134R, and E139K.
4. The method of claim 1 , wherein the mutant MspA comprises a mutant MspA monomer, wherein the mutant MspA monomer comprises the following mutations of SEQ ID NO:1: D90N/Q/Y, D91N/Q/Y, and D93N/Q.
5. The method of claim 1 , wherein the mutant MspA comprises a mutant MspA monomer, wherein the mutant MspA monomer comprises one or more of the following mutations of SEQ ID NO:1: L88W, I105W, N108W, D118R, D134R, A138P, and E139A/K.
6. The method of claim 1 , wherein the mutant MspA comprises a mutant MspA monomer, wherein the mutant MspA monomer comprises one or more of the following mutations of SEQ ID NO:1: D90N/Q/Y, D91N/Q/Y, and D93N/Q.
7. The method of claim 1 , wherein the mutant MspA comprises a mutant MspA monomer, wherein the mutant MspA monomer comprises one or more mutations at the following amino acid positions of SEQ ID NO:1: 88, 105, 108, 118, 134, or 139.
8. The method of claim 1 , wherein translocating the nucleic acid from the first conductive liquid medium to the second conductive liquid medium in liquid communication through the mutant MspA comprises using a molecular motor to regulate a rate of translocation for the nucleic acid translocating through the mutant MspA.
9. The method of claim 8 , wherein the molecular motor is a helicase.
10. The method of claim 8 , wherein the molecular motor is a polymerase.
11. The method of claim 8 , wherein the nucleic acid has an average translocation velocity through the mutant MspA of less than 1 nucleotide/μs.
12. The method of claim 1 , wherein the mutant MspA comprises a mutant MspA monomer, wherein the mutant MspA monomer comprises a mutation of SEQ ID NO:1 at amino acid position 88.
13. The method of claim 1 , wherein the mutant MspA comprises a mutant MspA monomer, wherein the mutant MspA monomer comprises a mutation of SEQ ID NO:1 at amino acid position 126.
14. The method of claim 1 , wherein the mutant MspA comprises a first mutant MspA monomer comprising a mutant MspA monomer with at least one mutation with respect to SEQ ID NO:1 and a second mutant MspA monomer comprising a mutant MspA monomer with at least one mutation with respect to SEQ ID NO:1, wherein the first mutant MspA monomer has a different amino acid sequence than the second mutant MspA monomer.
15. The method of claim 1 , wherein the mutant MspA comprises a first mutant MspA monomer comprising a mutant MspA monomer with at least one mutation with respect to SEQ ID NO:1 and a second mutant MspA monomer comprising a mutant MspA monomer with at least one mutation with respect to SEQ ID NO:1, wherein the first mutant MspA monomer is connected to the second mutant MspA monomer by one or more amino acid linkers.