Modified nanopores, compositions comprising the same, and uses thereof

US11840556B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11840556-B2
Application numberUS-201816484798-A
CountryUS
Kind codeB2
Filing dateFeb 12, 2018
Priority dateFeb 10, 2017
Publication dateDec 12, 2023
Grant dateDec 12, 2023

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Provided herein relate to modified or mutant forms of secretin and compositions comprising the same. In particular, the modified or mutant forms of secretin permits efficient capture and/or translocation of an analyte through the modified or mutant secretin nanopores. Methods for using unmodified secretin or the modified or mutant forms of secretin and compositions, for example, for characterizing an analyte, e.g., a target polynucleotide, are also provided.

First claim

Opening claim text (preview).

The invention claimed is: 1. A nanopore sequencing apparatus comprising a chamber housing an aqueous solution having disposed therein a membrane comprising a modified secretin nanopore disposed in the membrane, the modified secretin nanopore comprising a lumenal surface defining a lumen that extends through the membrane between a cis-opening and a trans-opening, wherein the lumenal surface comprises one or more amino acid modifications relative to a wild-type secretin nanopore. 2. The nanopore sequencing apparatus of claim 1 , wherein the one or more amino acid modifications comprise a charge-altering modification and the charge-altering modification is a substitution of a negatively-charged amino acid with a positively-charged amino acid or the one or more amino acid modifications comprise a substitution of a neutral amino acid with a hydrophobic amino acid. 3. The nanopore sequencing apparatus of claim 1 , wherein the cis-opening has a diameter in a range of 60 Å to 120 Å, the trans-opening has a diameter in a range of 40 Å to 100 Å and the secretin nanopore comprises a constriction having a diameter of about 7.5 Å to 25 Å. 4. The nanopore sequencing apparatus of claim 1 , wherein the secretin is of a type II, type III or type IV secretion system, optionally wherein the modified secretin is GspD, YscC, InvG or PilQ. 5. The nanopore sequencing apparatus of claim 1 , which comprises a subunit polypeptide having an amino acid sequence that is at least 95% identical to the amino acid sequence as set forth in SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 1, or SEQ ID NO: 2. 6. The nanopore sequencing apparatus of claim 1 wherein the secretin is GaspD and wherein the central gate of GspD is modified to replace an amino acid with an amino acid having a smaller side group and/or to replace a negatively charged amino acid with a neutral or positively charged amino acid. 7. The nanopore sequencing apparatus of claim 1 wherein the secretin is GspD and which comprises a subunit polypeptide comprising a secretin domain having an amino acid sequence that is at least 95% identical to an amino acid sequence as set forth in SEQ ID NO: 36, wherein: (i) all or some of the amino acids from D55 or T56 to T77 are deleted or substituted, one or more of K60, D64, R71 and E73 is substituted with an uncharged amino acid and/or one or more of D55, T56, T77 and K78 is substituted with P; and/or (ii) F156 is substituted with a smaller amino acid, N151 and/or N152 is/are substituted with a smaller amino acid, D153 is substituted with an uncharged amino acid, G137 and G165 are each independently unmodified or substituted with A or V; and/or (iii)Y63 to R71 are deleted and/or substituted with GSG or SGS, F156 is substituted with A, D153 is substituted with S, and/or N151 and N152 are each independently substituted with G or S. 8. The nanopore sequencing apparatus of claim 1 , wherein the secretin is InvG or which comprises a subunit polypeptide having an amino acid sequence that is at least 95% identical to the amino acid sequence as set forth in SEQ ID NO: 1,wherein the lumenal surface further defines a constriction within the lumen, the constriction having one or more amino acid modifications at amino acids D28, E225, R226, and/or E231 of SEQ ID NO: 1, optionally comprising one or more of the following: i. D28N/Q/T/S/G/R/K; ii. E225N/Q/T/A/S/G/P/H/F/Y/R/K; iii. R226N/Q/T/A/S/G/P/H/F/Y/K/V; iv. Deletion of E225; v. Deletion of R226; and vi. E231N/Q/T/A/S/G/P/H/R/K. 9. The nanopore sequencing apparatus of claim 1 , wherein the secretin is InvG or which comprises a subunit polypeptide having an amino acid sequence that is at least 95% identical to the amino acid sequence as set forth in SEQ ID NO: 1, wherein the lumenal surface comprises a capture portion having one or more amino acid modifications at amino acids E41, Q45 or E114, optionally comprising one or more of the following amino acid modifications: i. Q45R/K; ii. E41N/Q/T/S/G/R/K; and iii. E114N/Q/T/S/G/R/K. 10. The nanopore sequencing apparatus of claim 1 , further comprising an analyte present in the aqueous solution. 11. The nanopore sequencing apparatus of claim 10 , wherein the analyte is a polynucleotide. 12. The nanopore sequencing apparatus of claim 11 , further comprising a polynucleotide binding protein bound to the polynucleotide. 13. The nanopore sequencing apparatus of claim 12 , wherein the polynucleotide binding protein is a helicase, exonuclease, or polymerase. 14. The nanopore sequencing apparatus of claim 12 , wherein the polynucleotide binding protein is on the cis-side of the membrane. 15. The nanopore sequencing apparatus of claim 14 , wherein the polynucleotide binding protein is in contact with or covalently attached to the cis-opening of the nanopore. 16. The nanopore sequencing apparatus of claim 12 , wherein the polynucleotide binding protein is on the trans-side of the membrane. 17. The nanopore sequencing apparatus of claim 16 , wherein the polynucleotide binding protein is in contact with or covalently attached to the trans-opening of the nanopore.

Assignees

Inventors

Classifications

  • Escherichia (G) · CPC title

  • Salmonella (G) · CPC title

  • C12Q1/6869Primary

    Methods for sequencing · CPC title

  • C07K14/195Primary

    from bacteria · CPC title

  • Nanotechnology for materials or surface science, e.g. nanocomposites · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11840556B2 cover?
Provided herein relate to modified or mutant forms of secretin and compositions comprising the same. In particular, the modified or mutant forms of secretin permits efficient capture and/or translocation of an analyte through the modified or mutant secretin nanopores. Methods for using unmodified secretin or the modified or mutant forms of secretin and compositions, for example, for characteriz…
Who is the assignee on this patent?
Oxford Nanopore Tech Plc
What technology area does this patent fall under?
Primary CPC classification C12Q1/6869. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).