IP Library Granted Patent US 10,882,892
Granted Patent B2
US 10,882,892 · App. 14/817,335 · Granted Jan 5, 2021

Channelrhodopsin variants and uses thereof

Inventors: Nathan Klapoetke (Ashburn, VA); Brian Yichiun Chow (Cherry Hill, NJ); Edward Boyden (Chestnut Hill, MA); Gane Ka-Shu Wong (Edmonton, CA); Yongku Peter Cho (Vernon, CT)
Assignees: Massachusetts Institute of Technology; The Governors of The University of Alberta
C07K14/705A61K38/16A61K41/00A61N5/0613C07K14/43581G01N33/6872A61K38/00A61N5/062G01N2333/705
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Quick Facts
Patent No.
US 10,882,892
App. No.
14/817,335
Granted
Jan 5, 2021
Kind
B2
Abstract

CsChrimson light-activated ion channel polypeptides, their encoding polynucleotides, and variants thereof are provided. Methods of introducing and using CsChrimson light activated ion channels and variants thereof for to alter cell activity and function are also provided.

Claims (34)

1. A CsChrimson light-activated ion channel polypeptide comprising (a) the amino acid sequence set forth as SEQ ID NO: 1 or (b) the amino acid sequence of SEQ ID NO: 1 with one, two, three, or more amino acid sequence modifications within the sequence, and having at least 97% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having at least 97% identity to amino acids 80-315 of SEQ ID NO: 1, wherein the CsChrimson light-activated ion channel polypeptide is capable of being activated with light, and the activation alters ion conductivity of the CsChrimson light-activated ion channel polypeptide.

2. A membrane comprising the CsChrimson light-activated ion channel polypeptide of claim 1 .

3. The membrane of claim 2 , wherein the membrane is a mammalian cell membrane.

4. The membrane of claim 3 , wherein the membrane is a cell membrane of a neuronal cell, a nervous system cell, a cardiac cell, a circulatory system cell, a visual system cell, or an auditory system cell.

5. A cell comprising the CsChrimson light-activated ion channel polypeptide of claim 1 .

6. The cell of claim 5 , wherein the cell is an excitable cell.

7. The cell of claim 6 , wherein activating the CsChrimson light-activated ion channel polypeptide depolarizes the cell.

8. The cell of claim 5 , wherein the cell is in a subject.

9. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 97% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 98% identity to amino acids 80-315 of SEQ ID NO: 1.

10. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 97% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 99% identity to amino acids 80-315 of SEQ ID NO: 1.

11. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 98% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 97% identity to amino acids 80-315 of SEQ ID NO: 1.

12. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 98% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 98% identity to amino acids 80-315 of SEQ ID NO: 1.

13. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 98% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 99% identity to amino acids 80-315 of SEQ ID NO: 1.

14. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 98% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 100% identity to amino acids 80-315 of SEQ ID NO: 1.

15. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 100% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 97% identity to amino acids 80-315 of SEQ ID NO: 1.

16. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 100% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 98% identity to amino acids 80-315 of SEQ ID NO: 1.

17. The CsChrimson light-activated ion channel polypeptide of claim 1 , having at least 100% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having 99% identity to amino acids 80-315 of SEQ ID NO: 1.

18. A method of altering ion conductivity of a membrane, the method comprising,

a) expressing in a host membrane a CsChrimson light-activated ion channel polypeptide comprising (a) the amino acid sequence set forth as SEQ ID NO: 1 or (b) the amino acid sequence of SEQ ID NO: 1 with one, two, three, or more amino acid sequence modifications within the sequence, and having at least 97% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having at least 97% identity to amino acids 80-315 of SEQ ID NO: 1, and wherein the CsChrimson light-activated ion channel polypeptide is capable of being activated with light, and the activation alters ion conductivity of the CsChrimson light-activated ion channel polypeptide; and

b) contacting the CsChrimson light-activated ion channel polypeptide with a light under suitable conditions to activate the light-activated ion channel and alter the ion conductivity of the membrane.

19. The method of claim 18 , wherein the host membrane is a cell membrane.

20. The method of claim 18 , wherein the membrane is a cell membrane of a neuronal cell, a nervous system cell, a cardiac cell, a circulatory system cell, a visual system cell, or an auditory system cell.

21. The method of claim 18 , wherein the CsChrimson light-activated ion channel polypeptide has at least 97% identity to amino acids 1-79 of SEQ ID NO: 1 and 98% identity to amino acids 80-315 of SEQ ID NO: 1.

22. The method of claim 18 , wherein the host membrane is in a cell.

23. The method of claim 22 , wherein the cell is a human cell.

24. The method of claim 22 , wherein altering the ion conductivity of the membrane depolarizes the cell.

25. A method of assessing the effect of a candidate compound on ion conductivity of a membrane, the method comprising,

a) contacting a test membrane comprising a light-activated ion channel polypeptide comprising (a) the amino acid sequence set forth as SEQ ID NO: 1 or (b) the amino acid sequence of SEQ ID NO: 1 with one, two, three, or more amino acid sequence modifications within the sequence, and having at least 97% identity to amino acids 1-79 of SEQ ID NO: 1 and a seven-transmembrane-domain region having at least 97% identity to amino acids 80-315 of SEQ ID NO: 1, and wherein the CsChrimson light-activated ion channel polypeptide is capable of being activated with light, and the activation alters ion conductivity of the CsChrimson light-activated ion channel polypeptide, with light under conditions suitable for altering ion conductivity of the test membrane;

b) contacting the test membrane with a candidate compound; and

c) identifying the presence or absence of a change in ion conductivity of the test membrane contacted with the light and the candidate compound compared to ion conductivity of with “a control test membrane comprising the light-activated ion channel polypeptide contacted with light, and not contacted with the candidate compound;

wherein a change in the ion conductivity of the test membrane compared to the control indicates an effect of the candidate compound on the ion conductivity of the test membrane.

26. The method of claim 25 , wherein the CsChrimson light-activated ion channel polypeptide has at least 97% identity to amino acids 1-79 of SEQ ID NO: 1 and 98% identity to amino acids 80-315 of SEQ ID NO: 1.

27. The method of claim 25 , wherein the membrane is in a cell.

28. The method of claim 27 , wherein altering the ion conductivity of the membrane depolarizes the cell.

Assignments (4)
CONFIRMATORY LICENSE Recorded Aug 3, 2016
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039551/0320 →
CONFIRMATORY LICENSE Recorded Jul 19, 2016
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039389/0468 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2016
From: KLAPOETKE, NATHAN; CHOW, BRIAN YICHIUN; BOYDEN, EDWARD; CHO, YONGKU PETER
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 038437/0347 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2016
From: WONG, GANE KA-SHU
To: THE GOVERNORS OF THE UNIVERSITY OF ALBERTA
Reel/Frame 038437/0392 →
Continuity (2)
Provisional Application 62033213 · Aug 5, 2014
Related Publication 20160039902A1 · Feb 11, 2016