Methods of treating cancer using lsd1 inhibitors in combination with immunotherapy
US-2024018242-A1 · Jan 18, 2024 · US
US9676830B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9676830-B2 |
| Application number | US-201113883923-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 18, 2011 |
| Priority date | Nov 18, 2010 |
| Publication date | Jun 13, 2017 |
| Grant date | Jun 13, 2017 |
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The present invention relates to chimeric GH61 polypeptides having cellulolytic enhancing activity. The present invention also relates to polynucleotides encoding the chimeric GH61 polypeptides; nucleic acid constructs, vectors, and host cells comprising the polynucleotides; and methods of using the chimeric GH61 polypeptides.
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What is claimed is: 1. An isolated chimeric GH61 polypeptide having cellulolytic enhancing activity, comprising: (a) a first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide, wherein the first GH61 polypeptide fragment is selected from the group consisting of (i) a polypeptide fragment having at least 95% sequence identity to amino acids 22 to 84 of the polypeptide of SEQ ID NO: 78; and (ii) a polypeptide fragment comprising amino acids 22 to 84 of the polypeptide of SEQ ID NO: 78; (b) a second GH61 polypeptide fragment at the C-terminal end of the first GH61 polypeptide fragment, wherein the second GH61 polypeptide fragment is selected from the group consisting of (i) a polypeptide fragment having at least 95% sequence identity to amino acids 85 to 207 of the polypeptide of SEQ ID NO: 94; and (ii) a polypeptide fragment comprising amino acids 85 to 207 of the polypeptide of SEQ ID NO: 94; and (c) a third GH61 polypeptide fragment at the C-terminal end of the second GH61 polypeptide fragment, wherein the third GH61 polypeptide fragment is selected from the group consisting of (i) a polypeptide fragment having at least 95% sequence identity to amino acids 208 to 249 of the polypeptide of SEQ ID NO: 78; and (ii) a polypeptide fragment comprising amino acids 208 to 249 of the polypeptide of SEQ ID NO: 78. 2. The chimeric GH61 polypeptide of claim 1 , wherein the first GH61 polypeptide fragment comprises amino acids 22 to 84 of the polypeptide of SEQ ID NO: 78. 3. The chimeric GH61 polypeptide of claim 1 , wherein the second GH61 polypeptide fragment comprises amino acids 85 to 207 of the polypeptide of SEQ ID NO: 94. 4. The chimeric GH61 polypeptide of claim 1 , wherein the third GH61 polypeptide fragment comprises amino acids 208 to 249 of the polypeptide of SEQ ID NO: 78. 5. The chimeric GH61 polypeptide of claim 1 , which comprises amino acids 22 to 84 of the polypeptide of SEQ ID NO: 78 as the first GH61 polypeptide fragment at the N-terminal end of the chimeric GH61 polypeptide, amino acids 85 to 207 of the polypeptide of SEQ ID NO: 94 as the second GH61 polypeptide fragment at the C-terminal end of the first GH61 polypeptide fragment, and amino acids 208 to 249 of the polypeptide of SEQ ID NO: 78 as the third GH61 polypeptide fragment at the C-terminal end of the second GH61 polypeptide fragment. 6. The chimeric GH61 polypeptide of claim 1 , which comprises the mature polypeptide of SEQ ID NO: 144. 7. An isolated polynucleotide encoding the chimeric GH61 polypeptide of claim 1 . 8. A host cell comprising the polynucleotide of claim 7 . 9. A method of producing a chimeric GH61 polypeptide having cellulolytic enhancing activity, comprising: (a) cultivating the host cell of claim 8 under conditions suitable for the expression of the chimeric GH61 polypeptide; and (b) recovering the chimeric GH61 polypeptide. 10. A transgenic plant, plant part or plant cell transformed with the polynucleotide of claim 7 encoding the chimeric GH61 polypeptide. 11. A method of producing the chimeric GH61 polypeptide of claim 1 , comprising: (a) cultivating a transgenic plant or a plant cell comprising a polynucleotide encoding the chimeric GH61 polypeptide under conditions conducive for production of the chimeric GH61 polypeptide; and (b) recovering the chimeric GH61 polypeptide. 12. A method for degrading or converting a cellulosic material, comprising: treating the cellulosic material with an enzyme composition comprising the chimeric GH61 polypeptide of claim 1 . 13. The method of claim 12 , further comprising recovering the degraded or converted cellulosic material. 14. The method of claim 12 , wherein the enzyme composition further comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, a polypeptide having cellulolytic enhancing activity, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin. 15. The method of claim 12 , wherein the converted cellulosic material is a sugar. 16. A method for producing a fermentation product, comprising: (a) saccharifying a cellulosic material with an enzyme composition comprising the chimeric GH61 polypeptide of claim 1 ; (b) fermenting the saccharified cellulosic material with one or more fermenting microorganisms to produce the fermentation product; and (c) recovering the fermentation product from the fermentation. 17. The method of claim 16 , wherein the enzyme composition further comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, a polypeptide having cellulolytic enhancing activity, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin. 18. A method of fermenting a cellulosic material, comprising: fermenting the cellulosic material with one or more fermenting microorganisms, wherein the cellulosic material is saccharified with an enzyme composition comprising the chimeric GH61 polypeptide of claim 1 . 19. The method of claim 18 , wherein the enzyme composition further comprises one or more enzymes selected from the group consisting of a cellulase, a hemicellulase, a polypeptide having cellulolytic enhancing activity, an esterase, an expansin, a laccase, a ligninolytic enzyme, a pectinase, a peroxidase, a protease, and a swollenin. 20. The method of claim 18 , wherein the fermenting of the cellulosic material produces a fermentation product. 21. The method of claim 20 , further comprising recovering the fermentation product from the fermentation. 22. A whole broth formulation or cell culture composition comprising the chimeric GH61 polypeptide of claim 1 . 23. The chimeric GH61 polypeptide of claim 1 , wherein the first GH61 polypeptide fragment has at least 96% sequence identity to amino acids 22 to 84 of the polypeptide of SEQ ID NO: 78. 24. The chimeric GH61 polypeptide of claim 1 , wherein the first GH61 polypeptide fragment has at least 97% sequence identity to amino acids 22 to 84 of the polypeptide of SEQ ID NO: 78. 25. The chimeric GH61 polypeptide of claim 1 , wherein the first GH61 polypeptide fragment has at least 98% sequence identity to amino acids 22 to 84 of the polypeptide of SEQ ID NO: 78. 26. The chimeric GH61 polypeptide of claim 1 , wherein the first GH61 polypeptide fragment has at least 99% sequence identity to amino acids 22 to 84 of the polypeptide of SEQ ID NO: 78. 27. The chimeric GH61 polypeptide of claim 1 , wherein the second GH61 polypeptide fragment has at least 96% sequence identity to amino acids 85 to 207 of the polypeptide of SEQ ID NO: 94. 28. The chimeric GH61 polypeptide of claim 1 , wherein the second GH61 polypeptide fragment has at least 97% sequence identity to amino acids 85 to 207 of the polypeptide of SEQ ID NO: 94. 29. The chimeric GH61 polypeptide of claim 1 , wherein the second GH61 polypeptide fragment has at least 98% sequence identity to amino acids 85 to 207 of the polypeptide of SEQ ID NO: 94. 30. The chimeric GH61 polypeptide of claim 1 , wherein the second GH61 polypeptide fragment has at least 99% sequence identity to amino acids 85 to 207 of the polypeptide of SEQ ID NO: 94. 31. The chimeric GH61 polypeptide of claim 1 , wherein the third GH61 polypeptide fragment has at leas
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