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公开(公告)号:US12234445B2
公开(公告)日:2025-02-25
申请号:US17293832
申请日:2019-12-26
Applicant: Calysta, Inc.
Inventor: Renee M. Saville , Joshua A. Silverman , Vincent Tang , Eric G. Luning , Paloma Rueda , Megan Hsi , Yelena Stegantseva
Abstract: The present disclosure provides methanotrophic bacteria that are modified to produce less glycogen, and methods of using the modified methanotrophic bacteria to produce a desired product, such as protein(s) or metabolite(s).
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公开(公告)号:US12234272B2
公开(公告)日:2025-02-25
申请号:US17709296
申请日:2022-03-30
Applicant: Ferring B.V.
Inventor: Ian Cottingham , Daniel Plaksin , Richard White
IPC: C07K14/575 , A61K38/16 , C07K14/59 , C12P21/00
Abstract: Described are pharmaceutical compositions comprising recombinant human chorionic gonadotropin (hCG) and optionally follicle stimulating hormone (FSH), wherein the recombinant hCG in the composition comprises α2,3- and α2,6-sialylation and comprises mono-(1S), di-(2S), tri-(3S) and tetra-(4S) sialylated glycan structures. The recombinant hCG may be obtained by expression in a human cell line, such as the PER.C6 cell line, optionally wherein the cell line is modified using α2,3-sialyltransferase.
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公开(公告)号:US12227782B2
公开(公告)日:2025-02-18
申请号:US17252010
申请日:2019-06-27
Applicant: Kao Corporation
Inventor: Nozomu Shibata , Toshiharu Arai
Abstract: Provided is an inexpensive and efficient microbiological method for producing a protein. The method for producing a protein comprises culturing a microorganism in the presence of glycosylamine.
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公开(公告)号:US12227757B2
公开(公告)日:2025-02-18
申请号:US17817966
申请日:2022-08-05
Applicant: Factor Bioscience Inc.
Inventor: Matthew Angel , Christopher Rohde
IPC: C12N15/85 , A61K35/28 , C08K5/5399 , C12N5/074 , C12N5/077 , C12N5/0789 , C12N9/16 , C12N9/22 , C12N15/87 , C12N15/90 , C12P21/00 , H01L31/048 , A61K35/12 , C08G77/08
Abstract: The present invention relates in part to nucleic acids encoding proteins, nucleic acids containing non-canonical nucleotides, therapeutics comprising nucleic acids, methods, kits, and devices for inducing cells to express proteins, methods, kits, and devices for transfecting, gene editing, and reprogramming cells, and cells, organisms, and therapeutics produced using these methods, kits, and devices. Methods for inducing cells to express proteins and for reprogramming and gene-editing cells using RNA are disclosed. Methods for producing cells from patient samples, cells produced using these methods, and therapeutics comprising cells produced using these methods are also disclosed.
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公开(公告)号:US12227723B2
公开(公告)日:2025-02-18
申请号:US18162774
申请日:2023-02-01
Applicant: Lonza Ltd
Inventor: Michael Mietzner , Rajesh Beri , Edward Gunderson
Abstract: A variable diameter bioreactor vessel is provided that includes a first vessel section having a first diameter configured to hold a liquid media and biologic material, and a second vessel section having a second diameter that is greater than the first diameter such that the liquid media can be increased from a first volume to a second volume within the vessel.
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公开(公告)号:US20250051820A1
公开(公告)日:2025-02-13
申请号:US18719514
申请日:2022-12-27
Applicant: DENKA COMPANY LIMITED
Inventor: Tomohiro NARAHARA , Ryotaro MITSUMATA
Abstract: A method for producing a protein expressed with excellent efficiency in the baculovirus expression system. A method for producing a protein in a baculovirus expression system, including a step of adding a calcium salt to a culture medium after a recombinant baculovirus is inoculated into an insect cell.
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公开(公告)号:US20250051422A1
公开(公告)日:2025-02-13
申请号:US18507236
申请日:2023-11-13
Applicant: Shandong D-nutrimec Biomedical Co., Ltd.
Inventor: Zhidong GUO , Jiajia SHAO , Hongwei MA , Huawei AI
Abstract: Provided are a recombinant collagen, an expression method and use thereof. In the present disclosure, the recombinant collagen is expressed by a human embryonic kidney cell Expi293F at a high protein expression level, thereby realizing the expression of a large-molecular-weight recombinant collagen. Activity studies have showed that the expressed recombinant collagen has desirable activity in promoting cell migration, while the recombinant collagen III+I with a fusion tag shows high stability at 4° C. In addition, cell activity studies have shown that the recombinant type III collagen expressed by human cells has better activity in promoting the cell migration than that of a commercially available type III collagen. These results indicate that the human cell expression system is conducive to the expression of highly active and large-molecular-weight recombinant collagen.
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公开(公告)号:US20250043325A1
公开(公告)日:2025-02-06
申请号:US18777939
申请日:2024-07-19
Applicant: CHO PHARMA, INC.
Inventor: WEI-SHEN WU , KUO-CHING CHU
Abstract: The present disclosure relates to a novel mutant form of α-fucosidase (α-L-fucosidase), which exhibits enhanced α-(1,6) fucosidase activity. The present disclosure also relates to the compositions comprising the novel mutant form of α-fucosidase, and the methods of using the novel mutant form of α-fucosidase to cleave α-(1,6)-linked fucoses in the glycoconjugates.
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公开(公告)号:US20250002962A1
公开(公告)日:2025-01-02
申请号:US18293313
申请日:2022-04-21
Inventor: Katharina HÖFER , Andres JÄSCHKE
IPC: C12P21/00 , C07K14/245 , C12N9/10
Abstract: The present invention relates to a method for attaching a 5′-nicotinamidnucleobasedinucleotide (NND)-capped nucleic acid sequence to a fusion protein or to a complex, comprising (a) contacting (i) a heterologous fusion protein which comprises a poly(peptide) of interest being fused to a tag, or (ii) a complex wherein a protein is under physiological conditions complexed with a tag with the 5′-NAD-capped nucleic acid sequence and an ADP-ribosyltransferase (ART) under conditions wherein the 5′-NND-capped nucleic acid sequence is covalently attached to the tag, wherein the tag comprises a recognition motif of the ART and preferably comprises or consists of (i) SEQ ID NO: 1 or a sequence being at least 80% identical thereto provided that the underlined Arg in the amino acid motif DVRPVRD (SEQ ID NO: 7) is conserved and preferably SEQ ID NO: 7 is conserved; (ii) SEQ ID NO: 2 or a sequence being at least 80% identical thereto provided that the underlined Arg in the amino acid motif DVRPVRD (SEQ ID NO: 7) is conserved and preferably SEQ ID NO: 7 is conserved; (iii) SEQ ID NO: 3 or a sequence being at least 80% identical thereto provided that the underlined Arg in the amino acid motif DVRPVRD (SEQ ID NO: 7) is conserved and preferably SEQ ID NO: 7 is conserved; (iv) SEQ ID NO: 4 or a sequence being at least 80% identical thereto provided that the underlined Arg in the amino acid motif LADGVEGYLRASEASRDRVE (SEQ ID NO: 8) is conserved and preferably SEQ ID NO: 8 is conserved; (v) SEQ ID NO: 5 or a sequence being at least 80% identical thereto provided that the underlined Arg in the amino acid motif LADGVEGYLRASEASRDRVE (SEQ ID NO: 8) is conserved and preferably SEQ ID NO: 8 is conserved; or (vi) SEQ ID NO: 6 or a sequence being at least 80% identical thereto provided that the underlined Arg in the amino acid motif LADGVEGYLRASEASRDRVE (SEQ ID NO: 8) is conserved and preferably SEQ ID NO: 8 is conserved.
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公开(公告)号:US20240415139A1
公开(公告)日:2024-12-19
申请号:US18703056
申请日:2022-10-20
Applicant: TECHNISCHE UNIVERSITÄT MÜNCHEN
Inventor: Mahmoud MASRI , Thomas BRÜCK , Petra GRABAN , Farah QOURA , Corinna DAWID , Ludovic GERBOIN , Melania PILZ
Abstract: The present invention relates to a method for producing microbial lipids, optionally for producing microbial lipids and protein biomass and/or aromatic compounds. The present invention further relates to a use of a microbial lipid. The present invention also relates to a composition comprising at least five enzymes.
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