HRP20211748T1 - Postupci i sastavi za sekreciju heterolognih polipeptida - Google Patents
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- HRP20211748T1 HRP20211748T1 HRP20211748TT HRP20211748T HRP20211748T1 HR P20211748 T1 HRP20211748 T1 HR P20211748T1 HR P20211748T T HRP20211748T T HR P20211748TT HR P20211748 T HRP20211748 T HR P20211748T HR P20211748 T1 HRP20211748 T1 HR P20211748T1
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- 229920001184 polypeptide Polymers 0.000 title claims 25
- 108090000765 processed proteins & peptides Proteins 0.000 title claims 25
- 102000004196 processed proteins & peptides Human genes 0.000 title claims 25
- 238000000034 method Methods 0.000 title claims 12
- 230000028327 secretion Effects 0.000 title claims 3
- 239000000203 mixture Substances 0.000 title 1
- 108010076504 Protein Sorting Signals Proteins 0.000 claims 42
- 102000040430 polynucleotide Human genes 0.000 claims 31
- 108091033319 polynucleotide Proteins 0.000 claims 31
- 239000002157 polynucleotide Substances 0.000 claims 31
- 210000004027 cell Anatomy 0.000 claims 21
- 230000035772 mutation Effects 0.000 claims 13
- 101000867232 Escherichia coli Heat-stable enterotoxin II Proteins 0.000 claims 10
- 241000588724 Escherichia coli Species 0.000 claims 9
- 108010006519 Molecular Chaperones Proteins 0.000 claims 4
- 102000005431 Molecular Chaperones Human genes 0.000 claims 4
- 108091005804 Peptidases Proteins 0.000 claims 4
- 239000004365 Protease Substances 0.000 claims 4
- 101100084022 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) lapA gene Proteins 0.000 claims 4
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims 4
- 230000000694 effects Effects 0.000 claims 4
- 101150009573 phoA gene Proteins 0.000 claims 4
- 108090000623 proteins and genes Proteins 0.000 claims 4
- 102200158393 rs5030732 Human genes 0.000 claims 4
- 102220558029 Glutathione hydrolase 5 proenzyme_L11I_mutation Human genes 0.000 claims 3
- 102000008394 Immunoglobulin Fragments Human genes 0.000 claims 3
- 108010021625 Immunoglobulin Fragments Proteins 0.000 claims 3
- 101100178822 Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) htrA1 gene Proteins 0.000 claims 3
- 101100277437 Rhizobium meliloti (strain 1021) degP1 gene Proteins 0.000 claims 3
- 101150018266 degP gene Proteins 0.000 claims 3
- 102000039446 nucleic acids Human genes 0.000 claims 3
- 108020004707 nucleic acids Proteins 0.000 claims 3
- 150000007523 nucleic acids Chemical class 0.000 claims 3
- 230000002950 deficient Effects 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 102220054627 rs45495192 Human genes 0.000 claims 2
- -1 tac Proteins 0.000 claims 2
- 239000013598 vector Substances 0.000 claims 2
- 102220479740 Cell division cycle protein 123 homolog_S11I_mutation Human genes 0.000 claims 1
- 101150081864 Spr gene Proteins 0.000 claims 1
- 238000004113 cell culture Methods 0.000 claims 1
- 239000006143 cell culture medium Substances 0.000 claims 1
- 238000012258 culturing Methods 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 239000013604 expression vector Substances 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 210000001236 prokaryotic cell Anatomy 0.000 claims 1
- 102200048773 rs2224391 Human genes 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/62—DNA sequences coding for fusion proteins
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/62—DNA sequences coding for fusion proteins
- C12N15/625—DNA sequences coding for fusion proteins containing a sequence coding for a signal sequence
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/70—Vectors or expression systems specially adapted for E. coli
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
- C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/10—Immunoglobulins specific features characterized by their source of isolation or production
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/10—Immunoglobulins specific features characterized by their source of isolation or production
- C07K2317/14—Specific host cells or culture conditions, e.g. components, pH or temperature
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/31—Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
- C07K2319/02—Fusion polypeptide containing a localisation/targetting motif containing a signal sequence
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2800/00—Nucleic acids vectors
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Biomedical Technology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Microbiology (AREA)
- Plant Pathology (AREA)
- Physics & Mathematics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Immunology (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Claims (23)
1. Postupak za povećanje sekrecije teškog lanca protutijela i/ili lakog lanca protutijela iz stanice domaćina E. coli, naznačen time, da obuhvaća uzgoj stanice domaćina E. coli koja sadrži polinukleotid koji sadrži
(1) prvi polinukleotid koji kodira prvi signalni peptid operabilno povezan s polinukleotidom koji kodira teški lanac protutijela, pri čemu je prosječna hidrofobnost signalnog peptida veća od oko 0,5; i
(2) drugi polinukleotid koji kodira drugi signalni peptid koji je operabilno povezan s polinukleotidom koji kodira laki lanac protutijela, pri čemu je prosječna hidrofobnost drugog signalnog peptida veća od oko 0,5, pri čemu se, nakon ekspresije protutijela u stanici domaćina, teški i laki lanci nabiru i grupiraju tako da tvore biološki aktivno protutijelo,
pri čemu su prvi i drugi signalni peptid varijanta signalnog peptida DsbA, pri čemu varijanta signalnog peptida DsbA sadrži
a) mutaciju na ostatku L11 i/ili S18Y slijeda SEQ ID NO: 3, pri čemu varijanta signalnog peptida DsbA ima veću prosječnu hidrofobnost od signalnog peptida DsbA divljeg tipa slijeda SEQ ID NO: 3, koji ima prosječnu hidrofobnost 0,50; ili
b) mutaciju na ostatku L11 i/ili S18Y, pri čemu mutacija na ostatku L11 je L11I i pri čemu varijanta signalnog peptida DsbA ima veću prosječnu hidrofobnost od signalnog peptida DsbA divljeg tipa slijeda SEQ ID NO: 3, koji ima prosječnu hidrofobnost 0,50; ili
c) slijed SEQ ID NO: 13 ili 15.
2. Postupak prema patentnom zahtjevu 1, naznačen time, da
a) polinukleotid u stanici domaćinu nadalje sadrži promotor; ili
b) polinukleotid u stanici domaćinu nadalje sadrži promotor, pri čemu je promotor prokariotski promotor odabran iz skupine koju čine phoA, tac, lpp, lac-lpp, lac, ara i T7 promotor.
3. Postupak prema bilo kojem od patentnih zahtjeva od 1 do 2, naznačen time, da je stanica domaćin E. coli soja deficijentnog
a) u endogenim proteaznim aktivnostima, ili
b) u endogenim proteaznim aktivnostima, pri čemu genotipu E. coli nedostaju geni degP i prc, a nosi mutirani gen spr.
4. Postupak prema bilo kojem od patentnih zahtjeva od 1 do 3, naznačen time, da stanica domaćin nadalje sadrži polinukleotid koji kodira najmanje jedan prokariotski polipeptid odabran iz skupine koju čine
a) DsbA, DsbC, DsbG i FkpA, ili
b) DsbA, DsbC, DsbG i FkpA, pri čemu polinukleotid kodira i DsbA i DsbC.
5. Postupak prema bilo kojem od patentnih zahtjeva od 1 do 4, naznačen time, da je protutijelo
a) monoklonsko protutijelo; ili
b) monoklonsko protutijelo, pri čemu je monoklonsko protutijelo kimerno protutijelo, protutijelo s afinitetnom maturacijom, bispecifično, humanizirano ili humano protutijelo.
6. Varijantni signalni peptid DsbA koji sadrži mutaciju na ostatku L11 i/ili S18Y slijeda SEQ ID NO: 3, pri čemu varijanta ima
a) veću prosječnu hidrofobnost od signalnog peptida DsbA slijeda SEQ ID NO: 3, koji ima prosječnu hidrofobnost 0,50; ili
b) veću prosječnu hidrofobnost od signalnog peptida DsbA slijeda SEQ ID NO: 3, koji ima prosječnu hidrofobnost 0,50, i pri čemu mutacija na ostatku L11 je L11I.
7. Varijantni signalni peptid STII koji sadrži mutaciju u ostatku S11 slijeda SEQ ID NO: 1, pri čemu varijantni signalni peptid STII ima
a) veću prosječnu hidrofobnost od signalnog peptida STII slijeda SEQ ID NO: 1, koji ima prosječnu hidrofobnost 0,40;
b) veću prosječnu hidrofobnost od signalnog peptida STII slijeda SEQ ID NO: 1, koji ima prosječnu hidrofobnost 0,40, i pri čemu je mutacija S11 A, S11I ili S11L.
8. Varijantni signalni peptid koji se sastoji od slijeda SEQ ID NO: 8, 11, 13, 15, 31 ili 33.
9. Varijantni signalni peptid prema bilo kojem od patentnih zahtjeva od 6 do 7, spojen s
a) heterolognim proteinom, ili
b) heterolognim proteinom, pri čemu je heterologni polipeptid
i) teški lanac protutijela; ili
ii) laki lanac protutijela; ili
iii) laki i teški lanac protutijela; ili
iv) multimerni polipeptid; ili
v) imunoadhezin.
10. Polinukleotidni slijed koji kodira varijantni signalni peptid prema bilo kojem od patentnih zahtjeva od 6 do 7.
11. Polinukleotidni slijed prema patentnom zahtjevu 10 operabilno povezan s polinukleotidom koji kodira heterologni polipeptid, pri čemu se nakon ekspresije heterolognog polipeptida u stanici domaćina heterologni polipeptid nabire i grupira tako da tvori
a) biološki aktivan heterologni polipeptid; ili
b) biološki aktivan heterologni polipeptid, pri čemu je stanica domaćin
i) prokariotska stanica domaćin; ili
ii) E. coli.
12. Polinukleotid koji kodira protutijelo, pri čemu navedeni polinukleotid sadrži (1) polinukleotid koji kodira prvi signalni peptid operabilno povezan s polinukleotidom koji kodira teški lanac protutijela i (2) polinukleotid koji kodira drugi signalni peptid koji je operabilno povezan s polinukleotidom koji kodira laki lanac protutijela, pri čemu se nakon ekspresije protutijela u stanici domaćina teški i laki lanci nabiru i grupiraju tako da tvore biološki aktivno protutijelo, pri čemu
a) prvi i/ili drugi signalni peptid je varijantni signalni peptid prema patentnom zahtjevu 6 ili 7, ili naznačen time, da se prvi i/ili drugi signalni peptid sastoji od ili sadrži slijed SEQ ID NO: 8, 11, 13, 15, 31 ili 33; ili
b) prvi i/ili drugi signalni peptid je varijantni signalni peptid prema patentnom zahtjevu 6 ili 7, ili naznačen time, da se prvi i/ili drugi signalni peptid sastoji od ili sadrži slijed SEQ ID NO: 8, 11, 13, 15, 31 ili 33, pri čemu polinukleotid koji kodira protutijelo nadalje sadrži (3) polinukleotid koji kodira treći signalni peptid operabilno povezan s polinukleotidom koji kodira Fc polipeptid, pri čemu je treći signalni peptid
i) varijantni signalni peptid DsbA slijeda SEQ ID NO: 3, pri čemu varijanta sadrži H regiju prosječne hidrofobnosti veće od 0,5; ili
ii) varijantni signalni peptid DsbA koji sadrži mutaciju na ostatku L11 i/ili S18 slijeda SEQ ID NO: 3, pri čemu varijanta ima veću prosječnu hidrofobnost od signalnog peptida DsbA slijeda SEQ ID NO: 3, koji ima prosječnu hidrofobnost 0,50; ili
iii) varijantni signalni peptid DsbA koji sadrži mutaciju na ostatku L11 i/ili S18 slijeda SEQ ID NO: 3, pri čemu varijanta ima veću prosječnu hidrofobnost od signalnog peptida DsbA slijeda SEQ ID NO: 3, koji ima prosječnu hidrofobnost 0,50, pri čemu je mutacija L11I i/ili S18Y; ili
iv) varijantni signalni peptid STII koji sadrži mutaciju u ostatku S11 slijeda SEQ ID NO: 1, pri čemu varijanta signalnog peptida STII ima veću prosječnu hidrofobnost od signalnog peptida STII slijeda SEQ ID NO: 1, koji ima prosječnu hidrofobnost 0,40; ili
v) varijantni signalni peptid STII koji sadrži mutaciju u ostatku S11 slijeda SEQ ID NO: 1, pri čemu varijantni signalni peptid STII ima veću prosječnu hidrofobnost od signalnog peptida STII slijeda SEQ ID NO: 1, koji ima prosječnu hidrofobnost 0,40, pri čemu je mutacija S11A, Sill ili S11L; ili
vi) se sastoji ili sadrži slijed SEQ ID NO: 8, 11, 13, 15, 31 ili 33.
13. Polinukleotid prema bilo kojem od patentnih zahtjeva od 11 do 12, koji nadalje sadrži promotor operabilno povezan s
a) heterolognim polipeptidom; ili
b) heterolognim polipeptidom, pri čemu je promotor prokariotski promotor odabran iz skupine koju čine phoA, tac, lpp, lac-lpp, lac, ara, trp i T7 promotor.
14. Polinukleotid prema bilo kojem od patentnih zahtjeva od 11 do 13, koji nadalje sadrži (a) prvi promotor, pri čemu je prvi promotor operabilno povezan s lakim lancem i (b) drugi promotor, pri čemu je drugi promotor operabilno povezan s
a) teškim lancem; ili
b) teškim lancem, pri čemu su prvi i drugi promotor oba phoA promotori.
15. Polinukleotid prema patentnom zahtjevu 14, koji nadalje sadrži (c) treći promotor, naznačen time, da je treći promotor operabilno povezan s
a) Fc polipeptidom, ili
b) Fc polipeptidom, pri čemu je treći promotor phoA promotor.
16. Polinukleotid prema bilo kojem od patentnih zahtjeva od 12 do 15, naznačen time, da je protutijelo
a) monoklonsko protutijelo; ili
b) monoklonsko protutijelo, pri čemu je protutijelo kimerno protutijelo, bispecifično protutijelo, humanizirano protutijelo, fragment protutijela ili humano protutijelo; ili
c) fragment protutijela, naznačen time, da je fragment protutijela jednokrako protutijelo.
17. Vektor, naznačen time, da sadrži
a) polinukleotid prema bilo kojem od patentnih zahtjeva od 11 do 16; ili
b) polinukleotid prema bilo kojem od patentnih zahtjeva od 11 do 16, naznačen time, da je vektor ekspresijski vektor.
18. Stanica domaćin kojasadrži
a) polinukleotid prema patentnim zahtjevima od 10 do 16; ili
b) polinukleotid prema patentnim zahtjevima od 10 do 16, naznačena time, da je stanica domaćin
i) prokariotska stanica; ili
ii) E. coli, pri čemu, opcionalno, genotipu E. coli nedostaju geni degP i prc, a nosi mutirani gen spr; ili
iii) E. coli soja deficijentnog u i) endogenim proteaznim aktivnostima; ili ii) endogenim proteaznim aktivnostima, pri čemu genotipu E. coli nedostaju geni degP i prc, a nosi mutirani gen spr.
19. Stanica domaćin prema patentnom zahtjevu 18, naznačena time, da stanica domaćin
a) nadalje sadrži polinukleotid koji kodira i) prokariotski protein šaperon; ili ii) prokariotski protein šaperon, pri čemu je prokariotski protein šaperon DsbA i/ili DsbC; i/ili
b) pri čemu stanica domaćin prekomjerno eksprimira prokariotski protein šaperon.
20. Postupak za dobivanje heterolognog polipeptida (kao što je teški lanac i/ili laki lanac protutijela), naznačen time, da obuhvaća uzgoj stanice domaćina prema bilo kojem od patentnih zahtjeva od 18 do 19, na način da se eksprimira nukleinska kiselina, pri čemu se, nakon ekspresije navedenog polinukleotida u stanici domaćinu, heterologni polipeptid nabire tako da tvori biološki aktivan heterologni polipeptid.
21. Postupak prema patentnom zahtjevu 20, naznačen time, da postupak nadalje obuhvaća
a) dobivanje heterolognog polipeptida iz i) uzgoja stanice domaćina; ili ii) uzgoja stanice domaćina, pri čemu je heterologni polipeptid dobiven iz medija uzgoja stanice domaćina; i/ili
b) kombiniranje dobivenog heterolognog polipeptida s farmaceutski prihvatljivim nosačem, pomoćnom tvari ili nosačem za pripravu farmaceutskog pripravka koji sadrži heterologni polipeptid.
22. Postupak za sekreciju heterolognog polipeptida (kao što je teški lanac i/ili laki lanac protutijela), naznačen time, da obuhvaća uzgoj stanice domaćina prema bilo kojem od patentnih zahtjeva od 18 do 19, na način da se eksprimira nukleinska kiselina i luči heterologni polipeptid.
23. Postupak za translokaciju heterolognog polipeptida (kao što je teški lanac i/ili laki lanac protutijela) iz stanice, pri čemu navedeni postupak obuhvaća uzgoj stanice domaćina prema bilo kojem od patentnih zahtjeva od 18 do 19, na način da se eksprimira nukleinska kiselina i translocira heterologni polipeptid.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201461953629P | 2014-03-14 | 2014-03-14 | |
US201562107981P | 2015-01-26 | 2015-01-26 | |
US201562108476P | 2015-01-27 | 2015-01-27 | |
PCT/US2015/020783 WO2015139046A1 (en) | 2014-03-14 | 2015-03-16 | Methods and compositions for secretion of heterologous polypeptides |
EP15716209.0A EP3116999B1 (en) | 2014-03-14 | 2015-03-16 | Methods and compositions for secretion of heterologous polypeptides |
Publications (1)
Publication Number | Publication Date |
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HRP20211748T1 true HRP20211748T1 (hr) | 2022-02-18 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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HRP20211748TT HRP20211748T1 (hr) | 2014-03-14 | 2015-03-16 | Postupci i sastavi za sekreciju heterolognih polipeptida |
Country Status (18)
Country | Link |
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US (2) | US10435694B2 (hr) |
EP (1) | EP3116999B1 (hr) |
JP (2) | JP6644717B2 (hr) |
KR (1) | KR102561695B1 (hr) |
CN (1) | CN106103730B (hr) |
AU (1) | AU2015229035B2 (hr) |
BR (1) | BR112016020822A2 (hr) |
CA (1) | CA2941687A1 (hr) |
ES (1) | ES2897765T3 (hr) |
HR (1) | HRP20211748T1 (hr) |
IL (1) | IL247632B (hr) |
MA (1) | MA39746A (hr) |
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CN109863247A (zh) * | 2016-10-27 | 2019-06-07 | 免疫医疗有限责任公司 | 用于改善的蛋白质的分泌的信号多肽 |
CN106676122B (zh) * | 2017-01-24 | 2019-10-29 | 成都分子脉象生物科技有限公司 | 一种基于AraF信号肽的双功能DNA元件及其应用 |
GB201708277D0 (en) * | 2017-05-24 | 2017-07-05 | Ge Healthcare | A Recombinant protein |
KR101946789B1 (ko) * | 2018-01-26 | 2019-02-12 | (주)휴온스 | 이황화결합 이성질화효소 신호 펩타이드를 포함하는 재조합 벡터 및 이의 용도 |
SG11202105267VA (en) * | 2018-12-19 | 2021-07-29 | Versameb Ag | Rna encoding a protein |
KR20220031670A (ko) * | 2019-08-05 | 2022-03-11 | 와커 헤미 아게 | 발효 방법에서 재조합 단백질 방출용 박테리아 균주 |
SE543945C2 (en) * | 2020-02-07 | 2021-10-05 | Cloneopt Ab | Synthetically evolved DNA constructs for regulating signal peptide performance as well as vectors and host cells thereof |
SE544059C2 (en) * | 2020-02-07 | 2021-11-30 | Cloneopt Ab | Synthetically evolved dna constructs for regulating signal peptide performance as well as vectors and host cells thereof |
WO2021158163A1 (en) * | 2020-02-07 | 2021-08-12 | Xbrane Biopharma Ab | Synthetically evolved dna constructs for regulating signal peptide performance as well as vectors, host cells and recombinant proteins thereof |
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IL247632B (en) | 2021-02-28 |
AU2015229035A1 (en) | 2016-09-22 |
MA39746A (fr) | 2021-04-28 |
ES2897765T3 (es) | 2022-03-02 |
RU2748026C2 (ru) | 2021-05-19 |
US11390872B2 (en) | 2022-07-19 |
MX2021001460A (es) | 2021-04-28 |
JP6644717B2 (ja) | 2020-02-12 |
SI3116999T1 (sl) | 2021-12-31 |
EP3116999A1 (en) | 2017-01-18 |
RU2016140244A (ru) | 2018-04-17 |
JP2017510294A (ja) | 2017-04-13 |
WO2015139046A1 (en) | 2015-09-17 |
MX2016011637A (es) | 2017-04-13 |
KR102561695B1 (ko) | 2023-07-28 |
US20170029825A1 (en) | 2017-02-02 |
CN106103730A (zh) | 2016-11-09 |
CN106103730B (zh) | 2021-06-08 |
BR112016020822A2 (pt) | 2017-10-03 |
JP2020078305A (ja) | 2020-05-28 |
IL247632A0 (en) | 2016-11-30 |
US20200181625A1 (en) | 2020-06-11 |
KR20160134758A (ko) | 2016-11-23 |
CA2941687A1 (en) | 2015-09-17 |
PL3116999T3 (pl) | 2021-12-27 |
SG11201607519VA (en) | 2016-10-28 |
EP3116999B1 (en) | 2021-09-15 |
US10435694B2 (en) | 2019-10-08 |
AU2015229035B2 (en) | 2021-08-05 |
RU2016140244A3 (hr) | 2019-05-22 |
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