DK2423315T3 - Fremgangsmåde til opnåelse af forbedret polypeptidekspression - Google Patents
Fremgangsmåde til opnåelse af forbedret polypeptidekspression Download PDFInfo
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Claims (16)
1. Fremgangsmåde til optimering af en nukleotidkodende sekvens, der koder for en forudbestemt aminosyresekvens, hvor den kodende sekvens optimeres til ekspression i en forudbestemt værtscelle, hvilken fremgangsmåde omfatter: a) frembringelse af mindst én oprindelig kodende sekvens, der koder for den forudbestemte aminosyresekvens; b) frembringelse af mindst én nydannet kodende sekvens fra den mindst ene oprindelige kodende sekvens ved substitution i den mindst ene oprindelige kodende sekvens af en eller flere kodoner med en synonym kodon; c) bestemmelse af en f itness-værdi for den mindst ene oprindelige kodende sekvens og en fitness-værdi for den mindst ene nydannede kodende sekvens ved anvendelse af en fitness-funktion, der bestemmer mindst én af enkeltkodon-fitness og kodonpar-fitness i forhold til den forudbestemte værtscelle; d) udvælgelse af en eller flere udvalgte kodende sekvenser blandt den mindst ene oprindelige kodende sekvens og den mindst ene nydannede kodende sekvens ifølge et forudbestemt udvælgelseskriterium, således at jo højere fitness-værdien er, jo højere er chancen for at blive udvalgt; e) gentagelse af trin b) til d) ved behandling af den ene eller de flere udvalgte kodende sekvenser som en eller flere oprindelige kodende sekvenser i trin b) til d) , indtil et forudbestemt gentagelses-stopkriterium er opfyldt; hvor fitness-funktionen defineres ved hjælp af:
hvor
cpi er en realværdi større end nul, fitcp(g) er en fitness-funktion for kodonpar, fitsc(g) er en fitness-funktion for en enkelt kodon, w((c(k), c(k + 1)) er vægten af et kodonpar i en kodende sekvens g, |g| er længden af den kodende sekvens, c(k) er den k-ende kodon i sekvensen af kodoner,
er en ønsket andel af kodon c(k), og
er en faktisk andel i den kodende sekvens g.
2. Fremgangsmåde ifølge krav 1, hvor det forudbestemte udvælgelseskriterium er således, at den ene eller de flere udvalgte kodende sekvenser har en bedste fitness-værdi ifølge et forudbestemt kriterium.
3. Fremgangsmåde ifølge krav 1 eller 2, hvor fremgangsmåden efter trin e) omfatter: f) udvælgelse af en bedste individuel kodende sekvens blandt den ene eller de flere udvalgte kodende sekvenser, hvor den bedste individuelle kodende sekvens har en bedre fitness-værdi end andre udvalgte kodende sekvenser.
4. Fremgangsmåde ifølge et hvilket som helst af kravene 1-3, hvor det forudbestemte gentagelses-stopkriterium er mindst én af: (a) test af om mindst én of de udvalgte kodende sekvenser har en bedste fitness-værdi over en forudbestemt tærskelværdi; (b) test af om ingen af de udvalgte kodende sekvenser har en bedste fitness-værdi under den forudbestemt tærskelværdi; (c) test af om mindst én af de udvalgte kodende sekvenser har mindst 30 % af kodonparrene med tilknyttede positive kodonparvægte for den forudbestemte værtscelle i den oprindelige kodende sekvens, der er transformeret til kodonpar med tilknyttede negative vægte; og (d) test af om mindst én af de udvalgte kodende sekvenser har mindst 30 % af kodonparrene med tilknyttede positive vægte over 0 for den forudbestemte værtscelle i den oprindelig kodende sekvens, der er transformeret til kodonpar med tilknyttede vægte under 0.
5. Fremgangsmåde ifølge et hvilket som helst af kravene 1-4, hvor cpi er mellem 10~4 og 0,5.
6. Fremgangsmåde ifølge et hvilket som helst af kravene 1-5, hvor kodonparvægtene w tages fra en 61 χ 61 kodonparmatrix uden stopkodoner eller en 61 χ 64 kodonparmatrix, der inkluderer stopkodoner, og hvor kodonparvægtene w beregnes på basis af en computerbaseret metode ved anvendelse som input af mindst én af: (a) en gruppe af nukleotidsekvenser, der består af mindst 200 kodende sekvenser fra en forudbestemt vært; (b) en gruppe af nukleotidsekvenser, der består af mindst 200 kodende sekvenser fra arten, som den forudbestemte vært tilhører; (c) en gruppe af nukleotidsekvenser, der består af mindst 5 % af de proteinkodende nukleotidsekvenser i en genomsekvens fra den forudbestemte vært; og (d) en gruppe af nukleotidsekvenser, der består af mindst 5 % af de proteinkodende nukleotidsekvenser i en genomsekvens fra en slægt, der er beslægtet med den forudbestemte vært.
7. Fremgangsmåde ifølge krav 6, hvor kodonparvægtene w bestemmes for mindst 5 %, 10 %, 20 %, 50 % og fortrinsvis 100 % af det mulige 61 χ 64 kodonpar, herunder termineringssignalet som stopkodon.
8. Fremgangsmåde ifølge krav 1-7, hvor kodonparvægtene w tages fra en 61 x 61 kodonparmatrix uden stopkodoner eller en 61 χ 64 kodonparmatrix, der inkluderer stopkodoner, og hvor kodonparvægtene w defineres ved hjælp af:
hvor de kombinerede forventede værdier
defineres ved hjælp af:
hvor
angiver enkeltkodonandelen af i datasættet for hele genomet og
forekomsten af et par (Ci,Cj) i den stærkt udtrykte gruppe, og hvor den stærkt udtrykte gruppe er generne, hvis mRNA'er kan detekteres ved et niveau på mindst 20 kopier pr. celle.
9. Fremgangsmåde ifølge et hvilket som helst af ovennævnte krav, hvor den oprindelige kodende nukleotidsekvens, der koder for en forudbestemt aminosyresekvens, er udvalgt blandt: (a) en vildtypenukleotidsekvens, der koder for den forudbestemte aminosyresekvens; (b) en revers translation af den forudbestemte aminosyresekvens, hvor en kodon for en aminosyreposition i den forudbestemte aminosyresekvens er vilkårligt udvalgt blandt de synonyme kodoner, der koder for aminosyren; og (c) en revers translation af den forudbestemte aminosyresekvens, hvor en kodon for en aminosyreposition i den forudbestemte aminosyresekvens er udvalgt i overenstemmelse med en enkeltkodontendens for den forudbestemte værtscelle eller en art, der er beslægtet med værtscellen.
10. Fremgangsmåde ifølge et hvilket som helst af kravene 1-9, hvor den forudbestemte værtscelle er en celle af en mikroorganisme, fortrinsvis en mikroorganisme fra en slægt, der er udvalgt blandt: Bacillus, Actinomycetis, Escherichia, Streptomyces, Aspergillus, Penicillium, Kluyveromyces, Saccharomyces.
11. Fremgangsmåde ifølge et hvilket som helst af kravene 1-9, hvor den forudbestemte værtscelle er en celle fra et dyr eller en plante, fortrinsvis en celle fra en cellelinje, der er udvalgt blandt CHO, BHK, NSO, COS, Vero, PER.C6™, HEK-293, Drosophila S2, Spodoptera Sf9 og Spodoptera Sf21.
12. Computer, der omfatter en processor og en hukommelse, hvilken processor er indrettet til at læse fra hukommelsen og skrive ind i hukommelsen, hvilken hukommelse omfatter data og instruktioner, der er beregnet til at få processoren til at udføre fremgangsmåden ifølge et hvilket som helst af kravene 1-11.
13. Computerprogramprodukt, der omfatter data og instruktioner og er beregnet til at blive indlæst i en hukommelse i en computer, der også omfatter en processor, hvilken processor er indrettet til at læse fra hukommelsen og skrive ind i hukommelsen, hvilke data og instruktioner er beregnet til at få processoren til at udføre fremgangsmåden ifølge et hvilket som helst af kravene 1-11.
14. Databærer, der er forsynet med et computerprogramprodukt ifølge krav 13.
15. Fremgangsmåde ifølge et hvilket som helst af kravene 1- 11, hvor den kodende sekvens, der koder for en forudbestemt aminosyresekvens, der er frembragt med fremgangsmåden, er indeholdt i et nukleinsyremolekyle, hvor den kodende sekvens ikke er en naturligt forekommende kodende sekvens, og hvor den kodende sekvens har en fitcp{g), der er mindst under -0,1, fortrinsvis under -0,2 og mere fortrinsvis under -0,3, for en forudbestemt værtscelle.
16. Fremgangsmåde ifølge et hvilket som helst af kravene 1- 11, hvor den kodende sekvens, der koder for en forudbestemt aminosyresekvens, der er frembragt med fremgangsmåden, er indeholdt i et nukleinsyremolekyle, hvor den kodende sekvens ikke er en naturligt forekommende kodende sekvens, og hvor den kodende sekvens har en fitcp{g), der er mindst under -0,1 og fortrinsvis under -0,2, for en forudbestemt værtscelle, og en fitSCi(g), der er mindst under 0,1, for en forudbestemt værtscelle.
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| EP06076328 | 2006-06-29 | ||
| EP07765439A EP2035561A1 (en) | 2006-06-29 | 2007-06-15 | A method for achieving improved polypeptide expression |
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| US (2) | US8812247B2 (da) |
| EP (2) | EP2423315B1 (da) |
| JP (1) | JP5250850B2 (da) |
| CN (1) | CN101490262B (da) |
| AU (1) | AU2007263880A1 (da) |
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| EA200900096A1 (ru) | 2009-06-30 |
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| BRPI0713795B1 (pt) | 2018-03-20 |
| CA2657975A1 (en) | 2008-01-03 |
| JP5250850B2 (ja) | 2013-07-31 |
| US20090286280A1 (en) | 2009-11-19 |
| ES2534282T3 (es) | 2015-04-21 |
| EP2423315B1 (en) | 2015-01-07 |
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