IP Library Granted Patent US 10,711,315
Granted Patent B2
US 10,711,315 · App. 16/005,131 · Granted Jul 14, 2020

Method for producing RNA

Inventors: Florian Von Der Mülbe (Stuttgart, DE); Ladislaus Reidel (Rottennburg am Neckar, DE); Thomas Ketterer (Gomaringen, DE); Lilia Gontcharova (Reutlingen, DE); Susanne Bauer (Bodelshausen, DE); Steve Pascolo (Zurich, CH); Jochen Probst (Wolfschlugen, DE); Andreas Schmid (Sigmaringen, DE)
Assignee: CureVac Real Estate GmbH
C12Q1/689C12N15/1003C12P19/34C12Q2600/158
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Quick Facts
Patent No.
US 10,711,315
App. No.
16/005,131
Granted
Jul 14, 2020
Kind
B2
Abstract

The present invention relates to a method for producing RNA. In particular, the present invention relates to a method for producing RNA, which is scalable and provides RNA at a high purity. The present invention provides a method for producing RNA under GMP and/or cGMP-compliant conditions. The invention further provides specific processes for use as a quality control in the manufacturing of a template DNA and/or in a method for producing RNA, in particular by in vitro transcription.

Claims (34)

1. A method for producing purified mRNA on a preparative scale comprising the following steps:

a) providing a template DNA comprising a nucleic acid sequence encoding a mRNA sequence;

b) in vitro transcription of the template DNA in order to obtain a composition comprising the mRNA;

c) purification of a preparative quantity of the mRNA obtained in step b) by purification steps comprising, at least:

i) oligo dT-based affinity purification; and

ii) RP-HPLC,

thereby producing a preparative quantity of purified mRNA.

2. The method of claim 1 , wherein the oligo dT-based affinity purification is performed before the RP-HPLC.

3. The method of claim 1 , wherein the RP-HPLC is performed before the oligo dT-based affinity purification.

4. The method of claim 1 , wherein the RP-HPLC is performed on a PLRP-S column.

5. The method of claim 1 , wherein the following steps are used to control the quality of the template DNA provided in step a):

I) determining the concentration of the template DNA in a sample;

II) determining the integrity of the template DNA;

III) determining the identity of the template DNA; and/or

IV) determining the purity of the template DNA.

6. The method of claim 1 , wherein the following steps are used to assess the quality of the mRNA obtained in steps b) or c):

i) determining the concentration of the mRNA or the purified mRNA in a sample;

ii) determining the integrity of the mRNA or the purified mRNA;

iii) determining the identity of the mRNA or the purified mRNA;

iv) determining the purity of the mRNA or the purified mRNA;

v) determining the pH of a sample comprising the mRNA or the purified mRNA;

vi) determining the osmolality of a sample comprising the mRNA or the purified mRNA;

vii) determining the presence and/or the amount of the template DNA in a sample comprising the mRNA or the purified mRNA; and/or

viii) determining the presence and/or the amount of an organic solvent in a sample comprising the mRNA or the purified mRNA.

7. The method of claim 1 , wherein the purified mRNA obtain in step c) comprises 1 to 5 grams of mRNA.

8. The method of claim 1 , wherein step a) comprises synthesis of the template DNA.

9. The method of claim 1 , wherein the template DNA is a DNA plasmid.

10. The method of claim 1 , wherein the in vitro transcription in step b) is carried out in presence of modified nucleotides.

11. The method of claim 1 , wherein the purification in step c) further comprises a precipitation step.

12. The method of claim 11 , wherein the precipitation step is an alcoholic precipitation step or a LiCl precipitation step.

13. The method of claim 1 , wherein the purification in step c) comprises a further chromatographic step selected from the group consisting of anion exchange chromatography, affinity chromatography, hydroxyapatite chromatography and core bead chromatography.

14. The method according to claim 11 , wherein the precipitation step if before the RP-HPLC.

15. The method according to claim 14 , wherein the precipitation step comprises LiCl precipitation.

16. The method according to claim 1 , wherein the mRNA obtained in step b) or the purified mRNA obtained in step c) is lyophilized.

Assignments (2)
CHANGE OF NAME Recorded Nov 12, 2022
From: CUREVAC REAL ESTATE GMBH
To: CUREVAC MANUFACTURING GMBH
Reel/Frame 061932/0502 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2020
From: CUREVAC AG
To: CUREVAC REAL ESTATE GMBH
Reel/Frame 051487/0680 →
Continuity (3)
Continuation 15044094 · Feb 15, 2016
Continuation PCTEP2015000959 · May 8, 2015
Related Publication 20180282790A1 · Oct 4, 2018
Cited By (15)
US 12,201,680 US 12,221,605 US 12,227,549 US 12,240,873 US 12,318,444 US 12,337,031 US 12,385,088 US 12,442,005 US 12,460,204 US 12,514,918 US 12,527,856 US 12,528,855 US 12,533,422 US 12,618,060 US 12,649,914