IP Library Granted Patent US 8,999,380
Granted Patent B2
US 8,999,380 · App. 13/791,922 · Granted Apr 7, 2015

Modified polynucleotides for the production of biologics and proteins associated with human disease

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Quick Facts
Patent No.
US 8,999,380
App. No.
13/791,922
Granted
Apr 7, 2015
Kind
B2
Abstract

The invention relates to compositions and methods for the preparation, manufacture and therapeutic use of polynucleotides, primary transcripts and mmRNA molecules.

Claims (20)

1. An isolated polynucleotide comprising;

(a) a first region of linked nucleosides, said first region encoding a polypeptide of interest, said polypeptide of interest is SEQ ID NO: 1089;

(b) a first flanking region located at the 5′ terminus of said first region comprising at least one 5′ terminal cap;

(c) a second flanking region located at the 3′ terminus of said first region comprising a 3′ tailing sequence of linked nucleosides; and

wherein at least one of said linked nucleosides of (a) comprises at least one modification as compared to the chemical structure of an A, G, U or C ribonucleoside.

2. The isolated polynucleotide of claim 1 , wherein the 3′ tailing sequence of linked nucleosides is selected from the group consisting of a poly-A tail of approximately 160 nucleotides and a polyA-G quartet.

3. The isolated polynucleotide of any one of claim 1 or 2 which is purified.

4. The isolated polynucleotide of claim 1 or 2 , wherein the at least one 5′ terminal cap is selected from the group consisting of Cap0, Cap 1, ARCA, inosine, N1-methyl-guanosine, 2′fluoro-guanosine, 7-deaza-guanosine, 8-oxo-guanosine, 2-amino-guanosine, LNA-guanosine and 2-azido-guanosine.

5. The isolated polynucleotide of claim 1 , wherein the at least one modification does not form the nucleoside pseudouridine (ψ) or 5-methyl-cytidine (m 5 C).

6. The isolated polynucleotide of anyone of claim 1 or 2 , further comprising a targeting moiety, wherein said targeting moiety is covalently bound to said isolated polynucleotide.

7. The isolated polynucleotide of claim 6 , wherein said targeting moiety is an antibody, thyrotropin, melanotropin, lectin, glycoprotein, surfactant protein A, Mucin carbohydrate, multivalent lactose, multivalent galactose, N-acetyl-galactosamine, N-acetyl-gulucosamine multivalent mannose, multivalent fucose, glycosylated polyaminoacids, multivalent galactose, transferrin, bisphosphonate, polyglutamate, polyaspartate, a lipid, cholesterol, a steroid, bile acid, folate, vitamin B12, biotin, an RGD peptide, an RGD peptide mimetic, or an aptamer.

8. The isolated polynucleotide of claim 1 , wherein the first region is codon optimized.

9. The isolated polynucleotide of claim 1 , wherein the first flanking region comprises a 5′ untranslated region and the second flanking region comprises a 3′ untranslated region.

10. The isolated polynucleotide of claim 9 , wherein at least one of the 5′ untranslated region of the 3′ untranslated region is not derived from the native untranslated region of the polypeptide of interest.

11. The isolated polynucleotide of claim 9 , wherein the 5′ untranslated region and the 3′ untranslated region are not derived from the same species.

12. The isolated polynucleotide of claim 9 , wherein at least one of the 5′ untranslated region or the 3′ untranslated region is not derived from beta-globin.

13. The isolated polynucleotide of claim 1 , wherein the at least one modification forms the nucleoside N1-methylpseudouridine.

14. The isolated polynucleotide of claim 13 , wherein said isolated polynucleotide further comprises at least one modification to form the nucleoside 5-methyl-cytidine.

15. The isolated polynucleotide of claim 1 , wherein said isolated polynucleotide comprises two modifications and wherein the first modification forms the nucleoside 2-thiouridine and the second modification forms the nucleoside 5-methyl-cytosine.

16. The isolated polynucleotide of claim 15 , wherein 25% of the cytosine residues are 5-methyl-cytosine and 25% of the uridine residues are 2-thiouridine.

Assignments (10)
SECURITY INTEREST Recorded Nov 19, 2025
From: MODERNATX, INC.
To: ARES CAPITAL CORPORATION, AS AGENT
Reel/Frame 073634/0354 →
CHANGE OF NAME Recorded Mar 28, 2018
From: MODERNA THERAPEUTICS, INC.
To: MODERNATX, INC.
Reel/Frame 045755/0844 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY'S NAME PREVIOUSLY RECORDED AT REEL: 030026 FRAME: 0313. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 19, 2014
From: SCHRUM, JASON P.
To: MODERNA THERAPEUTICS, INC.
Reel/Frame 034678/0847 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY NAME AND ADDRESS PREVIOUSLY RECORDED AT REEL: 030041 FRAME: 0388. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 19, 2014
From: CHAKRABORTY, TIRTHA; DE FOUGEROLLES, ANTONIN; ELBASHIR, SAYDA E.; JOHN, MATTHIAS; ROY, ATANU; WHORISKEY, SUSAN; WOOD, KRISTY M.; ELLSWORTH, JEFF LYNN; GUILD, JUSTIN; HATALA, PAUL
To: MODERNA THERAPEUTICS, INC.
Reel/Frame 034839/0703 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY NAME PREVIOUSLY RECORDED AT REEL: 030187 FRAME: 0748. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 18, 2014
From: BANCEL, STEPHANE
To: MODERNA THERAPEUTICS, INC.
Reel/Frame 034679/0346 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2014
From: EJEBE, KENECHI, DR.
To: MODERNA THERAPEUTICS, INC.
Reel/Frame 033848/0044 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2013
From: BANCEL, STEPHANE
To: MODERNA THERAPEUTICS
Reel/Frame 030187/0748 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2013
From: CHAKRABORTY, TIRTHA; DE FOUGEROLLES, ANTONIN; ELBASHIR, SAYDA M.; JOHN, MATTHIAS; ROY, ATANU; WHORISKEY, SUSAN; WOOD, KRISTY M.; ELLSWORTH, JEFF LYNN; GUILD, JUSTIN; HATALA, PAUL
To: MODERNA THERAPEUTICS
Reel/Frame 030041/0388 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 18, 2013
From: SCHRUM, JASON P.
To: MODERNA THERAPEUTICS
Reel/Frame 030026/0313 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 18, 2013
From: EJEBE, KENECHI G.
To: MODERNA THERAPEUTICS
Reel/Frame 030026/0570 →