IP Library Granted Patent US 12,595,501
Granted Patent B2
US 12,595,501 · App. 16/440,511 · Granted Apr 7, 2026

Expression of products from nucleic acid concatemers

Inventors: Brian Michael Davis (Niskayuna, NY); Erik Leeming Kvam (Niskayuna, NY); John Richard Nelson (Clifton Park, NY); Lisa Anne Lowery (Niskayuna, NY); Wei Gao (Clifton Park, NY)
Assignee: GLOBAL LIFE SCIENCES SOLUTIONS USA LLC
C12P21/02C12N7/00C12N15/1003C12N15/86C12P19/34C12N2015/8518C12N2750/14143
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,595,501
App. No.
16/440,511
Granted
Apr 7, 2026
Kind
B2
Abstract

Provided are techniques for generating expression products using one or more nucleic acid concatemers that include tandem repeats of a nucleic acid sequence encoding the expression product or products. In one embodiment, different expression products may be co-expressed using a concatemer mixture of a first nucleic acid concatemer and a second nucleic acid concatemer having a predefined ratio to one another.

Claims (42)

1 . A method comprising:

formulating a concatemer mixture comprising at least a first nucleic acid concatemer and a second nucleic acid concatemer having a predefined ratio to one another, wherein the first nucleic acid concatemer comprises tandem repeats of a first nucleic acid sequence and wherein the second nucleic acid concatemer comprises tandem repeats of a second nucleic acid sequence; and

co-expressing the concatemer mixture to generate a first expression product from the first nucleic acid sequence and a second expression product from the second nucleic acid sequence,

wherein the first nucleic acid concatemer, the second nucleic acid concatemer, or both are over 10 kb in length,

wherein the ratio of first expression product to the second expression product is proportional to the predefined ratio of the first nucleic acid concatemer to the second nucleic acid concatemer in the concatemer mixture, and

wherein the molar ratio of the first concatemer to the second concatemer is between 1:1 and 1:10.

2 . The method of claim 1 , comprising generating the first nucleic acid concatemer and the second nucleic acid concatemer using rolling circle amplification.

3 . The method of claim 2 , comprising using the rolling circle amplification to amplify circular or plasmid DNA to generate the first nucleic acid concatemer and/or the second nucleic acid concatemer.

4 . The method of claim 3 , wherein the first tandem repeats and/or the second tandem repeats are tandem repeats of the circular or plasmid DNA.

5 . The method of claim 1 , comprising transfecting cultured cells with the concatemer mixture to cause the co-expressing or wherein the co-expressing is in a cell-free expression system.

6 . The method of claim 1 , comprising collecting the first expression product and the second expression product.

7 . The method of claim 1 , wherein one or both of the first nucleic acid concatemer or the second nucleic acid concatemer is unprocessed before the co-expressing.

8 . The method of claim 1 , wherein the first expression product is an envelope or packing protein of a virus and the second expression product comprises a transgene of the virus, wherein the first expression product and the second expression product form a viral vector for delivering the transgene.

9 . The method of claim 1 , wherein the first expression product is a nucleic acid product and the second expression product is a protein product.

10 . The method of claim 9 , wherein the first expression product forms a complex with the second expression product.

11 . The method of claim 1 , wherein the first expression product acts on a third nucleic acid concatemer in the concatemer mixture.

12 . A method comprising:

formulating a mixture comprising at least a first nucleic acid concatemer, a second nucleic acid concatemer, and a third nucleic acid concatemer in a predefined ratio, wherein each of the nucleic acid concatemers comprises tandem repeats of two or more nucleic acid sequences; and

co-expressing the concatemer mixture to generate a first expression product, a second expression product, and a third expression product from each nucleic acid concatemer in the mixture,

wherein the first nucleic acid concatemer, the second nucleic acid concatemer, the third nucleic acid concatemer, or any combination thereof are over 10 kb in length,

wherein the molar ratio of the the first expression product, the second expression product, and the third expression product is proportional to the predefined molar ratio of the first nucleic acid concatemer, the second nucleic acid concatemer, and the third nucleic acid concatemer in the concatemer mixture, and

wherein the molar ratio of the first concatemer to the second concatemer to the third concatemer is C1:C2:C n , where C1, C2, and C n each is between 1 and 10.

13 . The method of claim 12 , wherein the nucleic acid sequence of an individual concatemer in the concatemer mixture comprises a plurality of expression sequences that, when expressed to generate the two or more expression products, generate a plurality of proteins.

14 . The method of claim 12 , wherein the nucleic acid sequence of an individual concatemer in the concatemer mixture comprises a plurality of expression sequences that, when expressed to generate the two or more expression products, generate a mix comprising at least one protein expression product and at least one nucleic acid expression product.

15 . A method, comprising:

amplifying at least one template comprising a first nucleic acid sequence using strand-displacement rolling circle amplification to a generate a first concatemer comprising tandem repeats of the first nucleic acid sequence;

contacting the first concatemer with a second concatemer comprising tandem repeats of a second nucleic acid sequence to form a concatemer mixture having a predefined ratio of the first nucleic acid concatemer to the second nucleic acid concatemer; and

co-expressing the concatemer mixture to generate a first expression product from the first nucleic acid sequence and a second expression product from the second nucleic acid sequence, wherein a ratio of the first expression product to the second expression product is proportional to the predefined ratio of the first nucleic acid concatemer to the second nucleic acid concatemer in the concatemer mixture,

wherein the molar ratio of the first concatemer to the second concatemer is between 1:1 and 1:10, and

wherein the first concatemer, the second concatemer, or both are over 10 kb in length.

16 . The method of claim 15 , comprising allowing the first expression product to form a complex with the second expression product.

17 . The method of claim 15 , wherein the first expression product and the second expression product comprise different viral products from a same virus.

18 . The method of claim 17 , wherein the same virus is an adenovirus or a lentivirus.

19 . The method of claim 15 , wherein the first expression product comprises a viral mRNA and the second expression product comprises a plurality of viral packaging proteins.

20 . A method comprising:

formulating a mixture comprising at least one nucleic acid concatemer and at least one plasmid having a predefined ratio to one another, wherein the at least one nucleic acid concatemer comprises tandem repeats of a first nucleic acid sequence and wherein the at least one plasmid comprises a second nucleic acid sequence; and

co-expressing the mixture to generate a first expression product from the first nucleic acid sequence and a second expression product from the second nucleic acid sequence,

wherein the molar ratio of the first concatemer to the plasmid is between 1:1 and 1:10,

wherein the first nucleic acid concatemer is over 10 kb in length, and

wherein the co-expression of the first expression product and the second expression product is ratiometric based on the predefined ratio.

21 . The method of claim 1 , wherein the co-expression of the first expression product and the second expression product is ratiometric based on the predefined ratio.

22 . The method of claim 12 , wherein the co-expression of the first expression product, the second expression product, and the third expression product is ratiometric based on the predefined ratio.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2020
From: GENERAL ELECTRIC COMPANY
To: GLOBAL LIFE SCIENCES SOLUTIONS USA LLC
Reel/Frame 053966/0133 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2019
From: DAVIS, BRIAN MICHAEL; KVAM, ERIK LEEMING; NELSON, JOHN RICHARD; LOWERY, LISA ANNE; GAO, WEI
To: GENERAL ELECTRIC COMPANY
Reel/Frame 049463/0675 →
Continuity (1)
Related Publication 20200392554A1 · Dec 17, 2020
References Cited (48)
US 5648245A · Fire et al. · 1997 [cited by applicant]
US 5807717A · Joyce · 1998 [cited by applicant]
US 6287824B1 · Lizardi · 2001 [cited by applicant]
US 6977153B2 · Kumar et al. · 2005 [cited by applicant]
US 7135312B2 · Kool · 2006 [cited by applicant]
US 7256020B2 · Lyamichev et al. · 2007 [cited by applicant]
US 7575865B2 · Leamon et al. · 2009 [cited by applicant]
US 7897380B2 · Kay et al. · 2011 [cited by applicant]
US 8715732B2 · Luo et al. · 2014 [cited by applicant]
US 8921072B2 · Nelson et al. · 2014 [cited by applicant]
US 9109250B2 · Hill · 2015 [cited by applicant]
US 9125845B2 · Nelson et al. · 2015 [cited by applicant]
US 9353393B2 · Nelson et al. · 2016 [cited by applicant]
US 20050079510A1 · Berka et al. · 2005 [cited by applicant]
US 20080153128A1 · Kim et al. · 2008 [cited by applicant]
US 20080160524A1 · Ma et al. · 2008 [cited by applicant]
US 20080220425A1 · Ma et al. · 2008 [cited by applicant]
US 20080305142A1 · Chen et al. · 2008 [cited by applicant]
US 20100008939A1 · Nelson et al. · 2010 [cited by applicant]
US 20170321239A1 · Nelson · 2017 [cited by examiner]
CN 106086012A · 2016 [cited by applicant]
EP 1489188A1 · 2004 [cited by applicant]
WO 2005003389A2 · 2005 [cited by applicant]
WO 200714608A1 · 2007 [cited by applicant]
WO 2014189768A1 · 2014 [cited by applicant]
WO 2016034849A1 · 2016 [cited by applicant]
WO 2017191007A1 · 2017 [cited by applicant]
WO 2018033730A1 · 2018 [cited by applicant]
WO 2019030155A1 · 2019 [cited by applicant]
WO 2019053039A1 · 2019 [cited by applicant]
WO 03072796A1 · 2023 [cited by applicant]
Celie Phn et al. Recombinant cloning strategies for protein expression. 2016. Current Opinion in Structural Biology. 38:145-154. (Year: 2016). [cited by examiner]
Grubaugh, Nathan D., et al.; “Mosquitoes Transmit Unique West Nile Virus Populations during Each Feeding Episode”, Cell Reports, vol. 19, Issue: 04, pp. 709-718, Apr. 25, 2017. [cited by applicant]
Weger-Lucarelli, James, et al.; “Rescue and Characterization of Recombinant Virus from a New World Zika Virus Infectious Clone”, Journal of Visualized Experiments, Issue: 124, pp. 01-08, Jun. 7, 2017. [cited by applicant]
Karbowniczek, Kinga, et al.; “Doggybone™ DNA: an advanced platform for AAV production”, Cell & gene therapy insights, pp. 731-738, Nov. 16, 2017. [cited by applicant]
Aliota, Matthew T., et al.; “Molecularly barcoded Zika virus libraries to probe in vivo evolutionary dynamics”, PLOS Pathogens, pp. 01-25, Mar. 28, 2018. [cited by applicant]
Weger-Lucarelli, James, et al.; “Using barcoded Zika virus to assess virus population structure in vitro and in Aedesaegypti mosquitoes”, Virology, vol. 521, pp. 138-148, Jun. 8, 2018. [cited by applicant]
PCT Search Report for PCT Application No. PC/EP2020/065980 mailed Aug. 3, 2020 (17 pages). [cited by applicant]
Japanese Office Action for JP Application No. 2018-557422 mailed Nov. 30, 2020 (12 pages with English translation). [cited by applicant]
Gagoski et al., “Gateway-Compatible Vectors for High-Throughput Protein Expression in Pro- and Eukaryotic Cell-Free Systems,” Journal of Biotechnology, 2015, 195:1-7. [cited by applicant]
Komar et al., “Synonymous Codon Substitutions Affect Ribosome Traffic and Protein Folding During in vitro Translation,” FEBS Letters 462, 1999, 387-393. [cited by applicant]
Sakatani et al., “A Transcription and Translation-Coupled DNA Replication System Using Rolling-Circle Replication,” Scientific Reports, 2015, 9 pages. [cited by applicant]
Kuhn et al., “Rolling-circle amplification under topological constraints”, Nucleic Acids Research, vol. 30, Issue 2, pp. 574-580, 2001. [cited by applicant]
Kumar et al., “Cell-free protein synthesis using multiply-primed rolling circle amplification products”, BioTeciniques, vol. 47, Issue 1, pp. 637-639, Jul. 2009. [cited by applicant]
Carlson et al., “Cell-free protein synthesis: Applications come of age”, Biotechnology Advances, 2011. [cited by applicant]
Kuhn et al., “Rolling-Circle Amplification of Duplex DNA Sequences assisted by PNA Openers,” pp. 227-243, https://www.bu.edu/cab/CAB PDF/Kuhn and Emidov DNA Amplification '04.pdf. [cited by applicant]
Japanese Office Action for JP Application No. 2021-573577, mailed Sep. 30, 2024 (13 pages with English translation). [cited by applicant]
Karda et al., “Production of lentiviral vectors using novel, enzymatically produced, linear DNA”, Gene Therapy, Jan. 2019, vol. 26, p. 86-92. [cited by applicant]