Early post-transfection isolation of cells (epic) for biologics production
Abstract
Provided herein are methods for selecting a population of cells expressing a target polypeptide. In some aspects, the disclosure provides methods for sorting and selecting populations of transfected host cells based on their early expression of a selectable polypeptide. In certain embodiments, the sorting is performed using fluorescence-activated cell sorting or magnetic-activated cell sorting based on the selectable polypeptide. Such selection methods can be further utilized to generate clonal populations of producer cells, e.g. for large-scale manufacturing of a target polypeptide of interest.
Claims
exact text as granted — not AI-modified1 - 30 . (canceled)
31 . A method of producing a population of producer cells expressing a target polypeptide, the method comprising:
(a) transfecting host cells with one or more vectors that encode one or more mRNAs, wherein the one or more mRNAs encode a selectable polypeptide and the target polypeptide; (b) isolating from the transfected host cells, within 2 to 15 days of transfection, a sub-population of early-expressing transfected host cells which express the selectable polypeptide; and (c) expanding the sub-population of transfected host cells, thereby producing a population of producer cells expressing the target polypeptide.
32 . The method of claim 31 , wherein steps (b) and (c) are each performed in drug-selection-free medium.
33 . The method of claim 31 , further comprising isolating the target polypeptide from the population of producer cells.
34 . The method of claim 31 , further comprising isolating one or more single transfected host cells from the expanded sub-population and culturing the one or more single transfected host cells to produce clonal populations of the one or more single transfected host cells.
35 . The method of claim 34 , wherein at least one of the clonal populations of the one or more single transfected host cells yields a 2- to 30-fold improvement in production of the target polypeptide compared to that of a stable pool of transfected but uncloned host cells obtained at step (c).
36 . The method of claim 31 , wherein the transfected host cells subject to selection in (b) contains at least 80-120×10 6 cells.
37 . The method of claim 31 , wherein the isolating in step (b) is performed less than 6 days after transfection.
38 . The method of claim 31 , wherein the sub-population of transfected host cells contains 0.5-6.0×10 6 cells prior to expansion in step (c).
39 . The method of claim 31 , wherein the expanding in step (c) is for between 4-31 days.
40 . The method of claim 31 , wherein a first of the one or more vectors encodes the mRNA encoding the target polypeptide and a second of the one or more vectors encodes the mRNA encoding the selectable polypeptide.
41 . The method of claim 31 , wherein the mRNA encoding the target polypeptide and the mRNA encoding the selectable polypeptide are both encoded on one vector.
42 . The method of claim 31 , wherein the target polypeptide and the selectable polypeptide form a fusion polypeptide.
43 . The method of claim 31 , wherein the target polypeptide and the selectable polypeptide are encoded by a single multicistronic mRNA.
44 . The method of claim 43 , wherein the multicistronic mRNA comprises a first open reading frame (ORF) that encodes the selectable polypeptide and a second ORF that encodes the target polypeptide, wherein the first ORF is 5′ to the second ORF.
45 . The method of claim 44 , wherein the first ORF has a non-AUG start codon.
46 . The method of claim 44 , wherein the second ORF has an AUG start codon.
47 . The method of claim 44 , wherein the ORF that encodes the selectable polypeptide is devoid of any AUG sequences.
48 . The method of claim 31 , wherein the selectable polypeptide is CD52 or CD59.
49 . A clonal population of transfected host cells that express a selectable polypeptide and a target polypeptide obtainable by the method of claim 31 .
50 . The clonal population of claim 49 , wherein the clonal population yields a 2- to 30-fold improvement in production of the target polypeptide compared to that of the sub-population of transfected host cells in (b).Join the waitlist — get patent alerts
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