Methods for cell-free protein synthesis

1. A cell-free protein synthesis platform for preparing protein from a transcription template, the cell-free protein synthesis platform comprising a reaction mixture formed by combining:

(a) a Saccharomyces cerevisiae cellular extract prepared from mid-exponential to late-exponential cultures in the range from about 6 OD 600 to about 18 OD 600 ;

(b) a reaction buffer;

(c) a phage RNA polymerase; and

(d) the transcription template,

wherein the transcription template comprises: (i) at least one DNA encoding an open reading frame, (ii) a 5′-UTR comprising an internal ribosome entry site (IRES) or a cap-independent translation enhancer, and (iii) a 3′-UTR comprising a poly(A) 3′-terminus, and wherein the transcription template is operably linked to a promoter specific for the phage RNA polymerase; the phage RNA polymerase is capable of transcribing the transcription template to form a translation template; and the reaction mixture formed by combining (a), (b), (c), and (d) can sustain cell-free protein synthesis through a combined transcription/translation reaction.

2. The cell-free protein synthesis platform of claim 1 , wherein the Saccharomyces cerevisiae cellular extract comprises an S30 extract.

3. The cell-free protein synthesis platform of claim 1 , wherein the Saccharomyces cerevisiae cellular extract comprises an S60 extract.

4. The cell-free protein synthesis platform of claim 1 , wherein the reaction buffer comprises NTPs, spermidine, putrescine, a glutamate salt, a magnesium salt and glycerol.

5. The cell-free protein synthesis platform of claim 1 , wherein the reaction buffer comprises at least one component selected from the group consisting of NTPs, a polyamine, an organic anion, a divalent cation, an alcohol and combinations thereof.

6. The cell-free protein synthesis platform of claim 5 , wherein the polyamine is selected from spermidine and putrescine; the organic anion is selected from glutamate and acetate; the divalent cation is selected from magnesium, calcium and manganese; and the alcohol comprises glycerol.

7. The cell-free protein synthesis platform of claim 1 , wherein the Saccharomyces cerevisiae cellular extract is not pre-treated with a micrococcal nuclease.

8. The cell-free protein synthesis platform of claim 1 , wherein the phage RNA polymerase is selected from SP6 RNA Polymerase, T3 RNA Polymerase and T7 RNA polymerase.

9. The cell-free protein synthesis platform of claim 1 , wherein the phage RNA polymerase comprises T7 RNA polymerase.

10. The cell-free protein synthesis platform of claim 1 , wherein the at least one DNA comprises a linear DNA or a circular DNA.

11. The cell-free protein synthesis platform of claim 1 , wherein the at least one DNA comprises a linear DNA prepared from an amplification reaction.

12. The cell-free protein synthesis platform of claim 1 , wherein the 5′-UTR comprises a cap-independent translation enhancing element selected from the group consisting of a TMV Ω sequence, a TEV 5′-UTR element, and a Tbm 5′-UTR element.

13. The cell-free protein synthesis platform of claim 1 , wherein the 5′-UTR further comprises a yeast Kozak sequence or variant thereof.

14. The cell-free protein synthesis platform of claim 1 , wherein the poly(A) 3′-terminus ranges from about 20 nucleotides to about 200 nucleotides in length.

15. A method of performing high-throughput protein synthesis in vitro, comprising:

(a) providing a source nucleic acid;

(b) preparing a transcription template from the source nucleic acid; and

(c) synthesizing protein in vitro using a cell-free protein synthesis platform utilizing the transcription template, wherein the cell-free protein synthesis platform comprises a reaction mixture formed by combining:

(i) a Saccharomyces cerevisiae cellular extract prepared from mid-exponential to late-exponential cultures in the range from about 6 OD 600 to about 18 OD 600 ;

(ii) a reaction buffer;

(iii) a phage RNA polymerase, and

(iv) the transcription template,

wherein the transcription template comprises: (i) at least one DNA encoding an open reading frame, (ii) a 5′-UTR comprising an internal ribosome entry site (IRES) or a cap-independent translation enhancer, and (iii) a 3′-UTR comprising a poly(A) 3′-terminus, and wherein the transcription template is operably linked to a promoter specific for the phage RNA polymerase; the phage RNA polymerase is capable of transcribing from the transcription template to form the translation template, and the reaction mixture formed by combining (a), (b), (c), and (d) can sustain cell-free protein synthesis through a combined transcription/translation reaction.

16. The method of claim 15 , wherein the preparing a transcription template from the source nucleic acid comprises amplifying the source nucleic acid with a first primer and second primer in the presence of a DNA polymerase, wherein the first and second primers comprise gene-specific sequences capable of hybridizing the gene encoding an open reading frame in the source nucleic acid.

17. The method of claim 15 , wherein the transcription template comprises a linear DNA.

18. The method of claim 15 , wherein the phage RNA polymerase is selected from SP6 RNA Polymerase, T3 RNA Polymerase and T7 RNA polymerase.