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![Page 1: Promosome LLC, Scientific Presentation Scientific Presentation Expression Technologies for Enhancing Protein Production.](https://reader036.fdocuments.us/reader036/viewer/2022062408/56649f1c5503460f94c32dac/html5/thumbnails/1.jpg)
Promosome LLC, Scientific PresentationScientific Presentation
Expression Technologies for
Enhancing
Protein Production
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Promosome’s technologies enable increased protein production by increasing translation efficiencies
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1) initiation
2) elongation
3) termination
Background: Translation involves 3 stages
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Translation initiation involves ribosomal recruitment and recognition of a start site
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Ribosomal recruitment can occur at the m7G cap
via various eukaryotic initiation factors (eIFs)
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Ribosomal recruitment can also occur at an internal ribosome entry site (IRES)
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An initiation codon is then recognized and aribosomal complex forms at this site
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Translation Enhancer Elements (TEEs)
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Translational Enhancer Elements (TEEs)
TEEs are short nucleotide sequences that increase translation efficiency
Some function as ribosomal recruitment sites
Powerful synthetic translational enhancers have been generated by linking together five or more individual TEEs
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Gtx TEE can dramatically boost protein synthesisin some cell lines without increasing mRNA levels
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Activities of synthetic translational enhancers with 5 copies of individual TEEs in CHO-DG44 cells
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TEEs can enhance production of recombinant antibodies
Expression of this human antibody was enhanced maximally by TEEs in the 5’ leader of the L chain cistron
In this example, secretion of L chain dimers was also observed when L chain expression was enhanced
≈6-fold increase
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TEEs enhance expression of a hard-to-express mucin-Fc fusion protein
(Recopharma)
≈2-3-fold increase
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RESCUE
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RESCUE
Increases protein production by eliminating negative features in mRNAs that can decrease translation initiation
Primarily involves alterations in mRNA coding regions
- but does not involve altering codon utilization, minimizing potential alterations to protein secondary structure
Applicable to multiple cell types
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RESCUE examples in CHO cells
CAT enzyme (CHO-DG44) IgG L and H chain (CHO-K1)
EPO (CHO-DG44)
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RESCUE-modification of mucin-Fc fusion protein (Recopharma)
≈7-8 fold increase
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Summary
TEEsShort sequences identified for ability to enhance protein expression in CHO cells
Enable more protein to by synthesized per unit mRNA
May avoid limitations associated with high mRNA levels and enable high expressing cell lines without multiple chromosomal copies
RESCUEA novel technology is based on our new ideas about translation initiation
Potential advantages include increased protein expression and improved cell physiology
This technology appears to be broadly applicable to many cell types
RESCUE is expected to be compatible with other technologies