Influence of different signal peptides and prosequences on expression and secretion of human tissue plasminogen activator in the baculovirus system
Foreign secretory pathway proteins are often produced in surprisingly low amounts in the baculovirus/insect cell expression system. One possible reason for this is that heterologous signal peptides might be inefficiently recognized by the insect cell protein translocation machinery. This idea was su...
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Veröffentlicht in: | The Journal of biological chemistry 1993-08, Vol.268 (22), p.16754-16762 |
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Zusammenfassung: | Foreign secretory pathway proteins are often produced in surprisingly low amounts in the baculovirus/insect cell expression
system. One possible reason for this is that heterologous signal peptides might be inefficiently recognized by the insect
cell protein translocation machinery. This idea was supported by a recent study showing that secretion of a plant protein
in the baculovirus system was enhanced when its signal peptide was replaced with an insect-derived signal peptide (Tessier,
D. C., Thomas, D. Y., Khouri, H. E., Laliberte, F., and Vernet, T. (1991) Gene (Amst.) 98, 177-183). We have extended these
observations by measuring the effects of different signal peptide and signal peptide-prosequence combinations on baculovirus-mediated
expression and secretion of human tissue plasminogen activator (t-PA). Replacement of the native prepropeptide with signal
peptides from a lepidopteran insect secretory protein (cecropin B), a major baculovirus structural glycoprotein (64K), or
an abundant, highly conserved lumenal protein of the rough endoplasmic reticulum (GRP78/BiP, a 78-kDa glucose-regulated protein/immunoglobulin
heavy chain-binding protein), had no significant effect on t-PA expression or secretion. The same results were obtained with
the signal peptide from honeybee prepromellitin, which was able to enhance secretion of plant propapain (Tessier et al., 1991
(above)). Similar results were obtained when heterologous signal peptides were combined with the native prosequence or when
the intact cecropin B preprosequence was used. Translational initiation at an upstream, in-frame ATT, which could functionally
inactivate any signal peptide, did not explain the low efficiency of t-PA secretion. Finally, deletion of the native signal
peptide, prosequence, or both, failed to increase t-PA production. These results showed that insect-derived signal peptides
and/or prosequences cannot always enhance the expression and/or secretion of foreign secretory pathway proteins in the baculovirus
system. They also suggested that the inability of insect cells to recognize the processing signals in human t-PA efficiently
is probably not the major factor preventing its high level production in this system. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/S0021-9258(19)85481-9 |