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不同信号肽和前导序列对杆状病毒系统中组织型纤溶酶原激活剂表达和分泌的影响

Influence of different signal peptides and prosequences on expression and secretion of human tissue plasminogen activator in the baculovirus system.

作者信息

Jarvis D L, Summers M D, Garcia A, Bohlmeyer D A

机构信息

Department of Entomology, Texas A&M University, College Station 77843.

出版信息

J Biol Chem. 1993 Aug 5;268(22):16754-62.

PMID:8344955
Abstract

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.

摘要

在杆状病毒/昆虫细胞表达系统中,外源分泌途径蛋白的产量常常低得出奇。一个可能的原因是,异源信号肽可能无法被昆虫细胞的蛋白质转运机制有效识别。最近的一项研究支持了这一观点,该研究表明,当植物蛋白的信号肽被昆虫来源的信号肽取代时,其在杆状病毒系统中的分泌会增强(Tessier, D. C., Thomas, D. Y., Khouri, H. E., Laliberte, F., and Vernet, T. (1991) Gene (Amst.) 98, 177 - 183)。我们通过测量不同信号肽和信号肽-前导序列组合对杆状病毒介导的人组织纤溶酶原激活物(t-PA)表达和分泌的影响,扩展了这些观察结果。用鳞翅目昆虫分泌蛋白(天蚕素B)、杆状病毒主要结构糖蛋白(64K)或粗糙内质网中一种丰富且高度保守的腔内蛋白(GRP78/BiP,一种78 kDa的葡萄糖调节蛋白/免疫球蛋白重链结合蛋白)的信号肽替换天然前原肽,对t-PA的表达或分泌没有显著影响。来自蜜蜂前催乳素原的信号肽也得到了相同的结果,该信号肽能够增强植物木瓜蛋白酶原的分泌(Tessier等人,1991年(见上文))。当异源信号肽与天然前导序列组合使用或使用完整的天蚕素B前原序列时,也得到了类似的结果。在一个上游的、符合读框的ATT处进行翻译起始,这可能会在功能上使任何信号肽失活,但并不能解释t-PA分泌效率低下的原因。最后,删除天然信号肽、前导序列或两者都删除,都未能增加t-PA的产量。这些结果表明,昆虫来源的信号肽和/或前导序列并不总能增强杆状病毒系统中外源分泌途径蛋白的表达和/或分泌。它们还表明,昆虫细胞无法有效识别人类t-PA中的加工信号,可能不是阻碍其在该系统中高水平产生的主要因素。

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