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Analysis of an insect neuropeptide, Schistocerca gregaria ion transport peptide (ITP), expressed in insect cell systems

机译:分析在昆虫细胞系统中表达的昆虫神经肽血吸虫血红蛋白离子转运肽(ITP)

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An active form of Schistocerca gregaria ion transport peptide (ITP) in an insect cell expression system was produced. Transformed Drosophila Kc1 cells secreted a form of ITP into the cell culture medium that was proteolytically cleaved correctly atthe amino (N)-terminus. Concentrated culture supernatant from transformed Kc1 and Hi5 cells had high biological activity when tested on isolated locust ilea. Conversely, ITP expressed by baculovirus-infected Sf9 cells was larger in size and had decreasedspecific activity compared to ITP produced by Kc1 cells due to incorrect cleavage of the peptide at the N-terminus in the baculovirus system. This demonstrates how processing of the secreted foreign protein (ITP) expressed under the late polyhedrin promoter is compromised in a baculovirus-infected cell. Transient transformation of Kc1 cells results in supernatants containing two forms of ITP; one form (A) co-elutes with synthetic ITP and the other form (B) has reduced electrophoretic mobility. In contrast, in stably transformed Kc1 cell supernatant, ITP is expressed in a single form, which has the same electrophoretic mobility and specific biological activity as form A produced by transiently transformed Kc1 cells.
机译:在昆虫细胞表达系统中产生了一种活性形式的血吸虫裂殖子离子转运肽(ITP)。转化的果蝇Kc1细胞将一种ITP形式分泌到细胞培养基中,该蛋白质在氨基(N)端被蛋白水解正确地裂解。当在分离的刺槐回肠上进行测试时,来自转化的Kc1和Hi5细胞的浓缩培养物上清液具有较高的生物活性。相反,由于杆状病毒系统中N末端肽的错误切割,与杆状病毒感染的Sf9细胞表达的ITP相比,由Kc1细胞产生的ITP尺寸更大,比活性降低。这证明了在杆状病毒感染的细胞中如何破坏在多角体蛋白晚期启动子下表达的分泌外源蛋白(ITP)的加工。 Kc1细胞的瞬时转化导致上清液中包含两种形式的ITP。一种形式(A)与合成ITP共洗脱,另一种形式(B)具有降低的电泳迁移率。相反,在稳定转化的Kc1细胞上清液中,ITP以单一形式表达,其电泳迁移率和比生物学活性与瞬时转化的Kc1细胞产生的A型相同。

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