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希氏海萤荧光素酶:一种用于监测哺乳动物细胞基因表达的分泌型报告酶。

Vargula hilgendorfii luciferase: a secreted reporter enzyme for monitoring gene expression in mammalian cells.

作者信息

Thompson E M, Nagata S, Tsuji F I

机构信息

Osaka Bioscience Institute, Japan.

出版信息

Gene. 1990 Dec 15;96(2):257-62.

PMID:2269435
Abstract

The small marine ostracod crustacean, Vargula hilgendorfii, produces a bright blue luminous secretion which is ejected into seawater. The luminescence is due to a simple enzyme-catalyzed reaction involving only luciferase, luciferin (substrate), and molecular oxygen. Thus, V. hilgendorfii luciferase (VL) should be useful as a reporter enzyme in studies of gene expression in mammalian cells. Expression plasmids consisting of VL cDNA (vl) linked to the promoters simian virus 40 early region, Rous sarcoma virus long terminal repeat, human elongation factor, or mouse granulocyte colony-stimulating factor were introduced into a series of mammalian cell lines. Following transfection, VL activities in cell extracts and culture media were determined by a rapid light emission assay with V. hilgendorfii luciferin. Parallel experiments were carried out with the chloramphenicol acetyltransferase (CAT)-encoding gene. In all cell lines tested, VL was secreted, allowing the reporter activity to be determined directly from a small aliquot of the culture medium. The results indicate that the secreted VL enzyme is superior to CAT, firefly luciferase, and bacterial luciferase as a convenient and versatile indicator of gene expression in mammalian cells.

摘要

小型海洋介形甲壳动物希氏海萤(Vargula hilgendorfii)会产生一种亮蓝色的发光分泌物,并将其喷射到海水中。这种发光是由一个简单的酶催化反应引起的,该反应仅涉及荧光素酶、荧光素(底物)和分子氧。因此,希氏海萤荧光素酶(VL)在哺乳动物细胞基因表达研究中应可作为一种报告酶。将由与猿猴病毒40早期区域启动子、劳氏肉瘤病毒长末端重复序列、人延伸因子或小鼠粒细胞集落刺激因子相连的VL cDNA(vl)组成的表达质粒导入一系列哺乳动物细胞系。转染后,通过用希氏海萤荧光素进行的快速发光测定法来确定细胞提取物和培养基中的VL活性。用编码氯霉素乙酰转移酶(CAT)的基因进行了平行实验。在所有测试的细胞系中,VL都被分泌出来,从而可以直接从一小份培养基中测定报告活性。结果表明,作为哺乳动物细胞基因表达的一种方便且通用的指标,分泌型VL酶优于CAT、萤火虫荧光素酶和细菌荧光素酶。

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