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[α-(32)P]核苷三磷酸、环[32P]腺苷酸和环[32P]鸟苷酸的酶促制备。

The enzymatic preparation of [alpha-(32)P]nucleoside triphosphates, cyclic [32P] AMP, and cyclic [32P] GMP.

作者信息

Walseth T F, Johnson R A

出版信息

Biochim Biophys Acta. 1979 Mar 28;562(1):11-31. doi: 10.1016/0005-2787(79)90122-9.

Abstract

A method has been developed for the enzymatic preparation of alpha-(32)P-labeled ribo- and deoxyribonucleoside triphosphates, cyclic [(32)P]AMP, and cyclic [(32)P]GMP of high specific radioactivity and in high yield from (32)Pi. The method also enables the preparation of [gamma-(32)P]ATP, [gamma-(32)P]GTP, [gamma-(32)P]ITP, and [gamma-(32)P]-dATP of very high specific activity and in high yield. The preparation of the various [alpha-(32)P]nucleoside triphosphates relies on the phosphorylation of the respective 3'-nucleoside monophosphates with [gamma-(32)P]ATP by polynucleotide kinase and a subsequent nuclease reaction to form [5'-(32)P]nucleoside monophosphates. The [5'-(32)P]nucleoside monophosphates are then converted enzymatically to the respective triphosphates. All of the reactions leading to the formation of [alpha-(32)P]nucleoside triphosphates are carried out in the same reaction vessel, without intermediate purification steps, by the use of sequential reactions with the respective enzymes. Cyclic [(32)P]AMP and cyclic [(32)P]GMP are also prepared enzymatically from [alpha-(32)P]ATP or [alpha-(32)P]GTP by partially purified preparations of adenylate or guanylate cyclases. With the exception of the cyclases, all enzymes used are commerically available. The specific activity of (32)P-labeled ATP made by this method ranged from 200 to 1000 Ci/mmol for [alpha-(32)P]ATP and from 5800 to 6500 Ci/mmol for [gamma-(32)P]ATP. Minor modifications of the method should permit higher specific activities, especially for the [alpha-(32)P]nucleoside triphosphates. Methods for the use of the [alpha-(32)P]nucleoside phosphates are described for the study of adenylate and guanylate cyclases, cyclic AMP- and cyclic GMP phosphodiesterase, cyclic nucleotide binding proteins, and as precursors for the synthesis of other (32)P-labeled compounds of biological interest. Moreover, the [alpha-(32)P]nucleoside triphosphates prepared by this method should be very useful in studies on nucleic acid structure and metabolism and the [gamma-(32)P]nucleoside triphosphates should be useful in the study of phosphate transfer systems.

摘要

已开发出一种方法,可通过酶促反应从³²Pi高效制备高比放射性的α-(³²P)标记的核糖核苷三磷酸和脱氧核糖核苷三磷酸、环[(³²P) ]AMP及环[(³²P) ]GMP。该方法还能高效制备比活性极高的[γ-(³²P)]ATP、[γ-(³²P)]GTP、[γ-(³²P)]ITP及[γ-(³²P)]-dATP。各种α-(³²P)核苷三磷酸的制备依赖于用多核苷酸激酶使相应的3'-核苷单磷酸与[γ-(³²P)]ATP磷酸化,随后进行核酸酶反应以形成[5'-(³²P)]核苷单磷酸。然后将[5'-(³²P)]核苷单磷酸酶促转化为相应的三磷酸。导致形成α-(³²P)核苷三磷酸的所有反应均在同一反应容器中进行,无需中间纯化步骤,通过与相应酶的顺序反应来实现。环[(³²P) ]AMP和环[(³²P) ]GMP也通过部分纯化的腺苷酸环化酶或鸟苷酸环化酶制剂由α-(³²P)ATP或α-(³²P)GTP酶促制备。除环化酶外,所用的所有酶均有商业供应。用该方法制备的³²P标记的ATP的比活性,α-(³²P)ATP为200至1000 Ci/mmol,γ-(³²P)ATP为5800至6500 Ci/mmol。对该方法稍作修改应可获得更高的比活性,尤其是对于α-(³²P)核苷三磷酸。文中描述了使用α-(³²P)核苷磷酸来研究腺苷酸环化酶和鸟苷酸环化酶、环AMP和环GMP磷酸二酯酶、环核苷酸结合蛋白,以及作为合成其他具有生物学意义的³²P标记化合物的前体的方法。此外,用该方法制备的α-(³²P)核苷三磷酸在核酸结构和代谢研究中应非常有用,而γ-(³²P)核苷三磷酸在磷酸转移系统研究中应很有用。

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