Shaw J E, Huang E S, Pagano J S
J Virol. 1975 Jul;16(1):132-40. doi: 10.1128/JVI.16.1.132-140.1975.
A simple method is described for the iodination of herpes simplex virus (HSV) DNA. The procedure involved synthesis of 125-I-labeled 5-iodo-dCTP which was subsequently used as a precursor for the in vitro repair synthesis of HSV DNA. Synthesis of 5-iodo-dCTP and purification from oxidation and reduction reagents, buffer salts, unreacted dCTP and Na125-I was accomplished in a single chromatographic step. It was possible to prepare 125-I-labeled HSV DNA in vitro with specific activities exceeding 10-8 counts/min/mu-g. The DNA prepared by this method reassociated with DNA extracted from HSV-infected HEp-2 cells but not with HEp-2 cell DNA. Iodinated HSV DNA was susceptible to S-1-endonuclease digestion once denatured but was resistant to digestion in the native form. This method was used to synthesize 125-I-labeled ribo-CTP (5-iodo-CTP) which was used to prepare cytomegalovirus-specific complementary RNA. The method should be of value in the preparation of viral probes and for use in autoradiography of viral nucleic acids.
描述了一种用于单纯疱疹病毒(HSV)DNA碘化的简单方法。该过程包括合成125I标记的5-碘-dCTP,随后将其用作HSV DNA体外修复合成的前体。5-碘-dCTP的合成以及从氧化还原试剂、缓冲盐、未反应的dCTP和Na125-I中纯化,通过单一色谱步骤即可完成。有可能在体外制备比活性超过10-8计数/分钟/微克的125I标记的HSV DNA。通过该方法制备的DNA与从HSV感染的HEp-2细胞中提取的DNA重新结合,但不与HEp-2细胞DNA结合。碘化的HSV DNA一旦变性就易受S-1核酸内切酶消化,但天然形式下对消化具有抗性。该方法用于合成125I标记的核糖-CTP(5-碘-CTP),用于制备巨细胞病毒特异性互补RNA。该方法在制备病毒探针以及用于病毒核酸的放射自显影方面应具有价值。