Gibson K J, Benkovic S J
Nucleic Acids Res. 1987 Aug 25;15(16):6455-67. doi: 10.1093/nar/15.16.6455.
To investigate protein-DNA interactions, we have synthesized a versatile phthalimide-protected 5-(3-aminopropyl)-2'-deoxyuridine nucleoside probe. The modified residue was incorporated into deoxyoligonucleotides by automated synthesis. The standard oligonucleotide workup also exposed the pendent amino group, which was found to react with either fluorescent labelling agents or, as detailed below, a photoactivatable cross-linking agent. In the dark, a strand with a photolabile group adjacent to the 3' end served as a primer for synthetic template-directed DNA synthesis by the Klenow fragment of E. coli DNA polymerase I, by bacteriophage T4 DNA polymerase, and by avian myeloblastosis virus (AMV) reverse transcriptase. Brief illumination with 302 nm light afforded covalent complexes between DNA and the polymerases; labelling of AMV reverse transcriptase was predominantly in the beta subunit.
为了研究蛋白质与DNA的相互作用,我们合成了一种通用的邻苯二甲酰亚胺保护的5-(3-氨丙基)-2'-脱氧尿苷核苷探针。通过自动合成将修饰的残基掺入脱氧寡核苷酸中。标准的寡核苷酸后处理也使侧链氨基暴露出来,发现该氨基可与荧光标记剂反应,或者如下所述,与光活化交联剂反应。在黑暗中,一条在3'端附近带有光不稳定基团的链作为引物,用于大肠杆菌DNA聚合酶I的Klenow片段、噬菌体T4 DNA聚合酶和禽成髓细胞瘤病毒(AMV)逆转录酶进行合成模板导向的DNA合成。用302 nm光短暂照射可使DNA与聚合酶之间形成共价复合物;AMV逆转录酶的标记主要在β亚基中。