Jayabaskaran C
Biochem Int. 1984 Feb;8(2):257-64.
Antibodies specific for N6-(delta 2-isopentenyl) adenosine (i6A) were immobilized on Sepharose and this adsorbent (Sepharose-anti-i6A) was used to selectively isolate bacteriophage T4 tRNA precursors containing i6A/ms2i6A from an unfractionated population of 32P-labeled T4 RNAs. The results showed that antibodies to i6A selectively bound only those tRNA precursors containing i6A/ms2i6A. Binding of tRNA precursors by antibody and specificity of the binding was assessed by membrane binding using 32P-labeled tRNA precursor. Binding was highly specific for i6A/ms2i6A residues in the tRNA precursors. This binding can be used to separate modified from unmodified precursor RNAs and to study the biosynthetic pathways of tRNA precursors.
将对N6-(δ2-异戊烯基)腺苷(i6A)具有特异性的抗体固定在琼脂糖凝胶上,并用这种吸附剂(琼脂糖-抗-i6A)从32P标记的T4 RNA未分级群体中选择性分离含有i6A/ms2i6A的噬菌体T4 tRNA前体。结果表明,针对i6A的抗体仅选择性结合那些含有i6A/ms2i6A的tRNA前体。使用32P标记的tRNA前体通过膜结合评估抗体对tRNA前体的结合及结合特异性。该结合对tRNA前体中的i6A/ms2i6A残基具有高度特异性。这种结合可用于从未修饰的前体RNA中分离修饰的前体RNA,并研究tRNA前体的生物合成途径。