Senapathy P, Jacob M T
J Biol Chem. 1981 Nov 25;256(22):11580-4.
Antibodies specific for the modified nucleoside N6-(delta 2-isopentenyl) adenosine (i6A) were employed to identify the tRNAs containing i6A from an unfractionated tRNA mixture by a nitrocellulose filter binding assay. When radioactive aminoacyl-tRNAs were incubated with i6A-specific antibodies and filtered through nitrocellulose membrane filters, the tRNAs possessing i6A (tRNAtyr and tRNAser) remained on the filters. tRNAarg and tRNAlys which do not contain i6A showed no binding. This finding will be useful as a very simple and rapid assay of such RNAs under a variety of conditions. Purification of i6A containing tRNAs from an unfractionated tRNA mixture was achieved by affinity chromatography of the tRNAs on an i6A antibody-Sepharose column. Nonspecific binding of tRNAs to the column was avoided by the use of purified antibodies.
针对修饰核苷N6-(δ2-异戊烯基)腺苷(i6A)的特异性抗体,通过硝酸纤维素滤膜结合试验,从未分级的tRNA混合物中鉴定出含有i6A的tRNA。当放射性氨酰-tRNA与i6A特异性抗体一起孵育并通过硝酸纤维素膜过滤时,含有i6A的tRNA(tRNAtyr和tRNAser)会留在滤膜上。不含i6A的tRNAarg和tRNAlys则没有结合。这一发现作为在各种条件下对这类RNA进行非常简单快速的检测方法将很有用。通过将tRNA在i6A抗体-琼脂糖柱上进行亲和层析,从未分级的tRNA混合物中纯化出含有i6A的tRNA。通过使用纯化抗体避免了tRNA与柱的非特异性结合。