Muralikrishna P, Alexander R W, Cooperman B S
Department of Chemistry, University of Pennsylvania, Philadelphia, PA 19104-6323, USA.
Nucleic Acids Res. 1997 Nov 15;25(22):4562-9. doi: 10.1093/nar/25.22.4562.
We report the synthesis of a radioactive, photolabile oligodeoxyribonucleotide probe and its exploitation in identifying 50S ribosomal subunit components neighboring the alpha-sarcin loop. The probe is complementary to 23S rRNA nt 2653-2674. Photolysis of the complex formed between the probe and 50S subunits leads to site-specific probe photoincorporation into proteins L2, the most highly labeled protein, L1, L15, L16 and L27, labeled to intermediate extents, and L5, L9, L17 and L24, each labeled to a minor extent. Portions of each of these proteins thus lie within 23 A of nt U2653. These results lead us to conclude that the alpha-sarcin loop is located at the base of the L1 projection within the 50S subunit. Such placement, near the peptidyl transferase center, provides a rationale for the extreme sensitivity of ribosomal function to cleavage of the alpha-sarcin loop.
我们报道了一种放射性、光不稳定的寡脱氧核糖核苷酸探针的合成及其在鉴定与α-肌动蛋白环相邻的50S核糖体亚基成分中的应用。该探针与23S rRNA的第2653 - 2674核苷酸互补。探针与50S亚基形成的复合物经光解后,会导致探针在特定位置光掺入蛋白质L2(标记程度最高)、L1、L15、L16和L27(标记程度中等)以及L5、L9、L17和L24(标记程度较低)。因此,这些蛋白质中的每一种的部分区域位于核苷酸U2653的23埃范围内。这些结果使我们得出结论,α-肌动蛋白环位于50S亚基中L1突起的基部。这种位于肽基转移酶中心附近的位置,为核糖体功能对α-肌动蛋白环切割的极端敏感性提供了一个解释。