Schulte C, Schiltz E, Garrent R
Nucleic Acids Res. 1975 Jun;2(6):931-41. doi: 10.1093/nar/2.6.931.
After mild trypsin treatment of a complex of ribosomal protein S4 and 16S RNA of Escherichia coli, a large homogeneous fragment of the S4 protein was protected against digestion by its RNA binding site. This fragment was isolated and characterised for molecular weight. It was able to rebind specifically to 16S RNA. Preliminary results indicate that protected protein fragments can also be obtained from other proteins that complex specifically with 23S and 5S RNA.
用温和的胰蛋白酶处理大肠杆菌核糖体蛋白S4与16S RNA的复合物后,S4蛋白的一个大的均一性片段因其RNA结合位点而免受消化。分离出该片段并对其分子量进行了表征。它能够特异性地重新结合到16S RNA上。初步结果表明,受保护的蛋白片段也可以从与23S和5S RNA特异性结合的其他蛋白中获得。