Osswald M, Döring T, Brimacombe R
Max-Planck-Institut fuer Molekulare Genetik (AG Ribosomen), Berlin (Dahlem), Germany.
Nucleic Acids Res. 1995 Nov 25;23(22):4635-41. doi: 10.1093/nar/23.22.4635.
The naturally occurring nucleotide 3-(3-amino-3-carboxy-propyl)uridine (acp3U) at position 47 of tRNA(Phe) from Escherichia coli was modified with a diazirine derivative and bound to ribosomes in the presence of suitable mRNA analogues under conditions specific for the ribosomal A, P or E sites. After photo-activation at 350 nm the cross-links to ribosomal proteins and RNA were identified by our standard procedures. In the 30S subunit protein S19 (and weakly S9 and S13) was the target of cross-linking from tRNA at the A site, S7, S9 and S13 from the P site and S7 from the E site. Similarly, in the 50S subunit L16 and L27 were cross-linked from the A site, L1, L5, L16, L27 and L33 from the P site and L1 and L33 from the E site. Corresponding cross-links to rRNA were localized by RNase H digestion to the following areas: in 16S rRNA between positions 687 and 727 from the P and E sites, positions 1318 and 1350 (P site) and 1350 and 1387 (E site); in the 23S rRNA between positions 865 and 910 from the A site, 1845 and 1892 (P site), 1892 and 1945 (A site), 2282 and 2358 (P site), 2242 and 2461 (P and E sites), 2461 and 2488 (A site), 2488 and 2539 (all three sites) and 2572 and 2603 (A and P sites). In most (but not all) cases, more precise localizations of the cross-link sites could be made by primer extension analysis.
来自大肠杆菌的tRNA(Phe)第47位的天然存在的核苷酸3-(3-氨基-3-羧基丙基)尿苷(acp3U)用二氮杂环丙烷衍生物进行修饰,并在适合核糖体A、P或E位点的条件下,于合适的mRNA类似物存在时与核糖体结合。在350nm处进行光活化后,通过我们的标准程序鉴定与核糖体蛋白质和RNA的交联。在30S亚基中,蛋白质S19(以及较弱的S9和S13)是A位点tRNA交联的靶标,P位点的S7、S9和S13以及E位点的S7是靶标。同样,在50S亚基中,L16和L27是A位点交联的靶标,P位点的L1、L5、L16、L27和L33以及E位点的L1和L33是靶标。通过RNase H消化将与rRNA的相应交联定位到以下区域:在16S rRNA中,P和E位点的687至727位之间、1318和1350位(P位点)以及1350和1387位(E位点);在23S rRNA中,A位点的865至910位之间、1845和1892位(P位点)、1892和1945位(A位点)、2282和2358位(P位点)、2242和2461位(P和E位点)、2461和2488位(A位点)、2488和2539位(所有三个位点)以及2572和2603位(A和P位点)。在大多数(但不是全部)情况下,通过引物延伸分析可以对交联位点进行更精确的定位。