Rheinberger H J, Nierhaus K H
FEBS Lett. 1986 Aug 11;204(1):97-9. doi: 10.1016/0014-5793(86)81393-x.
A labeled tRNA present at the A, P or E site can be partially chased from the ribosome, a cognate nonlabeled tRNA as chasing substrate being 3-12-times more efficient than non-cognate tRNA at a molar ratio tRNA: 70 S = 10:1. These findings indicate that a tRNA bound to a programmed ribosome undergoes codon-anticodon interaction at all three sites (A, P and E site). Furthermore, both labeled tRNA present on the ribosome can be chased more effectively with cognate than with non-cognate substrate at the same time. This finding provides strong evidence that both tRNAs present on the ribosome exhibit simultaneous codon-anticodon interaction. This is valid for both the pretranslocational state (Ac[3H]Lys-tRNALys in the A and [14C]tRNALys in the P site) as well as the posttranslocational state (Ac[3H]Lys-tRNALys in the P and [14C]tRNALys in the E site).
位于A、P或E位点的标记tRNA可以从核糖体上被部分追踪,在tRNA与70S的摩尔比为10:1时,作为追踪底物的同源未标记tRNA比非同源tRNA的效率高3至12倍。这些发现表明,与编程核糖体结合的tRNA在所有三个位点(A、P和E位点)都发生密码子-反密码子相互作用。此外,核糖体上存在的两种标记tRNA同时被同源底物追踪的效果比非同源底物更好。这一发现提供了有力证据,证明核糖体上存在的两种tRNA都表现出同时的密码子-反密码子相互作用。这对于转位前状态(A位点的Ac[3H]Lys-tRNALys和P位点的[14C]tRNALys)以及转位后状态(P位点的Ac[3H]Lys-tRNALys和E位点的[14C]tRNALys)均成立。