This work was funded by Human Frontier Science Program grant RGP0024.

1. DNA Template Preparation and in vitro Transcription
<ol>
 <li>The gene of interest is cloned under T7 and/or e.g. SP6 transcriptional promoter.</li>
 <li>For in vitro transcription the template DNA is linearized with an appropriate restriction enzyme cutting downstream of the ORF stop codon and/or mRNA 3' end. One needs to verify complete linearization of the plasmid DNA by running the restriction digestion product on agarose gel electrophoresis.</li>
 <li>The linearized plasmid is used for in ...

<ol>
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For reproducible results, quality and concentration of the components used for in vitro transcription and translation reactions are critical. In the current study we have used commercially available kits and extracts that provide highly reproducible data, if handled carefully. However, translation-competent extracts can be prepared from the cell of one's choice, if needed. Quality of mRNA can affect the translation, so it is of utmost importance to test the integrity of mRNAs before using it during in vitro<...

<table border="1">
	<tbody>
		<tr>
			<td>Name of reagent/ Kit</td>
			<td>Company</td>
			<td>Catalogue number</td>
		</tr>
		<tr>
			<td>MEGAscript T7 High yield Transcription Kit</td>
			<td>Ambion</td>
			<td>AM1333</td>
		</tr>
		<tr>
			<td>Ribonuclease Inhibitor</td>
			<td>Invitrogen</td>
			<td>15518012</td>
		</tr>
		<tr>
			<td>Trans [35S]-Label</td>
			<td>MP Biomedicals</td>
			<td>0151006</td>
		</tr>
		<tr>
			<td>Ribonuclease-A</td>
			<td>Invitrogen</td>
			<td>12091</td>
		</tr>
		<tr>
			<td>Rabbit Reticulocyte Lysate System, Nuclease Treated</td>
			<td>Promega</td>
			<td>L4960</td>
		</tr>
		<tr>
			<td>E. coli S30 Extract System for Linear Templates</td>
			<td>Promega</td>
			<td>L1030</td>
		</tr>
		<tr>
			<td>Centrifugation</td>
			<td>Beckman Coulter</td>
			<td>Optima TLX Ultracentrifuge</td>
		</tr>
		<tr>
			<td>Storage phosphor autoradiography</td>
			<td>GE Healthcare</td>
			<td>Typhoon 9410 variable mode imager</td>
		</tr>
		<tr>
			<td>Software for nascent polypeptide analysis</td>
			<td>GE Healthcare</td>
			<td>Image Quant TL, v2005</td>
		</tr>
	</tbody>
</table>

isolation of ribosome bound nascent polypeptides in vitro to identify translational pause sites along mrna

The rate of translational elongation is non-uniform. mRNA secondary structure, codon usage and mRNA associated proteins may alter ribosome movement on the messagefor review see 1. However, it's now widely accepted that synonymous codon usage is the primary cause of non-uniform translational elongation rates1. Synonymous codons are not used with identical frequency. A bias exists in the use of synonymous codons with some codons used more frequently than others2. Codon bias is organism as well as tissue specific2,3. Moreover, frequency of codon usage is directly proportional to the concentrations of cognate tRNAs4. Thus, a frequently used codon will have higher multitude of corresponding tRNAs, which further implies that a frequent codon will be translated faster than an infrequent one. Thus, regions on mRNA enriched in rare codons (potential pause sites) will as a rule slow down ribosome movement on the message and cause accumulation of nascent peptides of the respective sizes5-8. These pause sites can have functional impact on the protein expression, mRNA stability and protein foldingfor review see 9. Indeed, it was shown that alleviation of such pause sites can alter ribosome movement on mRNA and subsequently may affect the efficiency of co-translational (in vivo) protein folding1,7,10,11. To understand the process of protein folding in vivo, in the cell, that is ultimately coupled to the process of protein synthesis it is essential to gain comprehensive insights into the impact of codon usage/tRNA content on the movement of ribosomes along mRNA during translational elongation.
Here we describe a simple technique that can be used to locate major translation pause sites for a given mRNA translated in various cell-free systems6-8. This procedure is based on isolation of nascent polypeptides accumulating on ribosomes during in vitro translation of a target mRNA. The rationale is that at low-frequency codons, the increase in the residence time of the ribosomes results in increased amounts of nascent peptides of the corresponding sizes. In vitro transcribed mRNA is used for in vitro translational reactions in the presence of radioactively labeled amino acids to allow the detection of the nascent chains. In order to isolate ribosome bound nascent polypeptide complexes the translation reaction is layered on top of 30% glycerol solution followed by centrifugation. Nascent polypeptides in polysomal pellet are further treated with ribonuclease A and resolved by SDS PAGE. This technique can be potentially used for any protein and allows analysis of ribosome movement along mRNA and the detection of the major pause sites. Additionally, this protocol can be adapted to study factors and conditions that can alter ribosome movement and thus potentially can also alter the function/conformation of the protein.

Watch this Scientific Journal Video about Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA at JoVE.com

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA

A technique to identify translational pause sites on mRNA is described. This procedure is based on isolation of nascent polypeptides accumulating on ribosomes during in vitro translation of a target mRNA, followed by the size analysis of the nascent chains using a denaturing gel electrophoresis.

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA

The rate of translational elongation is non-uniform. mRNA secondary structure, codon usage and mRNA associated proteins may alter ribosome movement on the ...

isolation-ribosome-bound-nascent-polypeptides-vitro-to-identify

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16.2K ビュー.  Cleveland State University. mRNA上の翻訳停止部位を同定する技術が記載されている。この手順は、変性ゲル電気泳動を用いた初期のチェーンの大きさの分析に続いて標的mRNAのin vitro翻訳、イン時にリボソーム上で蓄積新生ポリペプチドの分離に基づいています。