MRNA display

mRNA display is a display technique used for in vitro protein, and/or peptide evolution to create molecules that can bind to a desired target. The process results in translated peptides or proteins that are associated with their mRNA progenitor via a puromycin linkage. The complex then binds to an immobilized target in a selection step (affinity chromatography). The mRNA-protein fusions that bind well are then reverse transcribed to cDNA and their sequence amplified via a polymerase chain reaction. The result is a nucleotide sequence that encodes a peptide with high affinity for the molecule of interest.

Puromycin is an analogue of the 3’ end of a tyrosyl-tRNA with a part of its structure mimics a molecule of adenosine, and the other part mimics a molecule of tyrosine. Compared to the cleavable ester bond in a tyrosyl-tRNA, puromycin has a non-hydrolysable amide bond. As a result, puromycin interferes with translation, and causes premature release of translation products.

Figure 1. mRNA-Polypeptide Fusion Formation. a. Ribosome moves along the mRNA template and nascent peptide is being made. When the ribosome reaches the 3’ end of the template, the fused puromycin will enter the A site of the ribosome. b. The mRNA-polypeptide fusion is released.

All mRNA templates used for mRNA display technology have puromycin at their 3’ end. As translation proceeds, ribosome moves along the mRNA template, and once it reaches the 3’ end of the template, the fused puromycin will enter ribosome’s A site and be incorporated into the nascent peptide. The mRNA-polypeptide fusion is then released from the ribosome (Figure 1).

To synthesize an mRNA-polypeptide fusion, the fused puromycin is not the only modification to the mRNA template.[1] Oligonucleotides and other spacers need to be recruited along with the puromycin to provide flexibility and proper length for the puromycin to enter the A site. Ideally, the linker between the 3’ end of an mRNA and the puromycin has to be flexible and long enough to allow the puromycin to enter the A site upon translation of the last codon. This enables the efficient production of high-quality, full-length mRNA-polypeptide fusion. Rihe Liu et al. optimized the 3’-puromycin oligonucleotide spacer. They reported that dA25 in combination with a Spacer 9 (Glen Research), and dAdCdCP at the 5’ terminus worked the best for the fusion reaction. They found that linkers longer than 40 nucleotides and shorter than 16 nucleotides showed greatly reduced efficiency of fusion formation. Also, when the sequence rUrUP presented adjacent to the puromycin, fusion did not form efficiently.[2]

In addition to providing flexibility and length, the poly dA portion of the linker also allows further purification of the mRNA-polypeptide fusion due to its high affinity for dT cellulose resin.[3] The mRNA-polypeptide fusions can be selected over immobilized selection targets for several rounds with increasing stringency. After each round of selection, those library members that stay bound to the immobilized target are PCR amplified, and non-binders are washed off.

## Contents

* 1 Method
* 2 Advantages
* 3 Application
* 4 See also
* 5 References

## Method

Figure 2. Splint Aid Single Stranded mRNA/DNA T4 DNA Ligase Ligation

The synthesis of an mRNA display library starts from the synthesis of a DNA library. A DNA library for any protein or small peptide of interest can be synthesized by solid-phase synthesis followed by PCR amplification. Usually, each member of this DNA library has a T7 RNA polymerase transcription site and a ribosomal binding site at the 5’ end. The T7 promoter region allows large-scale in vitro T7 transcription to transcribe the DNA library into an mRNA library, which provides templates for the in vitro translation reaction later. The ribosomal binding site in the 5’-untranslated region (5’ UTR) is designed according to the in vitro translation system to be used. There are two popular commercially available in vitro translation systems. One is E. coli S30 Extract System (Promega) that requires a Shine-Dalgarno sequence in the 5’ UTR as a ribosomal binding site;[4] the other one is Red Nova Lysate (Novagen), which needs a ΔTMV ribosomal binding site.

Once the mRNA library is generated, it will be Urea-PAGE purified and ligated using T4 DNA ligase to the DNA spacer linker containing puromycin at the 3’ end. In this ligation step, a piece of mRNA is ligated with a single stranded DNA with the help from T4 DNA ligase. This is not a standard T4 DNA ligase ligation reaction, where two pieces of double stranded DNA are ligated together. To increase the yield of this special ligation, a single stranded DNA splint may be used to aid the ligation reaction. The 5’ terminus of the splint is designed to be complementary to the 3’ end of the mRNA, and the 3’ terminus of the splint is designed to be complementary to the 5’ end of the DNA spacer linker, which usually consists of poly dA nucleotides (Figure 2).

Figure 3. Selection Cycle.

The ligated mRNA-DNA-puromycin library is translated in Red Nova Lysate (Novagen) or E. coli S30 Extract System (Promega), resulting in polypeptides covalently linked in cis to the encoding mRNA. The in vitro translation can also be done in a PURE (protein synthesis using recombinant elements) system. PURE system is an E. coli cell-free translation system in which only essential translation components are present. Some components, such as amino acids and aminoacyl-tRNA synthases (AARSs) can be omitted from the system. Instead, chemically acylated tRNA can be added into the PURE system. It has been shown that some unnatural amino acids, such as N-methyl-amino acid accylated tRNA can be incorporated into peptides or mRNA-polypeptide fusions in a PURE system.[5]

After translation, the single-stranded mRNA portions of the fusions will be converted to heteroduplex of RNA/DNA by reverse transcriptase to eliminate any unwanted RNA secondary structures, and render the nucleic acid portion of the fusion more stable. This step is a standard reverse transcription reaction. For instance, it can be done by using Superscript II (GIBCO-BRL) following the manufacturer’s protocol.

The mRNA/DNA-polypeptide fusions can be selected over immobilized selection targets for several rounds (Figure 3). There might be a relatively high background for the first few rounds of selection, and this can be minimized by increasing selection stringency, such as adjusting salt concentration, amount of detergent, and/or temperature during the target/fusion binding period. Following binding selection, those library members that stay bound to the immobilized target are PCR amplified. The PCR amplification step will enrich the population from the mRNA-display library that has higher affinity for the immobilized target. Error-prone PCR can also be done in between each round of selection to further increase the diversity of the mRNA-display library and reduce background in selection.[6]

A less time-consuming protocol for mRNA display was recently published.[7]

## Advantages

Although there are many other molecular display technologies, such as phage display, bacterial display, yeast display, and ribosome display, mRNA display technology has many advantages over the others.[8] The first three biological display libraries listed have polypeptides or proteins expressed on the respective microorganism’s surface and the accompanying coding information for each polypeptide or protein is retrievable from the microorganism’s genome. However, the library size for these three in vivo display systems is limited by the transformation efficiency of each organism. For example, the library size for phage and bacterial display is limited to 1-10 × 10^9 different members. The library size for yeast display is even smaller. Moreover, these cell-based display system only allow the screening and enrichment of peptides/proteins containing natural amino acids. In contrast, mRNA display and ribosome display are in vitro selection methods. They allow a library size as large as 10^15 different members. The large library size increases the probability to select very rare sequences, and also improves the diversity of the selected sequences. In addition, in vitro selection methods remove unwanted selection pressure, such as poor protein expression, and rapid protein degradation, which may reduce the diversity of the selected sequences. Finally, in vitro selection methods allow the application of in vitro mutagenesis[9] and recombination techniques throughout the selection process.

Although both ribosome display and mRNA display are in vitro selection methods, mRNA display has some advantage over the ribosome display technology.[10] mRNA display utilizes covalent mRNA-polypeptide complexes linked through puromycin; whereas, ribosome display utilizes stalled, noncovalent ribosome-mRNA-polypeptide complexes.[11] For ribosome display, selection stringency is limited to keep ribosome-mRNA-polypeptide in a complex because of the noncovalent ribosome-mRNA-polypeptide complexes. This may cause difficulties in reducing background binding during the selection cycle. Also, the polypeptides under selection in a ribosome display system are attached to an enormous rRNA-protein complex, a ribosome, which has a molecular weight of more than 2,000,000 Da. There might be some unpredictable interaction between the selection target and the ribosome, and this may lead to a loss of potential binders during the selection cycle. In contrast, the puromycin DNA spacer linker used in mRNA display technology is much smaller comparing to a ribosome. This linker may have less chance to interact with an immobilized selection target. Thus, mRNA display technology is more likely to give less biased results.

## Application

In 1997, Roberts and Szostak showed that fusions between a synthetic mRNA and its encoded myc epitope could be enriched from a pool of random sequence mRNA-polypeptide fusions by immunoprecipitation.[6]

Nine years later, Fukuda and colleagues chose mRNA display method for in vitro evolution of single-chain Fv (scFv) antibody fragments.[12] They selected six different scFv mutants with five consensus mutations. However, kinetic analysis of these mutants showed that their antigen-specificity remained similar to that of the wild type. However, they have demonstrated that two of the five consensus mutations were within the complementarity determining regions (CDRs). And they concluded that mRNA display has the potential for rapid artificial evolution of high-affinity diagnostic and therapeutic antibodies by optimizing their CDRs.

Roberts and coworkers have demonstrated that unnatural peptide oligomers consisting of an N-substituted amino acid can be synthesized as mRNA-polypeptide fusions.[13] N-substituted amino acid-containing peptides have been associated with good proteolytic stability and improved pharmacokinetic properties. This work indicates that mRNA display technology has the potential for selecting drug-like peptides for therapeutic usage resistant to proteolysis.[14]

## See also

* Ribosome display
* Protein engineering
* Protein–protein interaction screening

## References

1. ↑ "RNA-peptide fusions for the in vitro selection of peptides and proteins". PNAS 94 (23): 12297–12302. 1997. doi:10.1073/pnas.94.23.12297. PMID 9356443. Bibcode: 1997PNAS...9412297R.
2. ↑ "Optimized synthesis of RNA-protein fusions for in vitro protein selection". RNA-Ligand Interactions Part B. Methods in Enzymology. 318. 2000. pp. 268–93. doi:10.1016/S0076-6879(00)18058-9. ISBN 9780121822194.
3. ↑ "Psoralen photo-crosslinked mRNA–puromycin conjugates: a novel template for the rapid and facile preparation of mRNA–protein fusions". Nucleic Acids Research 28 (18): 83e–83. 2000. doi:10.1093/nar/28.18.e83. PMID 10982894.
4. ↑ "An in vitro polysome display system for identifying ligands from very large peptide libraries". Proc Natl Acad Sci USA 91 (19): 9022–6. 1994. doi:10.1073/pnas.91.19.9022. PMID 7522328. Bibcode: 1994PNAS...91.9022M.
5. ↑ "Messenger RNA-programmed incorporation of multiple N-methyl-amino acids into linear and cyclic peptides". Chemistry & Biology 15 (1): 32–42. January 2008. doi:10.1016/j.chembiol.2007.12.008. PMID 18215771.
6. ↑ 6.0 6.1 "RNA-peptide fusions for the in vitro selection of peptides and proteins". Proc Natl Acad Sci USA 94 (23): 12297–302. 1997. doi:10.1073/pnas.94.23.12297. PMID 9356443. Bibcode: 1997PNAS...9412297R.
7. ↑ "Streamlined Protocol for mRNA Display". ACS Combinatorial Science 15 (2): 77–81. 2013. doi:10.1021/co300135r. PMID 23305392.
8. ↑ Roberts RW (June 1999). "Totally in vitro protein selection using mRNA-protein fusions and ribosome display". Current Opinion in Chemical Biology 3 (3): 268–73. doi:10.1016/S1367-5931(99)80042-8. PMID 10359713.
9. ↑ "Pulsed Electromagnetic Fields Improve Bone Microstructure And Strength In Ovariectomized Rats". PLoS ONE 8 (11): e79377. November 2013. doi:10.1371/journal.pone.0079377. PMID 24244491. Bibcode: 2013PLoSO...879377J.
10. ↑ Gold L (April 2001). "mRNA display: diversity matters during in vitro selection". Proc Natl Acad Sci USA 98 (9): 4825–6. doi:10.1073/pnas.091101698. PMID 11320229. Bibcode: 2001PNAS...98.4825G.
11. ↑ Andrew Buchanan; Lutz Jermutus. "Ribosome Display or Mrna Display Method With Selection for Increased Stability of the Protein". Google Patents. http://www.google.com/patents/US20070298430. Retrieved 9 June 2014.
12. ↑ "In vitro evolution of single-chain antibodies using mRNA display". Nucleic Acids Research 34 (19): e127. 2006. doi:10.1093/nar/gkl618. PMID 17012279.
13. ↑ "Encodamers: unnatural peptide oligomers encoded in RNA". Chemistry & Biology 10 (11): 1043–50. November 2003. doi:10.1016/j.chembiol.2003.11.004. PMID 14652071. http://www.cell.com/cell-chemical-biology/pdf/S1074-5521(03)00249-7.pdf.
14. ↑ White, E. Railey; Sun, Luxin; Ma, Zhong; Beckta, Jason M.; Danzig, Brittany A.; Hacker, David E.; Huie, Melissa; Williams, David C. et al. (2015-05-15). "Peptide Library Approach to Uncover Phosphomimetic Inhibitors of the BRCA1 C-Terminal Domain". ACS Chemical Biology 10 (5): 1198–1208. doi:10.1021/cb500757u. PMID 25654734.

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Proteins: key methods of study

Experimental|

* Protein purification
* Green fluorescent protein
* Western blot
* Protein immunostaining
* Protein sequencing
* Gel electrophoresis/Protein electrophoresis
* Protein immunoprecipitation
* Peptide mass fingerprinting/Protein mass spectrometry
* Dual-polarization interferometry
* Microscale thermophoresis
* Chromatin immunoprecipitation
* Surface plasmon resonance
* Isothermal titration calorimetry
* X-ray crystallography
* Protein NMR
* Cryo-electron microscopy
* Freeze-fracture electron microscopy

Bioinformatics|

* Protein structure prediction
* Protein–protein docking
* Protein structural alignment
* Protein ontology
* Protein–protein interaction prediction

Assay|

* Enzyme assay
* Protein assay
* Secretion assay

Display techniques|

* Bacterial display
* mRNA display
* Phage display
* Ribosome display
* Yeast display

Super-resolution microscopy|

* Photoactivated localization microscopy
* Vertico SMI

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