Materials and Reagents

Bodicon m7G capping system (Bodicon, catalog number: CS0130 )
S-adenosyl methionine (SAM) (involved in Bodicon m7G capping system) (Bodicon, catalog number: CS0130)
Bodicon Capping Enzyme (10 U/µl) (involved in Bodicon m7G capping system) (Bodicon, catalog number: CS0130)
Note: Because the sale of this kit was low, the previous companies which provided this capping kit were out of service. This capping kit was provided by a new company in China as custom-made products (contact e-mail: service@bodicon.cn, phone:+86-13628662011). In fact the similar capping kit from any other companies (such as EPICENTRE biotechnologies, ScriptCap m7G capping system, catalog number: SCCE0610 ) is suitable for this experiment, and people can also contact with us to get the related protein or kit.
Inorganic pyrophospatase (YIPP) (New England Biolabs, catalog number: M2403S )
S-adenosyl [methyl-³H] methionine ([³H]-SAM) (PerkinElmer, catalog number: NET155H001MC )
DEAE Sephadex (GE Healthcare, catalog number: 17-0170-01 )
GTP (Thomas Scientific, catalog number: R0461 )
RNase inhibitor (Thomas Scientific, catalog number: EO0381 )
RNase free water
Phenol-chloroform (pH 4.8-5.2 for RNA only)
Ethanol (RNase free)
RNase free water
Sodium Dodecyl Sulfonate (SDS)
Ethylene Diamine Tetraacetic Acid (EDTA)
NH₄HCO₃
NaCl
10x MTase Buffer (see Recipes)
Cap-0 cap structure (m7GpppN-RNA) (see Recipes)
Non-methylated Cap-0 cap structure (GpppN-RNA) (see Recipes)
MTase assay reaction mix (see Recipes)

Equipment

Bechtop
Water bath
Centrifuge
Liquid scintillation counter

Procedure

Synthesis of RNA cap structure as substrates.
The nascent RNA transcribed in vitro possesses a 5' triphosphate end. Two RNA capping systems are used to synthesize cap structure as the substrates of MTase.

Combine 1-10 µg RNA and RNase free water up to 12.5 µl of total reaction volume.
To heat to denature the in vitro transcribed RNA, incubate the tube at 65 °C for 10 min, and transfer the tube to ice immediately.

Combine the following reaction components in the order given:

Cap-0 cap structure (m7GpppN-RNA)
Heat denatured RNA	12.5 µl
10x Bodicon Capping Buffer	2 µl
10 mM GTP	2 µl
3 mM SAM	1 µl
RNase inhibitor 40 U/µl	0.5 µl
Bodicon Capping Enzyme (10 U/µl)	2 µl
Total	20 µl
Non-methylated Cap-0 cap structure (GpppN-RNA)
Heat denatured RNA	12.5 µl
10x Bodicon Capping Buffer	2 µl
10 mM GTP	2 µl
Inorganic pyrophospatase 0.1 U/µl	1 µl
RNase inhibitor 40 U/µl	0.5 µl
Bodicon Capping Enzyme (10 U/µl)	2 µl
Total	20 µl

Incubate at 37 °C for 2 h.
Purify the RNA substrates by using phenol-chloroform extraction and ethanol precipitation methods.

Prepare 10x MTase Buffer. The MTase buffer may be changed depending on different interested MTases.

Combine the following reaction components in the order given for MTase assays:

Purified MTases	1 µg
10x MTase Buffer	3 μl
GpppN-RNA or m7GpppN-RNA	2 μg
3 mM SAM	0.5 μl
[³H]-SAM (67.3 Ci/mmol, 0.5 μCi/μl)	1 μl
RNase inhibitor 40 U/μl	1 μl
RNase free water	up to 30 μl
Total	30 μl

Incubate the reaction at 30-37 °C depending on different MTases for 1.5 h.
Transfer the tubes onto ice and add equal volume (30 μl) of 0.2% SDS, 20 mM EDTA.
Keep the tubes on ice, add 1 ml of 10 mM NH₄HCO₃ (pH 8.5).
Prepare 1 ml DEAE Sephadex column and equilibrated with 10 ml 10 mM NH₄HCO₃ (pH 8.5).
Load the samples onto the equilibrated column.
Wash the column with 10 ml of 10 mM NH₄HCO₃ (pH 8.5), 100 mM NaCl.
Elute the samples with 1.5 ml of 10 mM NH₄HCO₃ (pH 8.5), 400 mM NaCl.
Add equal volume scintillation liquid, mix well by vortexing and measure the signal using Liquid scintillation counter. The counting signal of [³H], which is transformed from [³H]-SAM to RNA substrates, represents the activity of tested MTases.

Recipes

10x MTase Buffer
0.5 M Tris-HCl (pH 7.5 or 8.0)
50 mM KCl
20 mM MgCl₂
20 mM DTT

Cap-0 cap structure (m7GpppN-RNA)

Heat denatured RNA	13.5 µl
10x Bodicon Capping Buffer	2 µl
10 mM GTP	2 µl
3 mM SAM	1 µl
RNase inhibitor 40 U/µl	0.5 µl
Bodicon Capping Enzyme (10 U/µl)	2 µl
Total	20 µl

Non-methylated Cap-0 cap structure (GpppN-RNA)

Heat denatured RNA	13.5 µl
10x Bodicon Capping Buffer	2 µl
10 mM GTP	2 µl
Inorganic pyrophospatase 0.1 U/µl	1 µl
RNase inhibitor 40 U/µl	0.5 µl
Bodicon Capping Enzyme (10 U/µl)	2 µl
Total	20 µl

MTase assay reaction mix

Purified MTases	1 µg
10x MTase Buffer	3 μl
GpppN-RNA or m7GpppN-RNA	2 μg
3 mM SAM	0.5 μl
[³H]-SAM (67.3 Ci/mmol, 0.5 μCi/μl)	1 μl
RNase inhibitor 40 U/μl	1 μl
RNase free waterup to	30 μl
Total	30 μl

Acknowledgments

We thank Dr. Tero Ahola from University of Helsinki for the kindly help and advices for setting up this MTase assay. We thankfully acknowledge the University of Helsinki for providing research facilities and support during our visits. This work was supported by the China NSFC grants (81130083, 31170152 and 81271817).

References

Chen, Y., Tao, J., Sun, Y., Wu, A., Su, C., Gao, G., Cai, H., Qiu, S., Wu, Y., Ahola, T. and Guo, D. (2013). Structure-function analysis of severe acute respiratory syndrome coronavirus RNA cap guanine-N7-methyltransferase. J Virol 87(11): 6296-6305.
Chen, Y., Su, C., Ke, M., Jin, X., Xu, L., Zhang, Z., Wu, A., Sun, Y., Yang, Z., Tien, P., Ahola, T., Liang, Y., Liu, X. and Guo, D. (2011). Biochemical and structural insights into the mechanisms of SARS coronavirus RNA ribose 2'-O-methylation by nsp16/nsp10 protein complex. PLoS Pathog 7(10): e1002294.
Chen, Y., Cai, H., Pan, J., Xiang, N., Tien, P., Ahola, T. and Guo, D. (2009). Functional screen reveals SARS coronavirus nonstructural protein nsp14 as a novel cap N7 methyltransferase. Proc Natl Acad Sci U S A 106(9): 3484-3489.