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It has become clear that the post-embryonic growth and development of plants requires properly controlled short distance cell-to-cell communication not only through the historically well-known phytohormones, but also through secreted small peptide signals. This protocol demonstrates an example of how to isolate small peptides (< 10 daltons) from complex protein mixtures (e.g. cauliflower meristem protein extraction) for MS/MS analysis.

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Proteolytic Fragment Isolation and Analysis (ex. N-terminal GST-tagged CLAVATA3 Protein GST-CLV3)

Plant Science > Plant biochemistry > Protein > Isolation and purification
Author: Jun Ni
Jun NiAffiliation: Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, USA
For correspondence: junni@stanford.edu
Bio-protocol author page: a61
Vol 2, Iss 14, 7/20/2012, 4086 views, 0 Q&A, How to cite
DOI: http://dx.doi.org/10.21769/BioProtoc.232

[Abstract] It has become clear that the post-embryonic growth and development of plants requires properly controlled short distance cell-to-cell communication not only through the historically well-known phytohormones, but also through secreted small peptide signals. This protocol demonstrates an example of how to isolate small peptides (< 10 daltons) from complex protein mixtures (e.g. cauliflower meristem protein extraction) for MS/MS analysis.

Keywords: CLAVATA3, Meristem protein isolation, Proteolytic processing

Materials and Reagents

  1. Glutathione Sepharose 4B (Amersham biosciences , catalog number: 17-0756-01)
  2. Glutathione (Thermo Fisher Scientific, catalog number: 78259)
  3. Protease inhibitor cocktail (Sigma-Aldrich, catalog number: P9599)
  4. Triton X-100 (Pierce, catalog number: 85111)
  5. GST-mCLV3 proteins
  6. Tris-HCl
  7. Hepes (Sigma-Aldrich, catalog number: H3375)
  8. EDTA (Sigma-Aldrich, catalog nummber: ED100g)
  9. Phenylmethylsulfonyl fluoride (Sigma-Aldrich, catalog number: 78830-1G)
  10. Aprotinin (Sigma-Aldrich, catalog number: A4529-1MG)
  11. Chymostatin (Sigma-Aldrich, catalog number: C7268-1MG)
  12. Leupeptin (Sigma-Aldrich, catalog number: L2884-5MG)
  13. Eluting buffer (see Recipes)
  14. Cauliflower extraction buffer (see Recipes)

Equipment

  1. Rotor
  2. Microcon YM-10 centrifugal filter (EMD Millipore)
  3. Tabletop centrifuge
  4. Mass spectrometer (4700 proteomics analyzer)

Procedure

  1. Cauliflower (Brassica oleracea) meristem protein extracts were prepared as described before (Trotochaud et al., 1999) with or without 0.1% Triton X-100. Note that 1 ml of protease inhibitor cocktail for use with plant cell extracts was added in the extraction buffer per 300 x g of tissues. Before use, the extracts were centrifuged at 40,000 x g for 30 min at 4 °C. It is very important to use fresh cauliflower. We usually try to get cauliflower from local farms. The meristem tissues were collected using razor blade “shaving” the head of the cauliflower.

  2. Incubate ~100 μg purified GST-mCLV3 proteins (mature CLV3 protrein) with ~400 μl cauliflower protein extracts for 2 h at room temperature (RT) on a rotor.

  3. For N-terminal tagged fragment (~ 32-34 kD) isolation.
    1. Bound protein mixtures to Glutathione Sepharose 4B.
    2. Elute the N-terminal GST containing fragments from the beads with buffer containing 10 mM Glutathione, 50 mM Tris-HCl (pH 8.0).
    3. If needed, concentrate protein elution using Microcon YM-50 centrifugal filter at 14,000 x g, 4 °C for 30 min and elute in desired volume and buffer (e.g. 0.1% TFA trifluoroacetic acid/water) for MS analysis.

  4. For C-terminal untagged fragment (~ 2-4 kD) isolation.
    1. Subject protein mixtures to centrifuge through Microcon YM-10 centrifugal filter at 14,000 x g, 4 °C for 30 min.
    2. Collect the flow-through fractions for intact MS analysis.
    3. Further characterize peaks of interest by MS/MS analysis (control: Cauliflower protein extracts only; GST-CLV3 incubated with cauliflower extraction buffer).

Recipes

  1. Eluting buffer
    50 mM Tris-HCl
    10 mM reduced glutathione (pH 8.0)
  2. Cauliflower extraction buffer
    50 mM Hepes (pH 7.4)
    10 mM EDTA
    0.1% Triton X-100
    1 mM phenylmethylsulfonyl fluoride
    5 mg/ml aprotinin
    10 mg/ml chymostatin
    1 mg/ml leupeptin
    For extracts without membrane proteins, exclude Triton X-100 from the buffer.

Acknowledgments

This protocol has been adapted from previous publications including Ni and Clark (2006), Ni et al. (2011) and Trotochaud et al. (1999).

References

  1. Ni, J. and Clark, S. E. (2006). Evidence for functional conservation, sufficiency, and proteolytic processing of the CLAVATA3 CLE domain. Plant Physiol 140(2): 726-733.
  2. Ni, J., Guo, Y., Jin, H., Hartsell, J. and Clark, S. E. (2011). Characterization of a CLE processing activity. Plant Mol Biol 75(1-2): 67-75.
  3. Trotochaud, A. E., Hao, T., Wu, G., Yang, Z. and Clark, S. E. (1999). The CLAVATA1 receptor-like kinase requires CLAVATA3 for its assembly into a signaling complex that includes KAPP and a Rho-related protein. Plant Cell 11(3): 393-406.


How to cite this protocol: Ni, J. (2012). Proteolytic Fragment Isolation and Analysis (ex. N-terminal GST-tagged CLAVATA3 Protein GST-CLV3). Bio-protocol 2(14): e232. DOI: 10.21769/BioProtoc.232; Full Text



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