Abstract
Seeds are a common experimental system for many reasons. Among these: (i) they occupy a major niche in agriculture and human nutrition; (ii) they are a rich source of critical genetic information; and (iii) they are a near-ideal system for the study of phytohormone action or the transition from either dormancy or quiescence to active growth and development. One important component of all of these considerations is occurrence of the highly-abundant seed storage proteins (SSP). While on the one hand the high levels of proteins present in seeds make them attractive subjects, the SSP themselves are anathema to proteomics analyses. Without some sort of pretreatment removal of SSP, they will be virtually the only proteins identified in shotgun proteomics analyses. Here in, we describe and compare several methods commonly used to deplete samples of SSP, present the relatively recent application of combinatorial-ligand random-peptide libraries to seed proteomics studies, and speculate briefly on the short-term future.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Ayala A, Parrado J, Machado A (1998) Use of Rotofor preparative isoelectrofocusing cell in protein purification procedure. Appl Biochem Biotechnol 69:11–16
Bandeira N, Nesvizhskii A, McIntosh M (2011) Advancing next-generation proteomics through computational research. J Proteome Res 10:2895–2895
Barnea E, Sorkin R, Ziv T, Beer I, Admon A (2005) Evaluation of prefractionation methods as a preparatory step for multidimensional based chromatography of serum proteins. Proteomics 5:3367–3375
Bier M (1998) Recycling isoelectric focusing and isotachophoresis. Electrophoresis 19:1057–1063
Boschetti E, Righetti PG (2008a) Hexapeptide combinatorial ligand libraries: the march for the detection of the low-abundance proteome continues. BioTechniques 44:663–665
Boschetti E, Righetti PG (2008b) The ProteoMiner in the proteomic arena: a non-depleting tool for discovering low-abundance species. J Proteomics 71:255–264
Boschetti E, Righetti PG (2009) The art of observing rare protein species in proteomes with peptide ligand libraries. Proteomics 9:1492–1510
Boschetti E, Bindschedler LV, Tang C, Fasoli E, Righetti PG (2009) Combinatorial peptide ligand libraries and plant proteomics: a winning strategy at a price. J Chromatogr A 1216:1215–1222
Brandon DL, Hernlem BJ (2009) Development of monoclonal antibodies specific for Ricinus agglutinins. Food Agric Immunol 20:11–22
Cellar NA, Kuppannan K, Langhorst ML, Ni W, Xu P, Young SA (2008) Cross species applicability of abundant protein depletion columns for ribulose-1,5-bisphosphate carboxylase/oxygenase. J Chromatogr B Analyt Technol Biomed Life Sci 861:29–39
Cellar NA, Karnoup AS, Albers DR, Langhorst ML, Young SA (2009) Immunodepletion of high abundance proteins coupled on-line with reversed-phase liquid chromatography: a two-dimensional LC sample enrichment and fractionation technique for mammalian proteomics. J Chromatogr B Analyt Technol Biomed Life Sci 877:79–85
Chait BT (2011) Mass spectrometry in the postgenomic era. Annu Rev Biochem 80:239–246
Chenau J, Michelland S, Sidibe J, Seve M (2008) Peptides OFFGEL electrophoresis: a suitable pre-analytical step for complex eukaryotic samples fractionation compatible with quantitative iTRAQ labeling. Proteome Sci 6:9
Cox J, Mann M (2011) Quantitative, high-resolution proteomics for data-driven systems biology. Annu Rev Biochem 80:273–299
Doyle JJ, Schuler MA, Godette WD, Zenger V, Beachy RN, Slightom JL (1986) The glycosylated seed storage proteins of Glycine max and Phaseolus vulgaris. Structural homologies of genes and proteins. J Biol Chem 261:9228–9238
Ellis RJ (1979) The most abundant protein in the world. Trends Biochem Sci 4:241–244
Elschenbroich S, Ignatchenko V, Sharma P, Schmitt-Ulms G, Gramolini AO, Kislinger T (2009) Peptide separations by on-line MudPIT compared to isoelectric focusing in an off-gel format: application to a membrane-enriched fraction from C2C12 mouse skeletal muscle cells. J Proteome Res 8:4860–4869
Esen A (1990) An immunodominant site of gamma-zein1 is in the region of tandem hexapeptide repeats. J Protein Chem 9:453–460
Fasoli E, D’Amato A, Kravchuk AV, Boschetti E, Bachi A, Righetti PG (2011) Popeye strikes again: the deep proteome of spinach leaves. J Proteomics 74:127–136
Feeney KA, Wellner N, Gilbert SM, Halford NG, Tatham AS, Shewry PR, Belton PS (2003) Molecular structures and interactions of repetitive peptides based on wheat glutenin subunits depend on chain length. Biopolymers 72:123–131
Field JM, Shewry PR, Miflin BJ (1983) Aggregation states of alcohol-soluble storage proteins of barley, rye, wheat and maize. J Sci Food Agric 34:362–369
Gibbs PE, Strongin KB, McPherson A (1989) Evolution of legume seed storage proteins—a domain common to legumins and vicilins is duplicated in vicilins. Mol Biol Evol 6:614–623
Hirabayashi J (2004) Lectin-based structural glycomics: glycoproteomics and glycan profiling. Glycoconj J 21:35–40
Hochstrasser AC, James RW, Pometta D, Hochstrasser D (1991) Preparative isoelectrofocusing and high resolution 2-dimensional gel electrophoresis for concentration and purification of proteins. Appl Theor Electrophor 1:333–337
Hortin GL, Sviridov D (2010) The dynamic range problem in the analysis of the plasma proteome. J Proteomics 73:629–636
Houston NL, Hajduch M, Thelen JJ (2009) Quantitative proteomics of seed filling in castor: comparison with soybean and rapeseed reveals differences between photosynthetic and nonphotosynthetic seed metabolism. Plant Physiol 151:857–868
Hörth P, Miller CA, Preckel T, Wenz C (2006) Efficient fractionation and improved protein identification by peptide OFFGEL electrophoresis. Mol Cell Proteomics 5:1968–1974
Krishnan HB, Natarajan SS (2009) A rapid method for depletion of rubisco from soybean (Glycine max) leaf for proteomic analysis of lower abundance proteins. Phytochemistry 70:1958–1964
Krishnan HB, Oehrle NW, Natarajan SS (2009) A rapid and simple procedure for the depletion of abundant storage proteins from legume seeds to advance proteome analysis: a case study using Glycine max. Proteomics 9:3174–3188
Krishnan HB (2000) Biochemistry and molecular biology of soybean seed storage proteins. J New Seeds 2:1–25
Lauer I, Foetisch K, Kolarich D, Ballmer-Weber BK, Conti A, Altmann F, Vieths S, Scheurer S (2004) Hazelnut (Corylus avellana) vicilin Cor a11: molecular characterization of a glycoprotein and its allergenic activity. Biochem J 383:327–334
Lerouge P, Cabanes-Macheteau M, Rayon C, Fischette-Lainé AC, Gomord V, Faye L (1998) N-glycoprotein biosynthesis in plants: recent developments and future trends. Plant Mol Biol 38:31–48
Lis H, Sharon N (1973) The biochemistry of plant lectins (phytohemagglutinins). Annu Rev Biochem 42:541–574
Maruyama N, Katsube T, Wada Y, Oh MH, Barba De La Rosa AP, Okuda E, Nakagawa S, Utsumi S (1998) The roles of the N-linked glycans and extension regions of soybean beta-conglycinin in folding, assembly and structural features. Eur J Biochem 258:854–862
Miernyk JA, Hajduch M (2011) Seed proteomics. J Proteomics 74:389–400
Miernyk JA, Johnston ML (2006) Chemical cross-linking immobilized concanavalin A for use in proteomic analyses. Prep Biochem Biotechnol 36:203–214
Miernyk JA, Preťová A, Olmedilla A, Klubicova K, Obert B, Hajduch M (2011) Using proteomics to study sexual reproduction in angiosperms. Sexual Plant Reprod 24:9–22
Ogata Y, Charlesworth MC, Muddiman DC (2005) Evaluation of protein depletion methods for the analysis of total-, phospho- and glycoproteins in lumbar cerebrospinal fluid. J Proteome Res 4:837–845
Osborne TB (1908) Our present knowledge of plant proteins. Science 28:417–427
Parry MA, Andralojc PJ, Mitchell RA, Madgwick PJ, Keys AJ (2003) Manipulation of rubisco: the amount, activity, function and regulation. J Exp Bot 54:1321–1333
Petrash JM, DeLucas LJ, Bowling E, Egen N (1991) Resolving isoforms of aldose reductase by preparative isoelectric focusing in the Rotofor. Electrophoresis 12:84–90
Richardson MR, Liu S, Ringham HN, Chan V, Witzmann FA (2008) Sample complexity reduction for two-dimensional electrophoresis using solution isoelectric focusing prefractionation. Electrophoresis 29:2637–2644
Righetti PG, Boschetti E, Monsarrat B (2007) The “invisible proteome”: how to capture the low abundance proteins via combinatorial ligand libraries. Curr Proteomics 4:198–208
Righetti PG, Boschetti E, Zanella A, Fasoli E, Citterio A (2010) Plucking, pillaging and plundering proteomes with combinatorial peptide ligand libraries. J Chromatogr A 1217:893–900
Righetti PG, Castagna A, Herbert B, Reymond F, Rossier JS (2003) Prefractionation techniques in proteome analysis. Proteomics 3:1397–1407
Rüdiger H, Gabius HJ (2001) Plant lectins: occurrence, biochemistry, functions and applications. Glycoconj J 18:589–613
Schneider C, Newman RA, Sutherland DR, Asser U, Greaves MF (1982) A one-step purification of membrane proteins using a high efficiency immunomatrix. J Biol Chem 257:10766–10769
Scruggs SB, Reisdorph R, Armstrong ML, Warren CM, Reisdorph N, Solaro RJ, Buttrick PM (2010) A novel, in-solution separation of endogenous cardiac sarcomeric proteins and identification of distinct charged variants of regulatory light chain. Mol Cell Proteomics 9:1804–1818
Shewry PR, Napier JA, Tatham AS (1995) Seed storage proteins: structures and biosynthesis. Plant Cell 7:945–956
Steel LF, Trotter MG, Nakajima PB, Mattu TS, Gonye G, Block T (2003) Efficient and specific removal of albumin from human serum samples. Mol Cell Proteomics 2:262–270
Thorsell A, Portelius E, Blennow K, Westman-Brinkmalm A (2007) Evaluation of sample fractionation using micro-scale liquid-phase isoelectric focusing on mass spectrometric identification and quantitation of proteins in a SILAC experiment. Rapid Commun Mass Spectrom 21;771–778
Van Damme EJ (2011) Lectins as tools to select for glycosylated proteins. Methods Mol Biol 753:289–297
Vestal ML (2011) The future of biological mass spectrometry. J Am Soc Mass Spectrom 22:953–959
Vincent D, Balesdent MH, Gibon J, Claverol S, Lapaillerie D, Lomenech AM, Blaise F, Rouxel T, Martin F, Bonneu M, Amselem J, Dominguez V, Howlett BJ, Wincker P, Joets J, Lebrun MH, Plomion C (2009) Hunting down fungal secretomes using liquid-phase IEF prior to high resolution 2-DE. Electrophoresis 32:4118–4136
Wagner L, Wermann M, Rosche F, Rahfeld JU, Hoffmann T, Demuth HU (2011) Isolation of dipeptidyl peptidase IV (DP 4) isoforms from porcine kidney by preparative isoelectric focusing to improve crystallization. Biol Chem 392:665–677
Wilson IB (2002) Glycosylation of proteins in plants and invertebrates. Curr Opin Struct Biol 12:569–577
Wu L, Han DK (2006) Overcoming the dynamic range problem in mass spectrometry-based shotgun proteomics. Expert Rev Proteomics 3:611–619
Zolotarjova N, Martosella J, Nicol G, Bailey J, Boyes BE, Barrett WC (2005) Differences among techniques for high-abundant protein depletion. Proteomics 5:3304–3313
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2012 Springer Science+Business Media Dordrecht
About this chapter
Cite this chapter
Miernyk, J.A., Johnston, M.L. (2012). Digging Deeper into the Seed Proteome: Prefractionation of Total Proteins. In: Agrawal, G., Rakwal, R. (eds) Seed Development: OMICS Technologies toward Improvement of Seed Quality and Crop Yield. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-4749-4_14
Download citation
DOI: https://doi.org/10.1007/978-94-007-4749-4_14
Published:
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-007-4748-7
Online ISBN: 978-94-007-4749-4
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)