The physiology and proteomics of drought tolerance in maize: early stomatal closure as a cause of lower tolerance to short-term dehydration?

. 2012 ; 7 (6) : e38017. [epub] 20120613

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid22719860

Understanding the response of a crop to drought is the first step in the breeding of tolerant genotypes. In our study, two maize (Zea mays L.) genotypes with contrasting sensitivity to dehydration were subjected to moderate drought conditions. The subsequent analysis of their physiological parameters revealed a decreased stomatal conductance accompanied by a slighter decrease in the relative water content in the sensitive genotype. In contrast, the tolerant genotype maintained open stomata and active photosynthesis, even under dehydration conditions. Drought-induced changes in the leaf proteome were analyzed by two independent approaches, 2D gel electrophoresis and iTRAQ analysis, which provided compatible but only partially overlapping results. Drought caused the up-regulation of protective and stress-related proteins (mainly chaperones and dehydrins) in both genotypes. The differences in the levels of various detoxification proteins corresponded well with the observed changes in the activities of antioxidant enzymes. The number and levels of up-regulated protective proteins were generally lower in the sensitive genotype, implying a reduced level of proteosynthesis, which was also indicated by specific changes in the components of the translation machinery. Based on these results, we propose that the hypersensitive early stomatal closure in the sensitive genotype leads to the inhibition of photosynthesis and, subsequently, to a less efficient synthesis of the protective/detoxification proteins that are associated with drought tolerance.

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Farooq M, Wahid A, Kobayashi N, Fujita D, Basra SMA. Plant drought stress: effects, mechanisms and management. Agron Sustain Dev. 2009;29:185– 212.

Pinheiro C, Chaves MM. Photosynthesis and drought: can we make metabolic connections from available data? J Exp Bot. 2011;62:869– 882. PubMed

Chernyad’ev II. Effect of water stress on the photosynthetic apparatus of plants and the protective role of cytokinins: A review. Appl Biochem Microbiol. 2005;41:115– 128. PubMed

Medrano H, Escalona JM, Bota J, Gulias J, Flexas J. Regulation of photosynthesis of C-3 plants in response to progressive drought: Stomatal conductance as a reference parameter. Ann Bot. 2002;89:895– 905. PubMed PMC

Pospisilova J, Vagner M, Malbeck J, Travniakova A, Batkova P. Interactions between abscisic acid and cytokinins during water stress and subsequent rehydration. Biol Plant. 2005;49:533– 540.

Seki M, Umezawa T, Kim JM, Matsui A, To T, et al. Jenks MA, Hasegawa PM, Jain SM, editors. Transcriptome analysis of plant drought and salt stress response. 2007. pp. 261– 283. Advances in Molecular Breeding Toward Drought and Salt Tolerant Crops. New York: Springer.

Wilkinson S, Davies WJ. ABA-based chemical signalling: the co-ordination of responses to stress in plants. Plant Cell Environ. 2002;25:195– 210. PubMed

Wilkinson S, Davies WJ. Drought, ozone, ABA and ethylene: new insights from cell to plant to community. Plant Cell Environ. 2010;33:510– 525. PubMed

Chaves MM, Flexas J, Pinheiro C. Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot. 2009;103:551– 560. PubMed PMC

Lawlor DW, Tezara W. Causes of decreased photosynthetic rate and metabolic capacity in water-deficient leaf cells: a critical evaluation of mechanisms and integration of processes. Ann Bot. 2009;103:561– 579. PubMed PMC

Lopes MS, Araus JL, van Heerden PDR, Foyer CH. Enhancing drought tolerance in C(4) crops. J Exp Bot. 2011;62:3135– 3153. PubMed

Chaves MM, Maroco JP, Pereira JS. Understanding plant responses to drought - from genes to the whole plant. Funct Plant Biol. 2003;30:239– 264. PubMed

Flexas J, Medrano H. Drought-inhibition of photosynthesis in C-3 plants: Stomatal and non-stomatal limitations revisited. Ann Bot. 2002;89:183– 189. PubMed PMC

Flexas J, Bota J, Loreto F, Cornic G, Sharkey TD. Diffusive and metabolic limitations to photosynthesis under drought and salinity in C(3) plants. Plant Biol. 2004;6:269– 279. PubMed

Lawlor DW. Limitation to photosynthesis in water-stressed leaves: Stomata vs. metabolism and the role of ATP. Ann Bot. 2002;89:871– 885. PubMed PMC

Yordanov I, Velikova V, Tsonev T. Plant responses to drought and stress tolerance. Bulg J Plant Physiol 187–206. 2003.

Parry MAJ, Andralojc PJ, Khan S, Lea PJ, Keys AJ. Rubisco activity: Effects of drought stress. Ann Bot. 2002;89:833– 839. PubMed PMC

Reddy AR, Chaitanya KV, Vivekanandan M. Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J Plant Physiol. 2004;161:1189– 1202. PubMed

Lawlor DW, Cornic G. Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ. 2002;25:275– 294. PubMed

Ghannoum O. C(4) photosynthesis and water stress. Ann Bot. 2009;103:635– 644. PubMed PMC

Cornic G, Fresneau C. Photosynthetic carbon reduction and carbon oxidation cycles are the main electron sinks for photosystem II activity during a mild drought. Ann Bot. 2002;89:887– 894. PubMed PMC

Chaves MM, Pereira JS, Maroco J, Rodrigues ML, Ricardo CPP, et al. How plants cope with water stress in the field. Photosynthesis and growth. Ann Bot. 2002;89:907– 916. PubMed PMC

Langridge P, Paltridge N, Fincher G. Functional genomics of abiotic stress tolerance in cereals. Brief Funct Genomics Proteomics. 2006;4:343– 354. PubMed

Valliyodan B, Nguyen HT. Understanding regulatory networks and engineering for enhanced drought tolerance in plants. Curr Opin Plant Biol. 2006;9:189– 195. PubMed

Verbruggen N, Hermans C. Proline accumulation in plants: a review. Amino Acids. 2008;35:753– 759. PubMed

Bray EA. Jenks MA, Hasegawa PM, Jain SM, editors. Molecular and physiological responses to water-deficit stress. 2007. Advances in Molecular Breeding Toward Drought and Salt Tolerant Crops. New York: Springer.

Cohen D, Bogeat-Triboulot MB, Tisserant E, Balzergue S, Martin-Magniette ML, et al. Comparative transcriptomics of drought responses in Populus: a meta-analysis of genome-wide expression profiling in mature leaves and root apices across two genotypes. BMC Genomics 11. 2010. PubMed PMC

Gong PJ, Zhang JH, Li HX, Yang CX, Zhang CJ, et al. Transcriptional profiles of drought-responsive genes in modulating transcription signal transduction, and biochemical pathways in tomato. J Exp Bot. 2010;61:3563– 3575. PubMed PMC

Hayano-Kanashiro C, Calderon-Vazquez C, Ibarra-Laclette E, Herrera-Estrella L, Simpson J. Analysis of Gene Expression and Physiological Responses in Three Mexican Maize Landraces under Drought Stress and Recovery Irrigation. PLoS ONE 4. 2009. PubMed PMC

Matsui A, Ishida J, Morosawa T, Mochizuki Y, Kaminuma E, et al. Arabidopsis transcriptome analysis under drought, cold, high-salinity and ABA treatment conditions using a tiling array. Plant Cell Physiol. 2008;49:1135– 1149. PubMed

Seki M, Narusaka M, Ishida J, Nanjo T, Fujita M, et al. Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high-salinity stresses using a full-length cDNA microarray. Plant J. 2002;31:279– 292. PubMed

Shinozaki K, Yamaguchi-Shinozaki K. Gene networks involved in drought stress response and tolerance. J Exp Bot. 2007;58:221– 227. PubMed

Zheng J, Zhao JF, Tao YZ, Wang JH, Liu YJ, et al. Isolation and analysis of water stress induced genes in maize seedlings by subtractive PCR and cDNA macroarray. Plant Mol Biol. 2004;55:807– 823. PubMed

Bogeat-Triboulot MB, Brosche M, Renaut J, Jouve L, Le Thiec D, et al. Gradual soil water depletion results in reversible changes of gene expression, protein profiles, ecophysiology, and growth performance in Populus euphratica, a poplar growing in arid regions. Plant Physiol. 2007;143:876– 892. PubMed PMC

Kottapalli KR, Rakwal R, Shibato J, Burow G, Tissue D, et al. Physiology and proteomics of the water-deficit stress response in three contrasting peanut genotypes. Plant Cell Environ. 2009;32:380– 407. PubMed

Peng ZY, Wang MC, Li F, Lu HJ, Li CL, et al. A Proteomic Study of the Response to Salinity and Drought Stress in an Introgression Strain of Bread Wheat. Mol Cell Proteom. 2009;8:2676– 2686. PubMed PMC

Ali GM, Komatsu S. Proteomic analysis of rice leaf sheath during drought stress. J Proteome Res. 2006;5:396– 403. PubMed

Ke YQ, Han GQ, He HQ, Li JX. Differential regulation of proteins and phosphoproteins in rice under drought stress. Biochem Biophys Res Commun. 2009;379:133– 138. PubMed

Salekdeh GH, Siopongco J, Wade LJ, Ghareyazie B, Bennett J. Proteomic analysis of rice leaves during drought stress and recovery. Proteomics. 2002;2:1131– 1145. PubMed

Salekdeh GH, Siopongco J, Wade LJ, Ghareyazie B, Bennett J. A proteomic approach to analyzing drought- and salt-responsiveness in rice. Field Crops Res. 2002;76:199– 219.

Shu LB, Ding W, Wu JH, Feng FJ, Luo LJ, et al. Proteomic Analysis of Rice Leaves Shows the Different Regulations to Osmotic Stress and Stress Signals. J Integr Plant Biol. 2010;52:981– 995. PubMed

Xiong JH, Fu BY, Xu HX, Li YS. Proteomic analysis of PEG-simulated drought stress-responsive proteins of rice leaves using a pyramiding rice line at the seedling stage. Bot Stud. 2010;51:137– 145.

de Vienne D, Leonardi A, Damerval C, Zivy M. Genetics of proteome variation for QTL characterization: application to drought-stress responses in maize. J Exp Bot. 1999;50:303– 309.

Mohammadkhani N, Heidari R. Effects of drought stress on soluble proteins in two maize varieties. Turk J Biol. 2008;32:23– 30.

Riccardi F, Gazeau P, de Vienne D, Zivy M. Protein changes in response to progressive water deficit in maize - Quantitative variation and polypeptide identification. Plant Physiol. 1998;117:1253– 1263. PubMed PMC

Riccardi F, Gazeau P, Jacquemot MP, Vincent D, Zivy M. Deciphering genetic variations of proteome responses to water deficit in maize leaves. Plant Physiol Biochem. 2004;42:1003– 1011. PubMed

Tai FJ, Yuan ZL, Wu XL, Zhao PF, Hu XL, et al. Identification of membrane proteins in maize leaves, altered in expression under drought stress through polyethylene glycol treatment. Plant Omics. 2011;4:250– 256.

Vincent D, Lapierre C, Pollet B, Cornic G, Negroni L, et al. Water deficits affect caffeate O-methyltransferase, lignification, and related enzymes in maize leaves. A proteomic investigation. Plant Physiol. 2005;137:949– 960. PubMed PMC

Caruso G, Cavaliere C, Foglia P, Gubbiotti R, Samperi R, et al. Analysis of drought responsive proteins in wheat (Triticum durum) by 2D-PAGE and MALDI-TOF mass spectrometry. Plant Sci. 2009;177:570– 576.

Parida AK, Dagaonkar VS, Phalak MS, Umalkar GV, Aurangabadkar LP. Alterations in photosynthetic pigments, protein and osmotic components in cotton genotypes subjected to short-term drought stress followed by recovery. Plant Biotechnol Rep. 2007;1:37– 48.

Huerta-Ocampo JA, Briones-Cerecero EP, Mendoza-Hernandez G, De Leon-Rodriguez A, de la Rosa APB. Proteomic Analysis of Amaranth (Amaranthus Hypochondriacus L.) Leaves Under Drought Stress. Int J Plant Sci. 2009;170:990– 998.

Aranjuelo I, Molero G, Erice G, Avice JC, Nogues S. Plant physiology and proteomics reveals the leaf response to drought in alfalfa (Medicago sativa L.). J Exp Bot. 2011;62:111– 123. PubMed PMC

Hajheidari M, Abdollahian-Noghabi M, Askari H, Heidari M, Sadeghian SY, et al. Proteome analysis of sugar beet leaves under drought stress. Proteomics. 2005;5:950– 960. PubMed

Fulda S, Mikkat S, Stegmann H, Horn R. Physiology and proteomics of drought stress acclimation in sunflower (Helianthus annuus L.). Plant Biol. 2011;13:632– 642. PubMed

Bonhomme L, Monclus R, Vincent D, Carpin S, Claverol S, et al. Genetic variation and drought response in two Populus x euramericana genotypes through 2-DE proteomic analysis of leaves from field and glasshouse cultivated plants. Phytochemistry. 2009;70:988– 1002. PubMed

Xiao XW, Yang F, Zhang S, Korpelainen H, Li CY. Physiological and proteomic responses of two contrasting Populus cathayana populations to drought stress. Physiol Plant. 2009;136:150– 168. PubMed

Xu CP, Huang BR. Comparative Analysis of Drought Responsive Proteins in Kentucky Bluegrass Cultivars Contrasting in Drought Tolerance. Crop Sci. 2010;50:2543– 2552.

Xu CP, Huang BR. Differential proteomic responses to water stress induced by PEG in two creeping bentgrass cultivars differing in stress tolerance. J Plant Physiol. 2010;167:1477– 1485. PubMed

Zhao Y, Du HM, Wang ZL, Huang BR. Identification of proteins associated with water-deficit tolerance in C(4) perennial grass species, Cynodon dactylon x Cynodon transvaalensis and Cynodon dactylon. Physiol Plant. 2011;141:40– 55. PubMed

Ashraf M. Inducing drought tolerance in plants: Recent advances. Biotechnol Adv. 2010;28:169– 183. PubMed

Salekdeh GH, Komatsu S. Crop proteomics: Aim at sustainable agriculture of tomorrow. Proteomics. 2007;7:2976– 2996. PubMed

Shao HB, Chu LY, Jaleel CA, Manivannan P, Panneerselvam R, et al. Understanding water deficit stress-induced changes in the basic metabolism of higher plants - biotechnologically and sustainably improving agriculture and the ecoenvironment in arid regions of the globe. Crit Rev Biotechnol. 2009;29:131– 151. PubMed

Tardieu F. Any trait or trait-related allele can confer drought tolerance: just design the right drought scenario. J Exp Bot. 2012;63:25– 31. PubMed

Ribaut JM, Betran J, Monneveux P, Setter T. Bennetzen JL, Hake SC, editors. Drought tolerance in maize. 2012. pp. 311– 344. Handbook of Maize: Its Biology. New York: Springer.

Cattivelli L, Rizza F, Badeck FW, Mazzucotelli E, Mastrangelo AM, et al. Drought tolerance improvement in crop plants: An integrated view from breeding to genomics. Field Crops Res. 2008;105:1– 14.

Grzesiak MT, Grzesiak S, Skoczowski A. Changes of leaf water potential and gas exchange during and after drought in triticale and maize genotypes differing in drought tolerance. Photosynthetica. 2006;44:561– 568.

Grzesiak MT, Rzepka A, Hura T, Hura K, Skoczowski A. Changes in response to drought stress of triticale and maize genotypes differing in drought tolerance. Photosynthetica. 2007;45:280– 287.

Kumari M, Dass S, Vimala Y, Arora P. Physiological parameters governing drought tolerance in maize. Indian J Plant Physiol. 2004;9:203– 207.

Zarco-Perelló E, Gonzáles-Hernández VA, López-Peralta MC, Sallinas-Moreno Y. Physiological markers for drought tolerance in maize (Zea mays L.). Agrociencia. 2005;39:517– 528.

Fenta BA, Driscoll SP, Kunert KJ, Foyer CH. Characterization of drought-tolerance traits in nodulated soya beans: The importance of maintaining photosynthesis and shoot biomass under drought-induced limitations on nitrogen metabolism. J Agron Crop Sci. 2012;198:92– 103.

Taylor NL, Tan YF, Jacoby RP, Millar AH. Abiotic environmental stress induced changes in the Arabidopsis thaliana chloroplast, mitochondria and peroxisome proteomes. J Proteomics. 2009;72:367– 378. PubMed

Bonhomme L, Monclus R, Vincent D, Carpin S, Lomenech AM, et al. Leaf proteome analysis of eight Populus xeuramericana genotypes: Genetic variation in drought response and in water-use efficiency involves photosynthesis-related proteins. Proteomics. 2009;9:4121– 4142. PubMed

Close TJ. Dehydrins: Emergence of a biochemical role of a family of plant dehydration proteins. Physiol Plant. 1996;97:795– 803.

Cellier F, Conejero G, Breitler JC, Casse F. Molecular and physiological responses to water deficit in drought-tolerant and drought-sensitive lines of sunflower - Accumulation of dehydrin transcripts correlates with tolerance. Plant Physiol. 1998;116:319– 328. PubMed PMC

Wood AJ, Goldsbrough PB. Characterization and expression of dehydrins in water-stressed Sorghum bicolor. Physiol Plant. 1997;99:144– 152.

Veeranagamallaiah G, Prasanthi J, Reddy KE, Pandurangaiah M, Babu OS, et al. Group 1 and 2 LEA protein expression correlates with a decrease in water stress induced protein aggregation in horsegram during germination and seedling growth. J Plant Physiol. 2011;168:671– 677. PubMed

Lascano HR, Antonicelli GE, Luna CM, Melchiorre MN, Gomez LD, et al. Antioxidant system response of different wheat cultivars under drought: field and in vitro studies. Austr J Plant Physiol. 2001;28:1095– 1102.

Loggini B, Scartazza A, Brugnoli E, Navari-Izzo F. Antioxidative defense system, pigment composition, and photosynthetic efficiency in two wheat cultivars subjected to drought. Plant Physiol. 1999;119:1091– 1099. PubMed PMC

Sairam RK, Saxena DC. Oxidative stress and antioxidants in wheat genotypes: Possible mechanism of water stress tolerance. J Agron Crop Sci. 2000;184:55– 61.

Pastori GM, Trippi VS. Oxidative Stress Induces High-Rate of Glutathione-Reductase Synthesis in A Drought-Resistant Maize Strain. Plant Cell Physiol. 1992;33:957– 961.

Guo Z, Ou W, Lu S, Zhong Q. Differential responses of antioxidative system to chilling and drought in four rice cultivars differing in sensitivity. Plant Physiol Biochem. 2006;44:828– 836. PubMed

Arcy-Lameta A, Ferrari-Iliou R, Contour-Ansel D, Pham-Thi AT, Zuily-Fodil Y. Isolation and characterization of four ascorbate peroxidase cDNAs responsive to water deficit in cowpea leaves. Ann Bot. 2006;97:133– 140. PubMed PMC

Contour-Ansel D, Torres-Franklin ML, De Carvalho MHC, Arcy-Lameta A. Glutathione reductase in leaves of cowpea: Cloning of two cDNAs, expression and enzymatic activity under progressive drought stress, desiccation and abscisic acid treatment. Ann Bot. 2006;98:1279– 1287. PubMed PMC

Torres-Franklin ML, Contour-Ansel D, Zuily-Fodil Y, Pham-Thi AT. Molecular cloning of glutathione reductase cDNAs and analysis of GR gene expression in cowpea and common bean leaves during recovery from moderate drought stress. J Plant Physiol. 2008;165:514– 521. PubMed

Turkan I, Bor M, Ozdemir F, Koca H. Differential responses of lipid peroxidation and antioxidants in the leaves of drought-tolerant P-acutifolius Gray and drought-sensitive P-vulgaris L. subjected to polyethylene glycol mediated water stress. Plant Sci. 2005;168:223– 231.

Edjolo A, Laffray D, Guerrier G. The ascorbate-glutathione cycle in the cytosolic and chloroplastic fractions of drought-tolerant and drought-sensitive poplars. J Plant Physiol. 2001;158:1511– 1517.

Hajheidari M, Eivazi A, Buchanan BB, Wong JH, Majidi I, et al. Proteomics uncovers a role for redox in drought tolerance in wheat. J Proteome Res. 2007;6:1451– 1460. PubMed

Trachsel H, Staehelin T. Initiation of Mammalian Protein-Synthesis - Multiple Functions of the Initiation-Factor Eif-3. Biochim Biophys Acta. 1979;565:305– 314. PubMed

Peters HI, Chang YWE, Traugh JA. Phosphorylation of Elongation-Factor 1(Ef-1) by Protein-Kinase-C Stimulates Gdp/Gtp-Exchange Activity. Eur J Biochem. 1995;234:550– 556. PubMed

Oliver MJ, Jain R, Balbuena TS, Agrawal G, Gasulla F, et al. Proteome analysis of leaves of the desiccation-tolerant grass, Sporobolus stapfianus, in response to dehydration. Phytochemistry. 2011;72:1273– 1284. PubMed

Yang F, Wang Y, Miao LF. Comparative physiological and proteomic responses to drought stress in two poplar species originating from different altitudes. Physiol Plant. 2010;139:388– 400. PubMed

Pinheiro C, Kehr J, Ricardo CP. Effect of water stress on lupin stem protein analysed by two-dimensional gel electrophoresis. Planta. 2005;221:716– 728. PubMed

Wu WW, Wang GH, Baek SJ, Shen RF. Comparative study of three proteomic quantitative methods, DIGE, cICAT, and iTRAQ, using 2D gel- or LC-MALDI TOF/TOF. J Proteome Res. 2006;5:651– 658. PubMed

Alvarez S, Berla BM, Sheffield J, Cahoon RE, Jez JM, et al. Comprehensive analysis of the Brassica juncea root proteome in response to cadmium exposure by complementary proteomic approaches. Proteomics. 2009;9:2419– 2431. PubMed

Mechin V, Balliau T, Chateau-Joubert S, Davanture M, Langella O, et al. A two-dimensional proteome map of maize endosperm. Phytochemistry. 2004;65:1609– 1618. PubMed

Vincent D, Ergul A, Bohlman MC, Tattersall EAR, Tillett RL, et al. Proteomic analysis reveals differences between Vitis vinifera L. cv. Chardonnay and cv. Cabernet Sauvignon and their responses to water deficit and salinity. J Exp Bot. 2007;58:1873– 1892. PubMed

Fischer RA, Maurer R. Drought resistance in spring wheat cultivars. I. Grain yield responses. Austr J Agric Res. 1978;29:897– 917.

Rosielle AA, Hamblin J. Theoretical aspects of selection for yield in stress and non-stress environments. Crop Sci. 1981;21:943– 946.

Hola D, Kocova M, Rothova O, Wilhelmova N, Benesova M. Recovery of maize (Zea mays L.) inbreds and hybrids from chilling stress of various duration: Photosynthesis and antioxidant enzymes. J Plant Physiol. 2007;164:868– 877. PubMed

Nakano Y, Asada K. Hydrogen-Peroxide Is Scavenged by Ascorbate-Specific Peroxidase in Spinach-Chloroplasts. Plant Cell Physiol. 1981;22:867– 880.

Smith IK, Vierheller TL, Thorne CA. Assay of Glutathione-Reductase in Crude Tissue-Homogenates Using 5,5′-Dithiobis(2-Nitrobenzoic Acid). Anal Biochem. 1988;175:408– 413. PubMed

Ukeda H, Maeda S, Ishii T, Sawamura M. Spectrophotometric assay for superoxide dismutase based on tetrazolium salt 3′-{1-[(phenylamino)-carbonyl]-3,4-tetrazolium}-bis(4-methoxy-6-nitro)benzenesulfonic acid hydrate reduction by xanthine-xanthine oxidase. Anal Biochem. 1997;251:206– 209. PubMed

Thomas DJ, Avenson TJ, Thomas JB, Herbert SK. A cyanobacterium lacking iron superoxide dismutase is sensitized to oxidative stress induced with methyl viologen but is not sensitized to oxidative stress induced with norflurazon. Plant Physiol. 1998;116:1593– 1602. PubMed PMC

Bradford MM. Rapid and Sensitive Method for Quantitation of Microgram Quantities of Protein Utilizing Principle of Protein-Dye Binding. Anal Biochem. 1976;72:248– 254. PubMed

Gorg A, Obermaier C, Boguth G, Harder A, Scheibe B, et al. The current state of two-dimensional electrophoresis with immobilized pH gradients. Electrophoresis. 2000;21:1037– 1053. PubMed

Blum H, Beier H, Gross HJ. Improved Silver Staining of Plant-Proteins, Rna and Dna in Polyacrylamide Gels. Electrophoresis. 1987;8:93– 99.

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