ISOLATION OF A TENFOLD HIS-TAGGED D1 PROTEIN FROM CHLAMYDOMONAS REINHARDTII USING NI-NTA AGAROSE

Автор(и)

  • Ilka HÄNßGEN Scil Proteins GmbH, Німеччина

Ключові слова:

Chlamydomonas reinhardtii, білок D1, фотосистема II, His-tag

Анотація

Щоб зробити білок D1 доступним для дослідження та аналізу змін, чистий препарат D1, який здійснює накопичення білка D1 швидким та відтворювальним методом, є необхідним. Дана робота представляє цей метод. Внутрішня структура білка D1 chlorophycee Chlamydomonas reinhardtii була включена в цикл D-e. Після зв’язування рідної, солюбілізованої фотосистеми ІІ (ФС) для Ni-NTA агарози білка D1 зібрані компоненти були змиті за допомогою 8 М мочевини та 0,3 % SDS. Ізольовані білки D1 можна виявити за допомогою фарбування в Кумассі після SDS-PAGE. Вимивається білок D1, який міститься у вигляді домішки тільки білка D2, який був зв’язаний з D1. Використання перекису водню показали, що очищений білок D1 може бути використаний для обмеження аналізу в пробірці. Обмежені фрагменти легко виявити на срібному забарвленні – замість реакції антитіл.

Біографія автора

Ilka HÄNßGEN, Scil Proteins GmbH

Scientist Protein Analytics

Посилання

Allakhverdiev SI, Murata N (2004) Environmental stress inhibits the synthesis de novo of proteins involved in the photodamage-repair

cycle of Photosystem II in Synechocystis sp. PCC 6803. Biochim Biophys Acta 1657:23-32.

Arnon DI (1949) Copper Enzymes in Isolated Chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiol 24:1-15.

Aro EM, Virgin I, Andersson B (1993) Photoinhibition of Photosystem II. Inactivation, protein damage and turnover. Biochim Biophys Acta 1143:113-134.

Berkelman T, Stenstedt T (1998) 2-D Electrophoresis using immobilized pH gradients principles & methods. Amersham Pharmacia

Biotech Inc.

Berthold DA, Babcock GT, Yocum CF (1981) A highly resolved, oxygen-evolving photosystem II preparation from spinach thylakoid

membranes. FEBS lett 134 (2):231-234.

Cullen M, Ray N, Husain S, Nugent J, Nield J, Purton S (2007) A highly active histidine-tagged Chlamydomonas reinhardtii

Photosystem II preparation for structural and biophysical analysis. Photochem Photobiol Sci 6:1177-1183

Dauvillee D, Hilbig L, Preiss S, Johanningmeier U (2004) Minimal Extent of Sequence Homology Required for Homologous Recombination at the psbA Locus in Chlamydomonas reinhardtii Chloroplasts using PCR-generated DNA Fragments. Photosynth Res 79:219-224.

Diner BA, Wollman FA (1980) Isolation of highly active photosystem II particles from a mutant of Chlamydomonas reinhardtii. Eur J Biochem 110:521-526.

Gorman DS, Levine RP (1965) Cytochrome f and plastocyanin: their sequence in the photosynthetic electron transport chain of

Chlamydomonas reinhardii. Proc Natl Acad Sci U S A 54:1665-1669.

Hanahan D (1983) Studies on transformation of Escherichia coli with plasmids. J Mol Biol 166:557-580.

Herbert B (1999) Advances in protein solubilisation for two-dimensional electrophoresis. Electrophoresis 20:660-663.

Ishikawa Y, Nakatani E, Henmi T, Ferjani A, Harada Y, Tamura N, Yamamoto Y (1999) Turnover of the aggregates and cross-linked

products of the D1 protein generated by acceptor-side photoinhibition of photosystem II. Biochim Biophys Acta 1413:147-158.

Klein TM, Wolf ED, Sanford JC (1987) High-velocity microprojectiles for delivering nucleic acids into living cells. Nature 327:70-73.

Kless H, Vermaas W (1995). Tandem sequence duplications functionally complement deletions in the D1 protein of photosystem II. J Biol Chem 270(28):16536-41.

Kroczek RA (1993). Southern and northern analysis. J Chromatogr 618, 133-145.

Kuwabara T, Murata N (1982). Inactivation of photosynthetic oxygen evolution and concomitant release of three polypeptides in the photosystem II particles of spinach chloroplasts. Plant Cell Physiol 23:533-539.

Laemmli UK (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227(5259):680-5.

Lucinski R, Jackowski G (2006) The structure, functions and degradation of pigment-binding proteins of photosystem II. Acta Biochim Pol 53:693-708.

Lupinkova L, Komenda J (2004). Oxidative modifications of the Photosystem II D1 protein by reactive oxygen species: from isolated

protein to cyanobacterial cells. Photochem Photobiol 79:152-162.

Merril CR (1990). Gel-staining techniques. Methods Enzymol 182:477-488.

Miyao M (1994). Involvement of active oxygen species in degradation of the D1 protein under strong illumination in isolated subcomplexes of photosystem II. Biochemistry 33:9722-9730.

Nanba O, Satoh K (1987). Isolation of a photosystem II reaction center consisting of D-1 and D-2 polypeptides and cytochrome b-559.

Proc Natl Acad Sci U S A 84:109-112.

Nixon PJ, Komenda J, Barber J, Deak Z, Vass I, Diner BA (1995). Deletion of the PEST-like region of photosystem two modifies the

QB-binding pocket but does not prevent rapid turnover of D1. J Biol Chem 270:14919-14927.

Preiss S, Schrader S, Johanningmeier U (2001). Rapid, ATP-dependent degradation of a truncated D1 protein in the chloroplast. Eur J Biochem 268:4562-4569.

Robinson HH, Sharp RR, Yocum CF (1980). Effect of manganese on the nuclear magnetic relaxivity of water protons in chloroplast

suspensions. Biochem Biophys Res Commun 93:755-761.

Sambrook J, Fritsch EF, Maniatis T (1989) Molecular Cloning: a Laboratory Manual. 2nd Ed., Cold Spring Harbor Laboratory press,

New York.

Schägger H, Borchart U, Aquila H, Link TA, von Jagow G (1985). Isolation and amino acid sequence of the smallest subunit of beef

heart bc1 complex. FEBS Lett 190:89-94.

Schiller H, Dau H (2000). Preparation protocols for high-activity photosystem II membrane particles of green algae and higher plants,

pH dependence of oxygen evolution and comparison of the S2-state multiline signal by X-band EPR spectroscopy. J Photochem

Photobiol B 55:138-144.

Shim H, Cao J, Govindjee, Debrunner PG (1990) Purification of highly active oxygen-evolving photosystem II from Chlamydomonas

reinhardtii. Photos Res 26:223-228.

Shipton CA, Barber J (1991). Photoinduced degradation of the D1 polypeptide in isolated reaction centers of photosystem II: evidence

for an autoproteolytic process triggered by the oxidizing side of the photosystem. Proc Natl Acad Sci U S A 88:6691-6695.

Shneyour A, Avron M (1970). High biological activity in chloroplasts from Euglena gracilis prepared with a new gas pressure device.

FEBS Lett 8:164-166.

Sueoka N (1960). Mitotic replication of deoxyribonucleic acid in Chlamydomonas reinhardtii. Proc Natl Acad Sci. U S A 46:83-91.

Sugiura M, Inoue Y, Minagawa J (1998). Rapid and discrete isolation of oxygen-evolving His-tagged photosystem II core complex

from Chlamydomonas reinhardtii by Ni2+ affinity column chromatography. FEBS Lett 426:140-144.

Sugiura M, Inoue Y (1999). Highly purified thermo-stable oxygen-evolving photosystem II core complex from the thermophilic

cyanobacterium Synechococcus elongatus having His-tagged CP43. Plant Cell Physiol 40:1219-1231.

Suzuki T, Minagawa J, Tomo T, Sonoike K, Ohta H, Enami I (2003). Binding and functional properties of the extrinsic proteins in oxygenevolving photosystem II particle from a green alga, Chlamydomonas reinhardtii having his-tagged CP47. Plant Cell Physiol 44:76-84.

Takahashi Y, Utsumi K, Yamamoto Y, Hatano A, Satoh K (1996). Genetic engineering of the processing site of D1 precursor protein

of photosystem II reaction center in Chlamydomonas reinhardtii. Plant Cell Physiol 37(2):161-8.

Tang XS, Fushimi K, Satoh K (1990). D1-D2 complex of the photosystem II reaction center from spinach. Isolation and partial

characterization. FEBS Lett 273:257-260.

Torreilles J, Guerin MC, Slaoui-Hasnaoui A (1990). Nickel (II) complexes of histidyl-peptides as Fenton-reaction catalysts. Free Radic Res Commun 11:159-166.

Towbin H, Staehelin T, Gordon J (1979). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets:

procedure and some applications. Proc Natl Acad Sci U S A 76:4350-4354.

##submission.downloads##

Номер

Розділ

МЕТОДИЧНІ ПИТАННЯ ЕКОЛОГІЇ