Anti-PsbE | Alfa subunit of Cytochrome b559 of PSII

Chlamydomonas reinhardtii, diatoms, Synechococcus sp. PCC 7942

2 µg of total protein from (1) Arabidopsis thaliana leaf, (2) Horderum vulgare leaf ), (3) Chlamydomonas reinhardtii total cell , (4) Synechococcus sp. 7942 total cell were all extracted with Agrisera Protein Extraction Buffer (AS08 300) and separated on 4-12% NuPage (Invitrogen) LDS-PAGE and blotted 1h to PVDF. Blots were blocked immediately following transfer in 2% blocking reagent in 20 mM Tris, 137 mM sodium chloride pH 7.6 with 0.1% (v/v) Tween-20 (TBS-T) for 1h at room temperature with agitation. Blots were incubated with the primary antibody at a dilution of 1: 10 000 for 1h at room temperature with agitation. The antibody solution was decanted and the blot was rinsed briefly twice, then washed once for 15 min and 3 times for 5 min in TBS-T at RT with agitation. Blots were incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated) diluted to 1:50 000 in 2% blocking solution for 1h/RT with agitation. The blots were washed as above and developed for 5 min with chemiluminescent detection reagent of extreme femtogram range, according to the manufacturers instructions. Images of the blots were obtained using a CCD imager (FluorSMax, Bio-Rad) and Quantity One software (Bio-Rad). Exposure time was 1 second.

The detection of PsbE proteins was performed using isolated thylakoids from Arabidopsis thaliana and Oryza sativa. Fresh leaf samples (≈ 10 g), 30 min-dark acclimated, were washed and ground in a blender with ice-cold grinding buffer (20 mM Tricine (pH 8.4), containing 0.4 M sorbitol, 5 mM EDTA, 10 mM NaHCO₃ and 0.5% BSA). The homogenate was double filtered with two layers of musseline and centrifugated at 4,000 x g for 10 min (4°C). The supernatant was discarded and the pellet was resuspended in an ice-cold resuspending buffer (20 mM Hepes, pH 7.6, 0.3 M sorbitol, 2.5 mM EDTA, 10 mM NaHCO₃ and 0.5% BSA). The solution was centrifugated at 4,000 x g for 10 min (4°C), the supernatant was discarded and the pellet was resuspended in a hypotonic buffer (20 mM Hepes, pH 7.6, 2.5 mM EDTA, 10 mM NaHCO₃ and 0.5% BSA). The solution was centrifugated (4,000 x g for 10 min, 4°C), the supernatant was discarded and the pellet was resuspended in 1 mL of resuspending buffer. Subsequently, total chlorophyll concentration was determined according to Porra et al. (1989). For the western blot, thylakoid protein extracts were first separated by SDS-PAGE (Laemmli, 1970). Equal volumes (10 mL) of sample containing 4, 2 and 1 µg Chl were electrophoretically transferred to a nitrocellulose membrane (Towbin et al., 1979). Polypeptide detection was performed using specific polyclonal antibodies, anti-PsbE (AS06 112 - AgriserA). Membranes were blocked for 3 hours with 5% non-fat milk in saline Tris-HCl buffer (100 mM Tris-HCl, pH 7.6, 150 mM NaCl), incubated with PsbE antibody overnight and after with HRP-conjugated secondary antibody (AS09 602) by 3 hours. The protein detection was developed using 100 Mm Tris-HCl buffer (pH 7.2) containing 100 mg/mL DAB, 400 mg/mL NiCl₂ and 0.04% H₂O₂, until bands were visualized.

Courtesy of Dr. Ana Karla Moreira Lobo, Laboratory of Plant Metabolism, Federal University of Ceara - Brazil

Cytochrome b559 (Cyt b559) is encoded by the chloroplast genes psbE and psbF and is comprised of two low molecular mass polypeptides, a and h subunits, with molecular masses of 9 and 4 kDa, respectively. The Cyt b559 is closely associated with PSII in all oxygenic photosynthetic organisms. The a and h subunits of the Cyt b559 are components of the minimal PSII reaction center complex that is still capable of primary charge separation In summary, both PsbE and PsbF are essential components for PSII assembly, and they are probably involved in electron transport mechanisms that help to protect PSII from photodamage.
Alternative protein name: PSII reaction center subunit V