Irrgang K D, Shi L X, Funk C, Schröder W P
Department of Biochemistry, Arrhenius Laboratories for Natural Sciences, Stockholm University, Sweden.
J Biol Chem. 1995 Jul 21;270(29):17588-93. doi: 10.1074/jbc.270.29.17588.
A nuclear-encoded polypeptide of 6.1 kDa was identified in isolated photosystem II (PSII) reaction center from Spinacia oleracea. The hydrophobic membrane protein easily escapes staining procedures such as Coomassie R-250 or silver staining, but it is clearly detected by immunodecoration with peptide-directed IgG. This additional subunit was found to be present in PSII reaction centers previously known to contain only the D1/D2/cytb559 proteins and the psbI gene product. Furthermore, cross-linking experiments using 1-(3-dimethylaminopropyl-) 3-ethylcarbodiimide showed that the nearest neighbors were the D1 and D2 proteins and the cytb559. The 6.1-kDa protein was purified by immune affinity chromatography. N-terminal sequence analysis of the isolated protein confirmed the identity of the 6.1-kDa protein and enabled finding of strong similarities with a randomly obtained cDNA from Arabidopsis thaliana. Using enzyme-linked immunosorbent assay in combination with thylakoid membrane preparations of different orientation, the N terminus of the protein, predicted to span the membrane once, is suggested to be exposed at the lumen side of the membrane. Consequently the 6.1-kDa protein seems to be the only subunit in the PSII reaction center that is nuclear encoded and has its N terminus on the lumen side of the membrane. These findings open for new interesting suggestions concerning the properties of photosystem II reaction center with respect to the photosynthetic activity, regulation and assembly in higher plants.
在从菠菜中分离出的光系统II(PSII)反应中心中鉴定出一种6.1 kDa的核编码多肽。这种疏水膜蛋白很容易逃过考马斯亮蓝R-250或银染等染色程序,但通过肽导向的IgG进行免疫印迹可清晰检测到。发现这个额外的亚基存在于之前已知仅包含D1/D2/cytb559蛋白和psbI基因产物的PSII反应中心中。此外,使用1-(3-二甲基氨基丙基)-3-乙基碳二亚胺进行的交联实验表明,其紧邻的蛋白是D1、D2蛋白和cytb559。通过免疫亲和层析纯化了6.1 kDa的蛋白。对分离出的蛋白进行N端序列分析,确认了6.1 kDa蛋白的身份,并发现它与从拟南芥中随机获得的cDNA有很强的相似性。结合不同取向的类囊体膜制剂进行酶联免疫吸附测定,预计该蛋白的N端跨膜一次,且暴露于膜的腔侧。因此,6.1 kDa蛋白似乎是PSII反应中心中唯一由核编码且N端位于膜腔侧的亚基。这些发现为关于高等植物光系统II反应中心在光合活性、调节和组装方面的特性提出了新的有趣见解。