Department of Crop Science, Chungbuk National University, 410 Seongbong-ro, Heungdeok-gu, Cheongju, Chungbuk, 361-763, Korea.
Mol Biol Rep. 2012 May;39(5):5069-83. doi: 10.1007/s11033-011-1302-4. Epub 2011 Dec 11.
We utilized Percoll density gradient centrifugation to isolate and fractionate chloroplasts of Korean winter wheat cultivar cv. Kumgang (Triticum aestivum L.). The resulting protein fractions were separated by one dimensional polyacrylamide gel electrophoresis (1D-PAGE) coupled with LTQ-FTICR mass spectrometry. This enabled us to detect and identify 767 unique proteins. Our findings represent the most comprehensive exploration of a proteome to date. Based on annotation information from the UniProtKB/Swiss-Prot database and our analyses via WoLF PSORT and PSORT, these proteins are localized in the chloroplast (607 proteins), chloroplast stroma (145), thylakoid membrane (342), lumens (163), and integral membranes (166). In all, 67% were confirmed as chloroplast thylakoid proteins. Although nearly complete protein coverage (89% proteins) has been accomplished for the key chloroplast pathways in wheat, such as for photosynthesis, many other proteins are involved in regulating carbon metabolism. The identified proteins were assigned to 103 functional categories according to a classification system developed by the iProClass database and provided through Protein Information Resources. Those functions include electron transport, energy, cellular organization and biogenesis, transport, stress responses, and other metabolic processes. Whereas most of these proteins are associated with known complexes and metabolic pathways, about 13% of the proteins have unknown functions. The chloroplast proteome contains many proteins that are localized to the thylakoids but as yet have no known function. We propose that some of these familiar proteins participate in the photosynthetic pathway. Thus, our new and comprehensive protein profile may provide clues for better understanding that photosynthetic process in wheat.
我们利用聚蔗糖(Percoll)密度梯度离心法从韩国冬小麦品种 Kumgang(普通小麦)中分离和分级叶绿体。所得蛋白质组分通过一维聚丙烯酰胺凝胶电泳(1D-PAGE)与 LTQ-FTICR 质谱法分离。这使我们能够检测和鉴定 767 种独特的蛋白质。我们的研究结果代表了迄今为止对蛋白质组进行的最全面的探索。基于 UniProtKB/Swiss-Prot 数据库的注释信息以及我们通过 WoLF PSORT 和 PSORT 的分析,这些蛋白质定位于叶绿体(607 种蛋白质)、叶绿体基质(145 种)、类囊体膜(342 种)、腔(163 种)和整合膜(166 种)。所有这些中,有 67%被证实为叶绿体类囊体蛋白。尽管已经完成了小麦中关键叶绿体途径(如光合作用)的几乎完整的蛋白质覆盖(89%的蛋白质),但许多其他蛋白质参与了碳代谢的调节。根据 iProClass 数据库开发的分类系统和通过 Protein Information Resources 提供的分类系统,鉴定出的蛋白质被分配到 103 个功能类别。这些功能包括电子传递、能量、细胞组织和生物发生、运输、应激反应和其他代谢过程。虽然这些蛋白质中的大多数与已知的复合物和代谢途径有关,但约 13%的蛋白质具有未知的功能。叶绿体蛋白质组包含许多定位于类囊体但尚未具有已知功能的蛋白质。我们推测其中一些熟悉的蛋白质参与光合作用途径。因此,我们新的和全面的蛋白质图谱可能为更好地理解小麦中的光合作用过程提供线索。