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藓类植物小立碗藓(Physcomitrella patens (Hedw.) B.S.G.)的蛋白质组分析

Proteome analysis of the moss Physcomitrella patens (Hedw.) B.S.G.

作者信息

Skripnikov A Yu, Polyakov N B, Tolcheva E V, Velikodvorskaya V V, Dolgov S V, Demina I A, Rogova M A, Govorun V M

机构信息

Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, 117997, Russia.

出版信息

Biochemistry (Mosc). 2009 May;74(5):480-90. doi: 10.1134/s0006297909050022.

Abstract

The sequencing of the moss Physcomitrella patens genome has facilitated studies of the plant proteome. To develop a proteome reference map based on the genome sequence, we conducted 2D electrophoreses of proteins extracted from moss protoplasts, protonemata, and gametophores grown under standard conditions on Petri dishes. On silver-stained gels, depending on the developmental stage of the moss, we resolved from 500 to 600 protein spots that were then excised and digested by trypsin, and 212 proteins were identified by PMF-MALDI-TOF. To enhance the proteome coverage, we performed 1D SDS-PAGE with subsequent separation of tryptic peptides derived from digested gel band slices by LC-ESI-MS/MS. The proposed approach allowed us to identify 186 proteins had not been determined by 2D PMF-MALDI-TOF. Proteins identified by both methods were categorized using a system of clusterization of orthologous genes as metabolism (26%), cellular processes and signaling (16%), and information storage and processing (7%). Proteome analysis by differential gel electrophoresis revealed moderate differences between filamentous protonemata and leafy shoots. Surprisingly, protoplasts isolated from protonema filaments displayed significant differences in protein composition compared with both protonemata and gametophores.

摘要

小立碗藓(Physcomitrella patens)基因组的测序推动了对植物蛋白质组的研究。为了基于基因组序列绘制蛋白质组参考图谱,我们对在培养皿中标准条件下生长的藓类原生质体、原丝体和配子体中提取的蛋白质进行了二维电泳。在银染凝胶上,根据藓类的发育阶段,我们分辨出500至600个蛋白质点,随后将其切除并用胰蛋白酶消化,通过PMF-MALDI-TOF鉴定出212种蛋白质。为了提高蛋白质组覆盖率,我们进行了一维SDS-PAGE,随后通过LC-ESI-MS/MS对消化后的凝胶条切片衍生的胰蛋白酶肽进行分离。所提出的方法使我们能够鉴定出186种通过二维PMF-MALDI-TOF未确定的蛋白质。通过两种方法鉴定的蛋白质使用直系同源基因聚类系统进行分类,分为代谢(26%)、细胞过程和信号传导(16%)以及信息存储和处理(7%)。差异凝胶电泳分析蛋白质组揭示了丝状原丝体和叶状茎之间存在适度差异。令人惊讶的是,与原丝体和配子体相比,从原丝体细丝中分离出的原生质体在蛋白质组成上显示出显著差异。

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