期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
Strawberry vein banding virus P6 protein intracellular transport and an important domain identification
1
作者 PAN Yuan ZHOU Xiu-hong +8 位作者 LI Shuai FENG Ming-feng SHI Man-ling zuo deng-pan JIANG Xi-zi CHEN Jing HU Ya-hui ZHANG Xiang-xiang JIANG Tong 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2018年第9期2031-2041,共11页
Strawberry vein banding virus (SVBV)-infected strawberry cells contain cytoplasmic inclusions with isometric particles. To identify the components of the inclusions, green fluorescent protein (GFP) was fused to th... Strawberry vein banding virus (SVBV)-infected strawberry cells contain cytoplasmic inclusions with isometric particles. To identify the components of the inclusions, green fluorescent protein (GFP) was fused to the carboxy-terminus (C-terminus) of SVBV open reading frames, these constructs were separately transformed into Agrobacterium tumefaciens and infiltrated into Nicotiana benthamiana leaves. Results showed that the SVBV P6 protein assembled into prominent and amorphous inclusion bodies (IBs). To investigate P6 subcellular localization, P6-GFP was ectopically expressed in N. benthamiana leaves by agroinfiltration and then stained with 4",6-diamidino-2-phenylindole (DAPI). We found the P6 protein accumulated in the nuclei and also formed cytoplasmic IBs with different sizes. To further determine the location of P6 IBs in the cytoplasm, and explore whether the P6 IBs move freely or depend on cytoskeleton and endoplasmic reticulum (ER), the microfilament marker protein (GFP-ABD2-GFP), microtubules marker protein (mCherry-MAP65-1) and ER marker protein (mCherry-HDEL) were separately coexpressed with P6-GFP and into N. benthamiana leaves by agroinfiltration, exhibiting that P6 IBs aligned with cytoskeleton and endoplasmic reticulum. Meanwhile, coinfiltration of P1 and P6 indicated the P6 colocalized with the P1 protein at periphery of cells. The P6 protein contains one C-terminal nuclear localization signal (NLS) region, a P6 protein mutant with a deleted NLS did not localize in the nucleus, did not form IBs, and was unable to facilitate exogenous GFP expression. These results demonstrate that the deleted NLS region is an important P6 domain required for biological functions. In summary, the mobile P6 IBs are associated with ER, microfilaments and microtubules and move along microfilaments to the SVBV P1 protein in the PD. 展开更多
关键词 SVBV IBS intracellular transport CYTOSKELETON ER P6 mutant
下载PDF
大麦黄矮病毒PAV青海分离物运动蛋白抗血清制备及其与同属BYDVs的血清学关系 被引量:3
2
作者 胡汝检 赵添羽 +3 位作者 左登攀 王颖 张宗英 韩成贵 《植物病理学报》 CAS CSCD 北大核心 2020年第2期141-146,共6页
大麦黄矮病毒(Barley yellow dwarf viruses, BYDVs)属于黄症病毒科,主要以蚜虫为介体进行传播,引发多种作物减产或绝收。本文将BYDV-PAV青海分离物的运动蛋白(MP)克隆到原核表达载体pDB-MBP-His上,转化大肠杆菌Rosetta(DE3),在IPTG诱... 大麦黄矮病毒(Barley yellow dwarf viruses, BYDVs)属于黄症病毒科,主要以蚜虫为介体进行传播,引发多种作物减产或绝收。本文将BYDV-PAV青海分离物的运动蛋白(MP)克隆到原核表达载体pDB-MBP-His上,转化大肠杆菌Rosetta(DE3),在IPTG诱导下表达蛋白分子量约为61 kDa的融合蛋白。将纯化后的蛋白作为抗原免疫‘新西兰’大白兔制备抗血清,Western blot检测本生烟瞬时表达带标签的MP蛋白,结果显示该抗血清效价为1∶32 000,灵敏度达1∶256,且该抗血清可与相差34个氨基酸的PAV015株系以及隶属于黄症病毒属其他的BYDVs(PAS、MAV、KerⅡ和KerⅢ)MP均能发生强烈的血清学反应,具有血清学相关性。本研究制备的大麦黄矮病毒PAV青海分离物运动蛋白多克隆抗体为探索BYDV-PAV运动蛋白的功能以及作用机制打下了基础。 展开更多
关键词 大麦黄矮病毒PAV 运动蛋白 原核表达 抗血清制备 血清学关系
原文传递
甘蔗黄叶病毒运动蛋白的原核表达和抗血清制备 被引量:2
3
作者 刘玉姿 张绍康 +5 位作者 田畅 张晓艳 左登攀 王颖 张宗英 韩成贵 《植物病理学报》 CAS CSCD 北大核心 2020年第6期694-701,共8页
甘蔗黄叶病毒(Sugarcane yellow leaf virus,ScYLV)属于黄症病毒科(Luteoviridae)、马铃薯卷叶病毒属(Polerovirus),主要由蚜虫传播,能够侵染甘蔗、玉米等多种作物,引发严重的植物病害。本研究将编码ScYLV运动蛋白(Movement protein,MP... 甘蔗黄叶病毒(Sugarcane yellow leaf virus,ScYLV)属于黄症病毒科(Luteoviridae)、马铃薯卷叶病毒属(Polerovirus),主要由蚜虫传播,能够侵染甘蔗、玉米等多种作物,引发严重的植物病害。本研究将编码ScYLV运动蛋白(Movement protein,MP)的基因连接到pDB-His-MBP原核表达载体上,转化到大肠杆菌菌株Rosetta中,经IPTG诱导,表达分子量大小约为70 kDa的融合蛋白,将纯化后的融合蛋白制备多克隆抗血清。利用western blot检测抗血清的效价为1∶128000,灵敏度为1∶256,抗血清不与马铃薯卷叶病毒属(Polerovirus)的其它病毒以及黄症病毒属(Luteovirus)病毒发生交叉反应,具有很好的特异性。本文制备的ScYLV MP抗血清可以用于ScYLV的检测,并为深入研究ScYLV与寄主的相互作用等问题提供材料基础。 展开更多
关键词 甘蔗黄叶病毒 运动蛋白 原核表达 瞬时表达 抗血清
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部