Name: modifying baculovirus expression vectors to produce secreted plant proteins in insect cells
Uploaded: 2018-08-20T15:00:00
Description: Watch this Scientific Journal Video about Modifying Baculovirus Expression Vectors to Produce Secreted Plant Proteins in Insect Cells at JoVE.com

这项工作得到了来自北卡罗来纳州立大学 Guozhou 许的新的教员启动基金的支持。

注: 采用修饰表达载体的昆虫细胞/杆状病毒系统, 用于分泌植物蛋白的表达和结晶。
1. 用 GP67 信号肽对杆状病毒表达载体进行植物蛋白分泌表达的改进
<ol><li>合成一个 DNA 片段, 包含 5 ' BglII 切割站点13, GP67 分泌信号序列, 和一个多克隆网站与 NotI, BamHI, EcoRI, StuI, 贝里沙, SpeI, XbaI, PstI 和 XhoI (图 1A)。 注: 由于 BglII 和 BamHI 消化 dna 导致?...

<ol>
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鉴于生物系统中数以千计的蛋白质的大小和稳定性的多样性, 研究实验室通常有经验来决定哪些异种表达系统必须选择用于表达特定的蛋白质。大肠杆菌表达系统往往是由于细菌生命周期短、培养基成本低、相对容易扩展19而导致蛋白质表达的首选。然而, 对于大小超过 60 kDa 的大真核蛋白的表达, 使用大肠杆菌系统往往导致不溶性蛋白在包涵体或聚集20<...

研究实验室有能力生产大量的均质重组蛋白, 用于生化和生物物理特征, 尤其是 x 射线晶体学研究。大肠杆菌、酵母、昆虫细胞、哺乳动物细胞、植物细胞等具有良好的外源表达系统, 其中杆状病毒介导的昆虫细胞表达系统是其中最常用的技术生产大量的结构折叠大型重组真核蛋白的蛋白质结晶1。
对杆状病毒表达系统的表达载体进行了设计, 以包含强多角体或 P10 启动子, 以产生高产量的重组细胞内蛋白2,3。为了制作重组杆状病毒, 该基因被克隆成含有杆状使用杆状多 nucleopolyhedroviral 基因组多角体 (polh) 轨迹的昆虫载体。然后对生成的构造进行排序, 验证其正确的开放阅读框架 (ORF)。通过转染过程将正确的构造引入宿主昆虫细胞。兴趣基因通过同源重组插入病毒基因组。这一事件导致重组病毒基因组的生产, 然后复制, 以产生重组发芽病毒粒子1。
在表达系统中最常用的昆虫细胞是 Sf9 和高五 (Hi5) 细胞。Sf9 细胞是 Sf21 蛹卵巢细胞的克隆分离物, Hi5 细胞是由父母夜蛾镍卵巢细胞系 TN-3684,5所衍生的克隆分离株。transfections、病毒扩增和斑块检测是在 Sf9 细胞上进行的, 而 Hi5 细胞通常被选择以产生更高数量的重组蛋白6。值得注意的是, Hi5 细胞由于其产生突变病毒的倾向而不适合于病毒后代的产生和扩增。传统上, 25-30 °c 的温度范围被认为对昆虫细胞的培养是有益的。然而, 据报道, 27-28 °c 是最佳的温度为昆虫细胞生长和传染7,8。
在基因之前引入一个强烈的信号序列是分泌蛋白的高表达所必需的。该信号序列将有效地引导转化后的重组蛋白转化为内质网的蛋白质分泌和转化后的修改必要的适当折叠和稳定3。信号肽序列, 如杆状病毒包络蛋白 GP64/67, 蜜蜂蜂毒等, 已被选择, 以促进分泌重组蛋白的表达在杆状病毒介导的表达系统3。GP67 的信号肽的引入, 以提高分泌重组蛋白的表达率, 与使用目标基因9的内在信号肽相比较。Hemolin 是大丝蛾Hyalophora cecropia的血淋巴蛋白, 引起细菌感染10。由于诱导表达水平较高, 该基因的信号肽序列可以用来调节杆状病毒-昆虫细胞系统中重组蛋白的分泌表达。
Tracheary 元素分化抑制因子受体 (TDR) 和花粉受体激酶 3 (PRK3) 都属于植物亮氨酸丰富的重复受体样激酶 (LRR RLK) 蛋白11,12 的家庭.为了研究植物受体蛋白家族的结构和功能, 以及促进其他植物分泌蛋白的结构和生化特性, 对杆状病毒-昆虫细胞表达系统进行了改进, 以提高蛋白质质量和产量。利用两种修饰表达载体在杆状病毒-昆虫细胞表达系统中成功地表达了 TDR 和 PRK3 的胞外域。TDR 和 PRK3 蛋白的胞外域均已结晶。本文报道了两种改进的杆状病毒表达载体的大量重组分泌植物蛋白的表达和纯化, 通过在启动子和多克隆之间加入 GP67 或 hemolin 信号序列。网站。

<table>
	<tbody>
		<tr>
			<td>Incubator shaker</td>
			<td>VWR</td>
			<td>Model Excella E25</td>
			<td>27 oC</td>
		</tr>
		<tr>
			<td>Incubator</td>
			<td>VWR</td>
			<td>Model 2005</td>
			<td>27 oC</td>
		</tr>
		<tr>
			<td>Centrifuge</td>
			<td>BECKMAN</td>
			<td>Model J-6</td>
			<td>with a swing bucket rotor</td>
		</tr>
		<tr>
			<td>Herculase II Fusion DNA Polymerase</td>
			<td>Agilent</td>
			<td>600677-51</td>
			<td>For PCR amplification of DNA</td>
		</tr>
		<tr>
			<td>Thermal Cycler</td>
			<td>BIO-RAD</td>
			<td>Model C1000 Touch</td>
			<td>For PCR amplification of DNA</td>
		</tr>
		<tr>
			<td>Incubator shaker</td>
			<td>New Brunswick Scientific</td>
			<td>Model I 24</td>
			<td>For growing baceria culture</td>
		</tr>
		<tr>
			<td>Customer DNA synthesis</td>
			<td>GENSCRIPT</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>BamHI (HF)</td>
			<td>New England Biolabs</td>
			<td>R3136S</td>
			<td>Restriction Endonuclease</td>
		</tr>
		<tr>
			<td>BglII</td>
			<td>New England Biolabs</td>
			<td>R0144S</td>
			<td>Restriction Endonuclease</td>
		</tr>
		<tr>
			<td>NotI (HF)</td>
			<td>New England Biolabs</td>
			<td>R3189S</td>
			<td>Restriction Endonuclease</td>
		</tr>
		<tr>
			<td>XhoI</td>
			<td>New England Biolabs</td>
			<td>R0146S</td>
			<td>Restriction Endonuclease</td>
		</tr>
		<tr>
			<td>T4 DNA ligase</td>
			<td>New England Biolabs</td>
			<td>M0202T</td>
			<td>DNA ligation</td>
		</tr>
		<tr>
			<td>QIAquick Gel Extraction Kit</td>
			<td>Qiagen</td>
			<td>28704</td>
			<td>DNA purification from Agorase gel</td>
		</tr>
		<tr>
			<td>QIAprep Spin Miniprep Kit</td>
			<td>Qiagen</td>
			<td>27104</td>
			<td>Plasmid DNA purification from bacteria culture</td>
		</tr>
		<tr>
			<td>Agarose</td>
			<td>Thermo Fisher Scientific</td>
			<td>15510-019</td>
			<td>For DNA gel electropherosis</td>
		</tr>
		<tr>
			<td>MAX Efficiency DH5&#945; competen cell</td>
			<td>Invitrogen</td>
			<td>18-258-012</td>
			<td>For transformation of DNA ligation mixture</td>
		</tr>
		<tr>
			<td>Lennox L LB Broth</td>
			<td>Research Product International Corp.</td>
			<td>L24066-5000.0</td>
			<td>For making bacteria culture</td>
		</tr>
		<tr>
			<td>Ampicillin sodium salt</td>
			<td>Thermo Fisher Scientific</td>
			<td>11593-019</td>
			<td>Antibiotics</td>
		</tr>
		<tr>
			<td>Kanamycin Sulfate</td>
			<td>Thermo Fisher Scientific</td>
			<td>15160-054</td>
			<td>Antibiotics</td>
		</tr>
		<tr>
			<td>Tetracycline</td>
			<td>Thermo Fisher Scientific</td>
			<td>64-75-5</td>
			<td>Antibiotics</td>
		</tr>
		<tr>
			<td>Gentamicin</td>
			<td>Thermo Fisher Scientific</td>
			<td>15710-064</td>
			<td>Antibiotics</td>
		</tr>
		<tr>
			<td>MAX Efficiency DH10Bac competent cells</td>
			<td>Thermo Fisher Scientific</td>
			<td>10361-012</td>
			<td>For making bacmid DNA</td>
		</tr>
		<tr>
			<td>S.O.C. Medium</td>
			<td>Thermo Fisher Scientific</td>
			<td>15544-034</td>
			<td>For DNA transformation</td>
		</tr>
		<tr>
			<td>CellFECTIN II Reagent</td>
			<td>Thermo Fisher Scientific</td>
			<td>10362-101</td>
			<td>Insect cell transfection reagent</td>
		</tr>
		<tr>
			<td>Bac-to-Bac Expression System</td>
			<td>Thermo Fisher Scientific</td>
			<td>10359-016</td>
			<td>Baculovirus-insect cells expression kit</td>
		</tr>
		<tr>
			<td>Bluo-gal</td>
			<td>Thermo Fisher Scientific</td>
			<td>15519-028</td>
			<td>For isolation of recominant Bacmid DNA</td>
		</tr>
		<tr>
			<td>IPTG</td>
			<td>Thermo Fisher Scientific</td>
			<td>15529-019</td>
			<td>For isolation of recominant Bacmid DNA</td>
		</tr>
		<tr>
			<td>pFastBac1</td>
			<td>Thermo Fisher Scientific</td>
			<td>10360014</td>
			<td>Baculorirus expression vector</td>
		</tr>
		<tr>
			<td>Sf9 cells</td>
			<td>Thermo Fisher Scientific</td>
			<td>11496015</td>
			<td>Sf9 monolayer cells</td>
		</tr>
		<tr>
			<td>Hi5 cells</td>
			<td>Thermo Fisher Scientific</td>
			<td>B85502</td>
			<td>High Five insect cells</td>
		</tr>
		<tr>
			<td>Grace&#8217;s insect medium, unsupplemented</td>
			<td>Thermo Fisher Scientific</td>
			<td>11595030</td>
			<td>Sf9 cell transfection minimum medium</td>
		</tr>
		<tr>
			<td>Grace&#8217;s insect medium, supplemented</td>
			<td>Thermo Fisher Scientific</td>
			<td>11605102</td>
			<td>Sf9 monolayer cell culture complete medium</td>
		</tr>
		<tr>
			<td>Sf-900 II SFM</td>
			<td>Thermo Fisher Scientific</td>
			<td>10902104</td>
			<td>Sf9 suspension cell culture medium without FBS</td>
		</tr>
		<tr>
			<td>Express Five SFM</td>
			<td>Thermo Fisher Scientific</td>
			<td>10486025</td>
			<td>Hi5 cell culture medium</td>
		</tr>
		<tr>
			<td>Penicillin-Streptomycin&#160;</td>
			<td>Thermo Fisher Scientific</td>
			<td>15140122</td>
			<td>100 ml (10,000 I.U./ml)</td>
		</tr>
		<tr>
			<td>L-Glutamine (200 mM)&#160;</td>
			<td>Thermo Fisher Scientific</td>
			<td>25030081</td>
			<td>100 ml</td>
		</tr>
		<tr>
			<td>FBS Certified</td>
			<td>Thermo Fisher Scientific</td>
			<td>16000-044</td>
			<td>500 ml</td>
		</tr>
		<tr>
			<td>6-well plates</td>
			<td>Thermo Fisher Scientific</td>
			<td>08-772-1B</td>
			<td>Flat-bottom</td>
		</tr>
		<tr>
			<td>150 mm plates</td>
			<td>Thermo Fisher Scientific</td>
			<td>353025</td>
			<td>100/case</td>
		</tr>
		<tr>
			<td>1.5 ml Microcentrifuge Tubes</td>
			<td>USA Scientific</td>
			<td>1415-2500</td>
			<td>500 tubes/bag</td>
		</tr>
		<tr>
			<td>15 ml conical screw cap centrifuge tubes</td>
			<td>USA Scientific</td>
			<td>1475-0511</td>
			<td>25 tubes/bag</td>
		</tr>
		<tr>
			<td>50 ml conical screw cap centrifuge tubes</td>
			<td>USA Scientific</td>
			<td>1500-1211</td>
			<td>25 tubes/bag</td>
		</tr>
		<tr>
			<td>Ni-NTA Superflow</td>
			<td>Qiagen</td>
			<td>30430</td>
			<td>NiNTA resin</td>
		</tr>
		<tr>
			<td>pH-indicator strips</td>
			<td>EMD Millipore Corporation</td>
			<td>1.09535.0001</td>
			<td>pH 0 - 14</td>
		</tr>
	</tbody>
</table>

modifying baculovirus expression vectors to produce secreted plant proteins in insect cells

对科学家来说, 表达重组分泌真核蛋白用于结构和生物化学研究是一个挑战。杆状病毒介导的昆虫细胞表达系统是用于表达重组真核分泌蛋白的系统之一, 具有一定的转化后修饰。分泌蛋白需要通过分泌通路进行蛋白质糖基化、二硫化键形成和其他转化后的修饰。为改善现有分泌植物蛋白的昆虫细胞表达, 在启动子和多克隆点之间添加 GP67 或 hemolin 信号肽序列, 对杆状病毒表达载体进行修改。新设计的改进后的载体系统成功地生产出了拟南芥可溶性重组分泌植物受体蛋白的高产。对两种表达的植物蛋白, 拟南芥和 PRK3 膜受体的胞外域进行了结晶, 用于 x 射线晶体的研究。改进后的矢量系统是一种改良的工具, 可用于动物王国中重组分泌蛋白的表达。

如图 1所示, 两种改进的 pFastBac1 杆状病毒表达载体用于表达 GP67 或 hemolin 信号序列的分泌蛋白, 以取代目标基因的内在信号序列。病毒 GP67 和昆虫 hemolin 基因已被证明具有较高的分泌表达水平的细胞。融合蛋白与这两个信号序列中的任何一个有望大大提高分泌表达水平。在这两种改进的向量中, 都设计了相同的多个克隆站点 (MCS)。NotI 站点被蓄意放置?...

Watch this Scientific Journal Video about Modifying Baculovirus Expression Vectors to Produce Secreted Plant Proteins in Insect Cells at JoVE.com

Modifying Baculovirus Expression Vectors to Produce Secreted Plant Proteins in Insect Cells

改进杆状病毒表达载体生产昆虫细胞分泌植物蛋白

在这里, 我们提出了利用昆虫细胞和杆状病毒蛋白表达系统来产生大量植物分泌蛋白的蛋白质结晶的协议。用 GP67 或昆虫 hemolin 信号肽对昆虫细胞中植物蛋白分泌表达进行了改进, 并对杆状病毒表达载体进行了修正。

It has been a challenge for scientists to express recombinant secretory eukaryotic proteins for structural and biochemical studies. The ...

Research

JoVE Journal

Biochemistry

Thermostabilization, Expression, Purification, and Crystallization of the Human Serotonin Transporter Bound to S-citalopram

Thermostabilization, Expression, Purification, and Crystallization of the Human Serotonin Transporter Bound to S-citalopram

热稳定，表达，纯化，和人类血清素转运蛋白结晶绑定到<em&gt;取值</em&gt; -citalopram

The serotonin transporter is a sodium and chloride-coupled transporter that &#34;pumps&#34; extracellular serotonin into cells. S-citalopram is a drug ...

科研

生物化学

Isolation and Respiratory Measurements of Mitochondria from Arabidopsis thaliana

Isolation and Respiratory Measurements of Mitochondria from Arabidopsis thaliana

拟南芥线粒体的分离和呼吸测量

Mitochondria are essential organelles involved in numerous metabolic pathways in plants, most notably the production of adenosine triphosphate (ATP) from ...

Caffeine Extraction, Enzymatic Activity and Gene Expression of Caffeine Synthase from Plant Cell Suspensions

植物细胞悬浮液中咖啡因的提取、酶活性及咖啡因合成酶基因的表达

Caffeine (1,3,7-trimethylxanthine) is a purine alkaloid present in popular drinks such as coffee and tea. This secondary metabolite is regarded as a ...

Dissipative Microgravimetry to Study the Binding Dynamics of the Phospholipid Binding Protein Annexin A2 to Solid-supported Lipid Bilayers Using a Quartz Resonator

用石英谐振器研究磷脂结合蛋白附件 a2 与固体支持的脂质层结合动力学的耗散微重法

The dissipative quartz crystal microbalance technique is a simple and label-free approach to measure simultaneously the mass uptake and viscoelastic ...

How to Quantify the Fraction of Photoactivated Fluorescent Proteins in Bulk and in Live Cells

如何定量光活化荧光蛋白在大容量和活细胞中的分数

Photoactivatable and -convertible fluorescent proteins (PA-FPs) have been used in fluorescence live-cell microscopy for analyzing the dynamics of cells ...

Using In Vitro Fluorescence Resonance Energy Transfer to Study the Dynamics Of Protein Complexes at a Millisecond Time Scale

利用体外荧光共振能量转移研究毫秒时间尺度蛋白质配合物的动力学

Proteins are the primary operators of biological systems, and they usually interact with other macro- or small molecules to carry out their biological ...

Expression, Purification, Crystallization, and Enzyme Assays of Fumarylacetoacetate Hydrolase Domain-Containing Proteins

富玛莱酸氢酶含含蛋白质的表达、纯化、结晶和酶测定

Fumarylacetoacetate hydrolase (FAH) domain-containing proteins (FAHD) are identified members of the FAH superfamily in eukaryotes. Enzymes of this ...

Obtaining High-Quality Transcriptome Data from Cereal Seeds by a Modified Method for Gene Expression Profiling

通过基因表达分析的改良方法从谷物种子获取高质量的转录数据

The characterization of gene expression is dependent on RNA quality. In germinating, developing and mature cereal seeds, the extraction of high-quality ...

Transverse Sectioning of Mature Rice (Oryza sativa L.) Kernels for Scanning Electron Microscopy Imaging Using Pipette Tips as Immobilization Support