CN111888797B - 一种利用亲和免疫介质纯化蛋黄抗体的方法 - Google Patents

一种利用亲和免疫介质纯化蛋黄抗体的方法 Download PDF

Info

Publication number
CN111888797B
CN111888797B CN202010663415.2A CN202010663415A CN111888797B CN 111888797 B CN111888797 B CN 111888797B CN 202010663415 A CN202010663415 A CN 202010663415A CN 111888797 B CN111888797 B CN 111888797B
Authority
CN
China
Prior art keywords
asn
lys
gly
ala
leu
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN202010663415.2A
Other languages
English (en)
Other versions
CN111888797A (zh
Inventor
杨严俊
张秀芳
李俊华
常翠华
苏宇杰
顾璐萍
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Youlikang Jiangsu Biological Pharmaceutical Co ltd
Original Assignee
Youlikang Jiangsu Biological Pharmaceutical Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Youlikang Jiangsu Biological Pharmaceutical Co ltd filed Critical Youlikang Jiangsu Biological Pharmaceutical Co ltd
Priority to CN202010663415.2A priority Critical patent/CN111888797B/zh
Publication of CN111888797A publication Critical patent/CN111888797A/zh
Application granted granted Critical
Publication of CN111888797B publication Critical patent/CN111888797B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D15/00Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • B01D15/08Selective adsorption, e.g. chromatography
    • B01D15/26Selective adsorption, e.g. chromatography characterised by the separation mechanism
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/14Extraction; Separation; Purification
    • C07K1/16Extraction; Separation; Purification by chromatography
    • C07K1/22Affinity chromatography or related techniques based upon selective absorption processes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/02Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies from eggs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Peptides Or Proteins (AREA)

Abstract

本发明公开了一种利用亲和免疫介质纯化蛋黄抗体的方法,属于食品技术领域。本发明利用一种硅藻土亲和蛋白标签开发了一种新型的抗体亲和免疫纯化方法。该亲和纯化技术采用廉价的硅藻土助滤剂作为载体,以带有核糖体蛋白L2标签抗原蛋白为偶联配基,利用了核糖体蛋白L2对硅藻土的特异性吸附作用,构建了一种成本低、效率高的亲和免疫纯化方法。高效低成本的特异性蛋黄抗体亲和纯化技术的开发不仅能有效提高特异性蛋黄免疫球蛋白分离提取效率,也能进一步提高蛋黄抗体的附加值和扩大应用领域,这对于提高特异性蛋黄免疫球蛋白在高端生物抗体市场中竞争力具有重要意义。

Description

一种利用亲和免疫介质纯化蛋黄抗体的方法
技术领域
本发明涉及一种利用亲和免疫介质纯化蛋黄抗体的方法,属于食品技术领域。
背景技术
目前,对于抗体的纯化,主要是利用静电性相互作用的离子交换色谱法、利用疏水性相互作用的疏水性色谱法及利用对于抗体的亲和相互作用的蛋白A色谱法等,但是现在通用的抗体的纯化方法均存在操作冗杂、价格昂贵等缺点。
蛋黄免疫球蛋白是一种重要的生物活性抗体,在动物疾病免疫防治、减少或停用动物日粮中亚治疗量的抗生素已经表现出较好的替代效果。部分国内外厂家已经成功的实现了蛋黄免疫球蛋白在生物医药及日用食品领域的应用,开发了能对口腔溃疡有辅助治疗作用的免疫球蛋白口腔喷剂,具有抗龋齿功效的口香糖,具有抗幽门螺杆菌(预防胃炎及胃溃疡)特性的饮料,具有抑菌止痒功效白色念珠菌特异抗体护理液及抗流感病毒牙膏等多款产品。
一直以来,生物蛋白中的色谱或非色谱纯化方法不得不在分离效果、成本和易用性之间进行权衡。由于传统的水相稀释-膜柱分离方法在抗体提取中,尤其是提取的蛋黄抗体中特异性抗体含量低,致使其在工商业、科研、分析检测、理论研究和疾病诊断与防治等方面应用中存在一定的局限性。近年来,亲和免疫层析技术用于分离抗体的技术得到了重视,有报道亲和免疫层析技术由于可从蛋黄样品粗提澄清液中简单过柱处理即可分离出所需的高纯度的特异蛋黄免疫球蛋白。然而亲和免疫层析也存在一些问题,如存在载体发展不足导致价格昂贵(琼脂糖颗粒等)、配基纯度要求过高不易制备和洗脱过程中易造成目的物质失活等缺点。
新种类载体的研究开发及偶联配基的高纯度制备是制约高纯度抗体高效分离技术发展的瓶颈。
发明内容
为了解决上述问题,本发明利用一种硅藻土亲和蛋白标签开发了一种新型的抗体亲和免疫纯化方法。该亲和纯化技术采用廉价的硅藻土助滤剂作为载体,以带有核糖体蛋白L2标签抗原蛋白为偶联配基,利用了核糖体蛋白L2对硅藻土的特异性吸附作用,构建了一种成本低、效率高的亲和免疫纯化方法。高效低成本的特异性蛋黄抗体亲和纯化技术的开发不仅能有效提高特异性蛋黄免疫球蛋白分离提取效率,也能进一步提高蛋黄抗体的附加值和扩大应用领域,这对于提高特异性蛋黄免疫球蛋白在高端生物抗体市场中竞争力具有重要意义。
本发明提供了一种用于抗体纯化的亲和免疫介质,所述亲和免疫介质为吸附融合蛋白的硅藻土,所述融合蛋白为将来源于致病菌或病毒抗原蛋白与核糖体L2蛋白的融合得到的。
在本发明的一种实施方式中,所述核糖体L2蛋白含有如SEQ ID NO.2所示的多肽序列。
在本发明的一种实施方式中,编码所述核糖体L2蛋白含有如SEQ ID NO.7所示的核苷酸序列。
在本发明的一种实施方式中,所述核糖体L2蛋白的氨基酸序列如SEQ ID NO.1所示。
在本发明的一种实施方式中,编码所述核糖体L2蛋白的核苷酸序列如SEQ IDNO.6所示。
在本发明的一种实施方式中,编码所述L2蛋白的基因的获得,可以通过设计PCR引物,从大肠杆菌HB101菌株、BL21(DE3)菌株、TOP10菌等含有L2蛋白菌株进行扩增得到相关基因;也可以按照其氨基酸序列,依据表达细胞的基因密码子偏好,合成相应的基因序列。
本发明提供了一种用于抗体纯化的亲和免疫介质的制备方法,包括如下步骤:(1)合成编码核糖体L2蛋白基因序列;(2)将编码来源于致病菌或病毒的抗原蛋白基因与编码核糖体L2蛋白的基因融合后克隆至带有信号肽的分泌型表达载体中,构建重组表达载体;(3)将所述重组表达载体转化表达宿主,并对表达宿主进行培养表达;(4)将培养结束后所得的发酵液离心,取上清液;(5)将所述上清液与硅藻土混合,使得上清液中的融合蛋白吸附在硅藻土上,得到亲和免疫介质;
或者,包括如下步骤:(1)合成编码核糖体L2蛋白基因序列;(2)将编码来源于致病菌或病毒的抗原蛋白基因与编码核糖体L2蛋白的基因融合后克隆至不含信号肽的胞内表达载体中,构建重组表达载体;(3)将所述重组表达载体转化表达宿主,并对表达宿主进行培养表达;(4)培养结束后破碎宿主细胞,将细胞破碎液离心并取上清液;(5)将所述上清液与硅藻土混合,使得上清液中的融合蛋白吸附在硅藻土上,得到亲和免疫介质。
在本发明的一种实施方式中,所述表达宿主为细菌或真菌。
在本发明的一种实施方式中,所述表达宿主为大肠杆菌。
本发明还提供了一种纯化蛋黄抗体方法,所述方法为:以上述固定有相应抗原蛋白的亲和免疫介质为吸附剂,对蛋黄抗体进行纯化。
本发明还提供了一种蛋黄抗体纯化方法,将含有抗体的清液与固定有相应抗原蛋白的亲和免疫介质混合,静置并抽离清液后,用去离子水和低离子强度盐溶液进行清洗亲和免疫介质,洗去非特异性吸附杂蛋白,再用较高离子强度的盐溶液对亲和免疫介质进行特异性抗体的洗脱,最后经过超滤脱盐得到脱盐后的高纯度特异性抗体。
在本发明的一种实施方式中,所述蛋黄抗体为尿素酶UerB蛋黄抗体、鞭毛鞘膜蛋白HpaA蛋黄抗体、空泡细胞毒素VacA蛋黄抗体和/或细胞毒素CagA蛋黄抗体。
在本发明的一种实施方式中,所述含有抗体的清液的制备方法为:从经过抗原蛋白免疫蛋鸡所产鸡蛋中分离得到蛋黄,将蛋黄与去离子水或缓冲液混合,静置后,抽取上清过滤得到。
在本发明的一种实施方式中,所述含有抗体的清液的制备方法为:从经过抗原蛋白免疫蛋鸡所产鸡蛋中分离得到蛋黄,与4-10倍的经过机械冷却至0-5℃的去离子水或pH值在5.5-7.0缓冲液进行混合,静置3-16小时后抽取上清,经过陶瓷膜微滤后得到清液,与固定有相应抗原亲和免疫介质混合0.5-1小时,抽离清液后,用去离子水和低离子强度盐溶液进行清洗,洗去非特异性吸附杂蛋白,然后再用较高离子强度的盐溶液进行特异性抗体的洗脱,最后经过超滤脱盐得到脱盐后的高纯度特异性蛋黄免疫球蛋白。
在本发明的一种实施方式中,所述抗原蛋白为来自于幽门螺杆菌的尿素酶UerB、鞭毛鞘膜蛋白HpaA、空泡细胞毒素VacA和/或细胞毒素CagA。
在本发明的一种实施方式中,所述尿素酶UerB氨基酸序列如SEQ ID NO.3所示,所述鞭毛鞘膜蛋白HpaA氨基酸序列如SEQ ID NO.4所示,空泡细胞毒素VacA氨基酸序列如SEQID NO.5所示,所述细胞毒素CagA氨基酸序列如SEQ ID NO.11所示。
在本发明的一种实施方式中,编码所述尿素酶UerB基因的核苷酸序列如SEQ IDNO.8所示,编码所述鞭毛鞘膜蛋白HpaA基因的核苷酸序列如SEQ ID NO.9所示,编码所述空泡细胞毒素VacA基因的核苷酸序列如SEQ ID NO.10所示,编码所述细胞毒素CagA基因的核苷酸序列如SEQ ID NO.12所示。
本发明还提供了上述的免疫亲和介质或上述的制备方法或上述的纯化蛋黄抗体的方法在纯化蛋黄抗体中的应用。
本发明的有益效果:
(1)本发明提供了一种全新的纯化蛋黄抗体的方法,采用了廉价硅藻土材料制备亲和免疫介质,因此利用本发明提供的亲和免疫介质进行抗体纯化,解决了亲和免疫基质价格昂贵的问题;采用本发明的方法,既提高了抗体的提取效率和提取纯度,又降低了生产的成本,是一种可行的工业化大规模生产方法。
(2)本发明提供的亲和免疫介质的制备方法利用了核糖体L2蛋白对廉价硅藻土材料的特殊亲和吸附能力,将目的蛋白或多肽与核糖体L2蛋白融合后即可采用常规方法进行重组表达,特异性抗原融合蛋白能通过一步吸附固定化在硅藻土基质上,固定过程不使用任何有毒试剂,固定过程安全、绿色、快速,能有效提高亲和免疫介质的生产效率。
(3)本发明的核糖体蛋白L2能作为重组酶在硅藻土固定化的连接臂,为活性蛋白的固定化提供了更多选择。
附图说明
图1:不同氯化钠浓度下特异性尿素酶蛋黄抗体电泳洗脱图;其中,1-4条带分别为0.25,0.50,0.75和1mol/L氯化钠浓度梯度洗脱下硅藻土亲和介质中流出特异性尿素酶蛋黄抗体成分。
具体实施方式
以下对本发明的优选实施例进行说明,应当理解实施例是为了更好地解释本发明,不用于限制本发明。
下述实施例中涉及的硅藻土购自临江益瑞石硅藻土有限公司。
下述实施例中涉及的培养基如下:
ZYM-5052培养基:每升培养基含蛋白胨10g,酵母提取物5g,磷酸氢二钠4.46,磷酸二氢钾1.7,氯化铵1.33,硫酸钠0.354,甘油2.5,葡萄糖0.25,乳糖1,硫酸镁24.65,痕量元素混合物。
LB培养基:每升培养基含蛋白10g,酵母提取物5g,氯化钠5g NaCl,用1mol/L NaOH调pH至7.4用去离子水定容至1升。
下述实施例中涉及的检测方法如下:
蛋黄免疫球蛋白纯度检测:采用常规聚丙烯酰胺凝胶电泳法,浓缩胶4%,分离胶8%,浓缩电压80V,分离电压120V。用考马斯亮蓝对分离胶进行染色,脱色拍照后采用Quality One软件进行条带光密度分析。
实施例1:融合蛋白表达载体和宿主菌的构建
融合蛋白表达载体的制备:
化学合成编码核糖体L2蛋白的基因(核苷酸序列如SEQ ID NO.6所示)和编码来自于幽门螺杆菌的尿素酶UerB的基因(核苷酸序列如SEQ ID NO.8所示),通过融合PCR将编码L2蛋白的基因和编码来自于幽门螺杆菌尿素酶的基因UerB连接,获得目的基因融合蛋白;将目的基因与pET28a质粒经限制性内切酶BamHI/XhoI酶切后进行连接,得到连接产物;将连接产物转化大肠杆菌E coli BL21(DE3)中,得到转化产物;将转化产物接入ZYM-5052培养基中进行自诱导培养,先37℃培养4小时,再接着在20-28℃下培养12-16小时;培养后提取质粒进行酶切验证以及测序验证,验证正确即获得重组大肠杆菌E coli BL21(DE3)/融合蛋白以及重组质粒pET28a/融合蛋白。
实施例2:硅藻土亲和免疫介质的制备
(1)将实施例1得到的重组大肠杆菌E coli BL21(DE3)/融合蛋白接种于LB培养基上,37℃下过夜培养,得到种子液;将上述种子液以2%的接种量接种于ZYM-5052培养基,37℃、200r/min培养4小时后,在再28度下培养12小时使培养基中菌液浓度度OD达到1.8后收集菌液,离心收集菌体细胞;
(2)将步骤(1)得到的菌体细胞,用pH7.0的10mM/L的磷酸盐缓冲液重悬后,采用超声波或高压均质进行低温细胞破碎,经滤布过滤后,得到澄清的含有融合蛋白的细胞破碎液;
(3)将澄清的细胞破碎液与所选定的硅藻土进行搅拌混合1小时,再通过300目滤布过滤截留硅藻土;
(4)用10倍的去离子水清洗硅藻土基质,再用1.0mol/L的NaCl清洗硅藻土去除非特异性吸附杂蛋白,再用去离子水清洗硅藻土,最后得到固定有抗原蛋白-蛋白L2融合蛋白的硅藻土亲和介质。
实施例3:特异性尿素酶蛋黄抗体的纯化
(1)将经过来自于幽门螺杆菌的尿素酶免疫的蛋鸡所产鸡蛋蛋黄的分离:鸡蛋清洗、干燥后,采用分蛋器分离得到蛋黄;
(2)蛋黄免疫球蛋白粗提:将分离得到的蛋黄与水以料液比1∶4混合,料液pH用柠檬酸调至7.0,温度4℃下静置16小时,抽取静置上清,经陶瓷微滤后得到澄清的粗提液;
(3)特异性蛋黄抗体纯化:将步骤(2)中澄清粗提液与实施例2中得到的固定有特异性抗原蛋白的硅藻土亲和介质混合,搅拌混合1小时后,抽去水相溶液,先用去离子水按1:10料水比清洗硅藻土,再用0.1mol/L的NaCl溶液对硅藻土进行再次清洗,直至无非特异性吸附杂蛋白流出,接着采用1.0mol/L的NaCl溶液洗脱吸附的特异性蛋黄抗体,再经过截留分子量为5万道尔顿的聚砜超滤膜进行超滤脱盐,最后得到脱盐的抗尿素酶特异性蛋黄免疫球蛋白。对得到的特异性蛋黄免疫球蛋白纯度进行测试,结果显示:纯度为93%。
实施例4:特异性鞭毛鞘膜蛋白(HpaA)蛋黄抗体的纯化
具体实施方式同实施例1-3,区别在于,将抗原调整为鞭毛鞘膜蛋白HpaA(编码所述鞭毛鞘膜蛋白HpaA基因的核苷酸序列如SEQ ID NO.9所示),将抗体调整为:抗鞭毛鞘膜蛋白蛋黄抗体,所述抗体的制备方法为:
(1)鸡蛋清洗、干燥后,采用分蛋器分离得到蛋黄;
(2)蛋黄免疫球蛋白粗提:将分离得到的蛋黄与水以料液比1∶6混合,料液pH用柠檬酸调至6.5,温度4℃下静置16小时,抽取静置上清,经陶瓷微滤后得到澄清的粗提液;
(3)特异性蛋黄抗体纯化:将步骤(2)中澄清粗提液与按实施例2方法得到的固定有特异性鞭毛鞘膜蛋白抗原蛋白的硅藻土亲和介质混合,搅拌混合1小时后,抽去水相溶液,先用去离子水按1:20料水比清洗硅藻土,再用0.15mol/L的NaCl溶液对硅藻土进行再次清洗,直至无非特异性吸附杂蛋白流出,接着采用1.0mol/L的NaCl溶液洗脱吸附的特异性蛋黄抗体,再经过截留分子量为5万道尔顿的聚砜超滤膜进行超滤脱盐,对得到的特异性蛋黄免疫球蛋白纯度进行测试,结果显示:纯度为94%。
实施例5:特异性空泡细胞毒素(VacA)蛋黄抗体的纯化
具体实施方式同实施例1-3,区别在于,将抗原调整为空泡细胞毒素VacA(编码空泡细胞毒素VacA基因的核苷酸序列如SEQ ID NO.10所示),将抗体调整为:抗空泡细胞毒素VacA蛋黄抗体,所述抗体的制备方法为:
(1)鸡蛋清洗、干燥后,采用分蛋器分离得到蛋黄;
(2)蛋黄免疫球蛋白粗提:将分离得到的蛋黄与水以料液比1∶10混合,料液pH用柠檬酸调至5.5,温度4℃下静置16小时,抽取静置上清,经陶瓷微滤后得到澄清的粗提液;
(3)特异性蛋黄抗体纯化:将步骤(2)中澄清粗提液与按实施例2方法得到的固定有特异性鞭毛鞘膜蛋白抗原蛋白的硅藻土亲和介质混合,搅拌混合1小时后,抽去水相溶液,先用去离子水按1:20料水比清洗硅藻土,再用0.2mol/L的NaCl溶液对硅藻土进行再次清洗,直至无非特异性吸附杂蛋白流出,接着采用1.0mol/L的NaCl溶液洗脱吸附的特异性蛋黄抗体,再经过截留分子量为5万道尔顿的聚砜超滤膜进行超滤脱盐,对得到的特异性蛋黄免疫球蛋白纯度进行测试,结果显示:纯度为94%。
实施例6:不同浓度的盐溶液对蛋黄抗体纯化的影响
具体实施方式同实施例3,区别在于,分别调整NaCl浓度为0.25,0.50,0.75和1mol/L洗脱液,采用不同浓度NaCl溶液洗脱下蛋黄抗体洗脱特征如图1所示,结果显示,采用1mol/L氯化钠浓度梯度洗脱下,硅藻土亲和介质纯化抗体的效果最佳。
虽然本发明已以较佳实施例公开如上,但其并非用以限定本发明,任何熟悉此技术的人,在不脱离本发明的精神和范围内,都可做各种的改动与修饰,因此本发明的保护范围应该以权利要求书所界定的为准。
SEQUENCE LISTING
<110> 尤丽康(江苏)生物医药有限公司
<120> 一种利用亲和免疫介质纯化蛋黄抗体的方法
<130> BAA200495A
<160> 12
<170> PatentIn version 3.3
<210> 1
<211> 273
<212> PRT
<213> 人工序列
<400> 1
Met Ala Val Val Lys Cys Lys Pro Thr Ser Pro Gly Arg Arg His Val
1 5 10 15
Val Lys Val Val Asn Pro Glu Leu His Lys Gly Lys Pro Phe Ala Pro
20 25 30
Leu Leu Glu Lys Asn Ser Lys Ser Gly Gly Arg Asn Asn Asn Gly Arg
35 40 45
Ile Thr Thr Arg His Ile Gly Gly Gly His Lys Gln Ala Tyr Arg Ile
50 55 60
Val Asp Phe Lys Arg Asn Lys Asp Gly Ile Pro Ala Val Val Glu Arg
65 70 75 80
Leu Glu Tyr Asp Pro Asn Arg Ser Ala Asn Ile Ala Leu Val Leu Tyr
85 90 95
Lys Asp Gly Glu Arg Arg Tyr Ile Leu Ala Pro Lys Gly Leu Lys Ala
100 105 110
Gly Asp Gln Ile Gln Ser Gly Val Asp Ala Ala Ile Lys Pro Gly Asn
115 120 125
Thr Leu Pro Met Arg Asn Ile Pro Val Gly Ser Thr Val His Asn Val
130 135 140
Glu Met Lys Pro Gly Lys Gly Gly Gln Leu Ala Arg Ser Ala Gly Thr
145 150 155 160
Tyr Val Gln Ile Val Ala Arg Asp Gly Ala Tyr Val Thr Leu Arg Leu
165 170 175
Arg Ser Gly Glu Met Arg Lys Val Glu Ala Asp Cys Arg Ala Thr Leu
180 185 190
Gly Glu Val Gly Asn Ala Glu His Met Leu Arg Val Leu Gly Lys Ala
195 200 205
Gly Ala Ala Arg Trp Arg Gly Val Arg Pro Thr Val Arg Gly Thr Ala
210 215 220
Met Asn Pro Val Asp His Pro His Gly Gly Gly Glu Gly Arg Asn Phe
225 230 235 240
Gly Lys His Pro Val Thr Pro Trp Gly Val Gln Thr Lys Gly Lys Lys
245 250 255
Thr Arg Ser Asn Lys Arg Thr Asp Lys Phe Ile Val Arg Arg Arg Ser
260 265 270
Lys
<210> 2
<211> 71
<212> PRT
<213> 人工序列
<400> 2
Met Ala Arg Gly Lys Ala Gly Ala Ala Arg Trp Arg Gly Val Arg Pro
1 5 10 15
Thr Val Arg Gly Thr Ala Met Asn Pro Val Asp His Pro His Gly Gly
20 25 30
Gly Glu Gly Arg Asn Phe Gly Lys His Pro Val Thr Pro Trp Gly Val
35 40 45
Gln Thr Lys Gly Lys Lys Thr Arg Ser Asn Lys Arg Thr Asp Lys Phe
50 55 60
Ile Val Arg Arg Arg Ser Lys
65 70
<210> 3
<211> 569
<212> PRT
<213> 人工序列
<400> 3
Met Lys Lys Ile Ser Arg Lys Glu Tyr Val Ser Met Tyr Gly Pro Thr
1 5 10 15
Thr Gly Asp Lys Val Arg Leu Gly Asp Thr Asp Leu Ile Ala Glu Val
20 25 30
Glu His Asp Tyr Thr Ile Tyr Gly Glu Glu Leu Lys Phe Gly Gly Gly
35 40 45
Lys Thr Leu Arg Glu Gly Met Ser Gln Ser Asn Asn Pro Ser Lys Glu
50 55 60
Glu Leu Asp Leu Ile Ile Thr Asn Ala Leu Ile Val Asp Tyr Thr Gly
65 70 75 80
Ile Tyr Lys Ala Asp Ile Gly Ile Lys Asp Gly Lys Ile Ala Gly Ile
85 90 95
Gly Lys Gly Gly Asn Lys Asp Met Gln Asp Gly Val Lys Asn Asn Leu
100 105 110
Ser Val Gly Pro Ala Thr Glu Ala Leu Ala Gly Glu Gly Leu Ile Val
115 120 125
Thr Ala Gly Gly Ile Asp Thr His Ile His Phe Ile Ser Pro Gln Gln
130 135 140
Ile Pro Thr Ala Phe Ala Ser Gly Val Thr Thr Met Ile Gly Gly Gly
145 150 155 160
Thr Gly Pro Ala Asp Gly Thr Asn Ala Thr Thr Ile Thr Pro Gly Arg
165 170 175
Arg Asn Leu Lys Phe Met Leu Arg Ala Ala Glu Glu Tyr Ser Met Asn
180 185 190
Phe Gly Phe Leu Ala Lys Gly Asn Val Ser Asn Asp Ala Ser Leu Ala
195 200 205
Asp Gln Ile Glu Ala Gly Ala Ile Gly Phe Lys Ile His Glu Asp Trp
210 215 220
Gly Thr Thr Pro Ser Ala Ile Asn His Ala Leu Asp Val Ala Asp Lys
225 230 235 240
Tyr Asp Val Gln Val Ala Ile His Thr Asp Thr Leu Asn Glu Ala Gly
245 250 255
Cys Val Glu Asp Thr Met Ala Ala Ile Ala Gly Arg Thr Met His Thr
260 265 270
Phe His Thr Glu Gly Ala Gly Gly Gly His Ala Pro Asp Ile Ile Lys
275 280 285
Val Ala Gly Glu His Asn Ile Leu Pro Ala Ser Thr Asn Pro Thr Ile
290 295 300
Pro Phe Thr Val Asn Thr Glu Ala Glu His Met Asp Met Leu Met Val
305 310 315 320
Cys His His Leu Asp Lys Ser Ile Lys Glu Asp Val Gln Phe Ala Asp
325 330 335
Ser Arg Ile Arg Pro Gln Thr Ile Ala Ala Glu Asp Thr Leu His Asp
340 345 350
Met Gly Ile Phe Ser Ile Thr Ser Ser Asp Ser Gln Ala Met Gly Arg
355 360 365
Val Gly Glu Val Ile Thr Arg Thr Trp Gln Thr Ala Asp Lys Asn Lys
370 375 380
Lys Glu Phe Gly Arg Leu Lys Glu Glu Lys Gly Asp Asn Asp Asn Phe
385 390 395 400
Arg Ile Lys Arg Tyr Leu Ser Lys Tyr Thr Ile Asn Pro Ala Ile Ala
405 410 415
His Gly Ile Ser Glu Tyr Val Gly Ser Val Glu Val Gly Lys Val Ala
420 425 430
Asp Leu Val Leu Trp Ser Pro Ala Phe Phe Gly Val Lys Pro Asn Met
435 440 445
Ile Ile Lys Gly Gly Phe Ile Ala Leu Ser Gln Met Gly Asp Ala Asn
450 455 460
Ala Ser Ile Pro Thr Pro Gln Pro Val Tyr Tyr Arg Glu Met Phe Ala
465 470 475 480
His His Gly Lys Ala Lys Tyr Asp Ala Asn Ile Thr Phe Val Ser Gln
485 490 495
Ala Ala Tyr Asp Lys Gly Ile Lys Glu Glu Leu Gly Leu Glu Arg Gln
500 505 510
Val Leu Pro Val Lys Asn Cys Arg Asn Ile Thr Lys Lys Asp Met Gln
515 520 525
Phe Asn Asp Thr Thr Ala His Ile Glu Val Asn Pro Glu Thr Tyr His
530 535 540
Val Phe Val Asp Gly Lys Glu Val Thr Ser Lys Pro Ala Asn Lys Val
545 550 555 560
Ser Leu Ala Gln Leu Phe Ser Ile Phe
565
<210> 4
<211> 260
<212> PRT
<213> 人工序列
<400> 4
Met Arg Ala Asn Asn His Phe Lys Asp Phe Ala Trp Lys Lys Cys Leu
1 5 10 15
Leu Gly Ala Ser Val Val Ala Leu Leu Val Gly Cys Ser Pro His Ile
20 25 30
Ile Glu Thr Asn Glu Val Ala Leu Lys Leu Asn Tyr His Pro Ala Ser
35 40 45
Glu Lys Val Gln Ala Leu Asp Glu Lys Ile Leu Leu Leu Arg Pro Ala
50 55 60
Phe Gln Tyr Ser Asp Asn Ile Ala Lys Glu Tyr Glu Asn Lys Phe Lys
65 70 75 80
Asn Gln Thr Thr Leu Lys Val Glu Glu Ile Leu Gln Asn Gln Gly Tyr
85 90 95
Lys Val Ile Ser Val Asp Ser Ser Asp Lys Asp Asp Leu Ser Phe Ser
100 105 110
Gln Lys Lys Glu Gly Tyr Leu Ala Val Ala Met Asn Gly Glu Ile Val
115 120 125
Leu Arg Pro Asp Pro Lys Arg Thr Ile Gln Lys Lys Ser Glu Pro Gly
130 135 140
Leu Leu Phe Ser Thr Gly Leu Asp Lys Met Glu Gly Val Leu Ile Pro
145 150 155 160
Ala Gly Phe Val Lys Val Thr Ile Leu Glu Pro Met Ser Gly Glu Ser
165 170 175
Leu Asp Ser Phe Thr Met Asp Leu Ser Glu Leu Asp Ile Gln Glu Lys
180 185 190
Phe Leu Lys Thr Thr His Ser Ser His Ser Gly Gly Leu Val Ser Thr
195 200 205
Met Val Lys Gly Thr Asp Asn Ser Asn Asp Ala Ile Lys Ser Ala Leu
210 215 220
Asn Lys Ile Phe Ala Asn Ile Met Gln Glu Ile Asp Lys Lys Leu Thr
225 230 235 240
Gln Lys Asn Leu Glu Ser Tyr Gln Lys Asp Ala Lys Glu Leu Lys Asn
245 250 255
Lys Arg Asn Arg
260
<210> 5
<211> 1290
<212> PRT
<213> 人工序列
<400> 5
Met Glu Ile Gln Gln Thr His Arg Lys Ile Asn Arg Pro Leu Val Ser
1 5 10 15
Leu Ala Leu Val Gly Ala Leu Val Ser Ile Thr Pro Gln Gln Ser His
20 25 30
Ala Ala Phe Phe Thr Thr Val Ile Ile Pro Ala Ile Val Gly Gly Ile
35 40 45
Ala Thr Gly Ala Ala Val Gly Thr Val Ser Gly Leu Leu Ser Trp Gly
50 55 60
Leu Lys Gln Ala Glu Glu Ala Asn Lys Thr Pro Asp Lys Pro Asp Lys
65 70 75 80
Val Trp Arg Ile Gln Ala Gly Arg Gly Phe Asn Asn Phe Pro His Lys
85 90 95
Glu Tyr Asp Leu Tyr Lys Ser Leu Leu Ser Ser Lys Ile Asp Gly Gly
100 105 110
Trp Asp Trp Gly Asn Ala Ala Arg His Tyr Trp Val Lys Gly Gly Gln
115 120 125
Trp Asn Lys Leu Glu Val Asp Met Lys Asp Ala Val Gly Thr Tyr Lys
130 135 140
Leu Ser Gly Leu Ile Asn Phe Thr Gly Gly Asp Leu Asp Val Asn Met
145 150 155 160
Gln Lys Ala Thr Leu Arg Leu Gly Gln Phe Asn Gly Asn Ser Phe Thr
165 170 175
Ser Tyr Lys Asp Ser Ala Asp Arg Thr Thr Arg Val Asp Phe Asn Ala
180 185 190
Lys Asn Ile Leu Ile Asp Asn Phe Leu Glu Ile Asn Asn Arg Val Gly
195 200 205
Ser Gly Ala Gly Arg Lys Ala Ser Ser Thr Val Leu Thr Leu Gln Ala
210 215 220
Ser Glu Gly Ile Thr Ser Ser Lys Asn Ala Glu Ile Ser Leu Tyr Asp
225 230 235 240
Gly Ala Thr Leu Asn Leu Ala Ser Ser Ser Val Lys Leu Met Gly Asn
245 250 255
Val Trp Met Gly Arg Leu Gln Tyr Val Gly Ala Tyr Leu Ala Pro Ser
260 265 270
Tyr Ser Thr Ile Asn Thr Ser Lys Val Thr Gly Glu Val Asn Phe Asn
275 280 285
His Leu Thr Val Gly Asp His Asn Ala Ala Gln Ala Gly Ile Ile Ala
290 295 300
Ser Asn Lys Thr His Ile Gly Thr Leu Asp Leu Trp Gln Ser Ala Gly
305 310 315 320
Leu Asn Ile Ile Ala Pro Pro Glu Gly Gly Tyr Lys Asp Lys Pro Lys
325 330 335
Asp Lys Pro Ser Asn Thr Thr Gln Asn Asn Ala Asn Asn Asn Gln Gln
340 345 350
Asn Ser Ala Gln Asn Asn Asn Asn Thr Gln Val Ile Asn Pro Pro Asn
355 360 365
Ser Ala Gln Lys Thr Glu Ile Gln Pro Thr Gln Val Ile Asn Gly Pro
370 375 380
Phe Ala Gly Gly Lys Asp Thr Val Val Asn Ile Asn Arg Ile Asn Thr
385 390 395 400
Asn Ala Asp Gly Thr Ile Arg Val Gly Gly Tyr Lys Ala Ser Leu Thr
405 410 415
Thr Asn Ala Ala His Leu His Ile Gly Lys Gly Gly Ile Asn Leu Ser
420 425 430
Asn Gln Ala Ser Gly Arg Ser Leu Leu Val Glu Asn Leu Thr Gly Asn
435 440 445
Ile Thr Val Asp Gly Pro Leu Arg Val Asn Asn Gln Val Gly Gly Tyr
450 455 460
Ala Leu Ala Gly Ser Asn Ala Asn Phe Glu Phe Lys Ala Gly Thr Asp
465 470 475 480
Thr Lys Asn Gly Thr Ala Thr Phe Asn Asn Asp Ile Ser Leu Gly Arg
485 490 495
Phe Val Asn Leu Lys Val Asp Ala His Thr Ala Asn Phe Lys Gly Ile
500 505 510
Asp Thr Gly Asn Gly Gly Phe Asn Thr Leu Asp Phe Ser Gly Val Thr
515 520 525
Asp Lys Val Asn Ile Asn Lys Leu Ile Thr Ala Ser Thr Asn Val Ala
530 535 540
Ile Lys Asn Phe Asn Ile Asn Glu Leu Leu Val Lys Thr Asn Gly Val
545 550 555 560
Ser Val Gly Glu Tyr Thr His Phe Ser Glu Asp Ile Gly Ser Gln Ser
565 570 575
Arg Ile Asn Thr Val Arg Leu Glu Thr Gly Thr Arg Ser Ile Phe Ser
580 585 590
Gly Gly Val Lys Phe Lys Ser Gly Glu Lys Leu Val Ile Asp Glu Phe
595 600 605
Tyr Tyr Ser Pro Trp Asn Tyr Phe Asp Ala Arg Asn Ile Lys Asn Val
610 615 620
Glu Ile Thr Arg Lys Phe Ala Ser Ser Thr Pro Glu Asn Pro Trp Gly
625 630 635 640
Thr Ser Lys Leu Met Phe Asn Asn Leu Thr Leu Gly Gln Asn Ala Val
645 650 655
Met Asp Tyr Ser Gln Phe Ser Asn Leu Thr Ile Gln Gly Asp Phe Ile
660 665 670
Asn Asn Gln Gly Thr Ile Asn Tyr Leu Val Arg Gly Gly Lys Val Ala
675 680 685
Thr Leu Asn Val Gly Asn Ala Ala Ala Met Met Phe Asn Asn Asp Ile
690 695 700
Asp Ser Ala Thr Gly Phe Tyr Lys Pro Leu Ile Lys Ile Asn Ser Ala
705 710 715 720
Gln Asp Leu Ile Lys Asn Thr Glu His Val Leu Leu Lys Ala Lys Ile
725 730 735
Ile Gly Tyr Gly Asn Val Ser Thr Gly Thr Asn Gly Ile Ser Asn Val
740 745 750
Asn Leu Glu Glu Gln Phe Lys Glu Arg Leu Ala Leu Tyr Asn Asn Asn
755 760 765
Asn Arg Met Asp Thr Cys Val Val Arg Asn Thr Asp Asp Ile Lys Ala
770 775 780
Cys Gly Met Ala Ile Gly Asn Gln Ser Met Val Asn Asn Pro Asp Asn
785 790 795 800
Tyr Lys Tyr Leu Ile Gly Lys Ala Trp Lys Asn Ile Gly Ile Ser Lys
805 810 815
Thr Ala Asn Gly Ser Lys Ile Ser Val Tyr Tyr Leu Gly Asn Ser Thr
820 825 830
Pro Thr Glu Asn Gly Gly Asn Thr Thr Asn Leu Pro Thr Asn Thr Thr
835 840 845
Asn Asn Ala Arg Ser Ala Asn Tyr Ala Leu Val Lys Asn Ala Pro Phe
850 855 860
Ala His Ser Ala Thr Pro Asn Leu Val Ala Ile Asn Gln His Asp Phe
865 870 875 880
Gly Thr Ile Glu Ser Val Phe Glu Leu Ala Asn Arg Ser Lys Asp Ile
885 890 895
Asp Thr Leu Tyr Thr His Ser Gly Ala Lys Gly Arg Asp Leu Leu Gln
900 905 910
Thr Leu Leu Ile Asp Ser His Asp Ala Gly Tyr Ala Arg Gln Met Ile
915 920 925
Asp Asn Thr Ser Thr Gly Glu Ile Thr Lys Gln Leu Asn Ala Ala Thr
930 935 940
Thr Thr Leu Asn Asn Ile Ala Ser Leu Glu His Lys Thr Ser Ser Leu
945 950 955 960
Gln Thr Leu Ser Leu Ser Asn Ala Met Ile Leu Asn Ser Arg Leu Val
965 970 975
Asn Leu Ser Arg Lys His Thr Asn Asn Ile Asp Ser Phe Ala Lys Arg
980 985 990
Leu Gln Ala Leu Lys Asp Gln Arg Phe Ala Ser Leu Glu Ser Ala Ala
995 1000 1005
Glu Val Leu Tyr Gln Phe Ala Pro Lys Tyr Glu Lys Pro Thr Asn
1010 1015 1020
Val Trp Ala Asn Ala Ile Gly Gly Ala Ser Leu Asn Asn Gly Ser
1025 1030 1035
Asn Ala Ser Leu Tyr Gly Thr Ser Ala Gly Val Asp Ala Tyr Leu
1040 1045 1050
Asn Gly Gln Val Glu Ala Ile Val Gly Gly Phe Gly Ser Tyr Gly
1055 1060 1065
Tyr Ser Ser Phe Ser Asn Arg Ala Asn Ser Leu Asn Ser Gly Ala
1070 1075 1080
Asn Asn Thr Asn Phe Gly Val Tyr Ser Arg Ile Phe Ala Asn Gln
1085 1090 1095
His Glu Phe Asp Phe Glu Ala Gln Gly Ala Leu Gly Ser Asp Gln
1100 1105 1110
Ser Ser Leu Asn Phe Lys Ser Ala Leu Leu Gln Asp Leu Asn Gln
1115 1120 1125
Ser Tyr Asn Tyr Leu Ala Tyr Ser Ala Ala Thr Arg Ala Ser Tyr
1130 1135 1140
Gly Tyr Asp Phe Ala Phe Phe Lys Asn Ala Leu Val Leu Lys Pro
1145 1150 1155
Ser Val Gly Val Ser Tyr Asn His Leu Gly Ser Thr Asn Phe Lys
1160 1165 1170
Ser Asn Ser Thr Asn Lys Val Ala Leu Ser Asn Gly Ser Ser Ser
1175 1180 1185
Gln His Leu Phe Asn Ala Ser Ala Asn Val Glu Ala Arg Tyr Tyr
1190 1195 1200
Tyr Gly Asp Thr Ser Tyr Phe Tyr Met Asn Ala Gly Val Leu Gln
1205 1210 1215
Glu Phe Ala Asn Phe Gly Ser Ser Asn Ala Val Ser Leu Asn Thr
1220 1225 1230
Phe Lys Val Asn Ala Ala Arg Asn Pro Leu Asn Thr His Ala Arg
1235 1240 1245
Val Met Met Gly Gly Glu Leu Gln Leu Ala Lys Glu Val Phe Leu
1250 1255 1260
Asn Leu Gly Phe Val Tyr Leu His Asn Leu Ile Ser Asn Ile Gly
1265 1270 1275
His Phe Ala Ser Asn Leu Gly Met Arg Tyr Ser Phe
1280 1285 1290
<210> 6
<211> 819
<212> DNA
<213> 人工序列
<400> 6
atggcagttg ttaaatgtaa accgacatct ccgggtcgtc gccacgtagt taaagtggtt 60
aaccctgagc tgcacaaggg caaacctttt gctccgttgc tggaaaaaaa cagcaaatcc 120
ggtggtcgta acaacaatgg ccgtatcacc actcgtcata tcggtggtgg ccacaagcag 180
gcttaccgta ttgttgactt caaacgcaac aaagacggta tcccggcagt tgttgaacgt 240
cttgagtacg atccgaaccg ttccgcgaac atcgcgctgg ttctgtacaa agacggtgaa 300
cgccgttaca tcctggcccc taaaggcctg aaagctggcg accagattca gtctggcgtt 360
gatgctgcaa tcaaaccagg taacaccctg ccgatgcgca acatcccggt tggttctact 420
gttcataacg tagaaatgaa accaggtaaa ggcggtcagc tggcacgttc cgctggtact 480
tacgttcaga tcgttgctcg tgatggtgct tatgtcaccc tgcgtctgcg ttctggtgaa 540
atgcgtaaag tagaagcaga ctgccgtgca actctgggcg aagttggcaa tgctgagcat 600
atgctgcgcg ttctgggtaa agcaggtgct gcacgctggc gtggtgttcg tccgaccgtt 660
cgcggtaccg cgatgaaccc ggtagaccac ccacatggtg gtggtgaagg tcgtaacttt 720
ggtaagcacc cggtaactcc gtggggcgtt cagaccaaag gtaagaagac ccgcagcaac 780
aagcgtactg ataaattcat cgtacgtcgc cgtagcaaa 819
<210> 7
<211> 213
<212> DNA
<213> 人工序列
<400> 7
atggcacgtg gtaaagcagg tgctgcacgc tggcgtggtg ttcgtccgac cgttcgcggt 60
accgcgatga acccggtaga ccacccacat ggtggtggtg aaggtcgtaa ctttggtaag 120
cacccggtaa ctccgtgggg cgttcagacc aaaggtaaga agacccgcag caacaagcgt 180
actgataaat tcatcgtacg tcgccgtagc aaa 213
<210> 8
<211> 1710
<212> DNA
<213> 人工序列
<400> 8
atgaaaaaga ttagcagaaa agaatatgtt tctatgtatg gccctactac aggcgataaa 60
gtgagattgg gcgatacaga cttgatcgct gaagtagaac atgactacac catttatggc 120
gaagagctta aattcggtgg cggtaaaacc ctaagagaag gcatgagcca atctaacaat 180
cctagcaaag aagaactgga tttaatcatc actaacgctt taatcgtgga ttacaccggt 240
atttataaag cggatattgg tattaaagat ggcaaaatcg ctggcattgg taaaggcggt 300
aacaaagaca tgcaagatgg cgttaaaaac aatcttagcg tgggtcctgc tactgaagcc 360
ttagccggtg aaggtttgat cgtaactgct ggtggtattg acacacacat ccacttcatc 420
tccccccaac aaatccctac agcttttgca agcggtgtaa caaccatgat tggtggcgga 480
actggccctg ctgatggcac taacgcaacc actatcactc caggcagaag aaatttaaaa 540
ttcatgctca gagcggctga agaatattct atgaactttg gtttcttggc taaaggtaac 600
gtttctaacg atgcgagctt agccgatcaa attgaagctg gtgcgattgg ctttaaaatc 660
cacgaagact ggggtaccac tccttctgca atcaatcatg cgttagatgt tgcagacaaa 720
tacgatgtgc aagtcgctat ccacacagac actttgaatg aagccggttg cgtggaagac 780
actatggcag ccattgccgg acgcactatg cacactttcc acactgaagg cgctggcggc 840
ggacacgctc ctgatattat taaagtggcc ggtgaacaca acattctacc tgcttccact 900
aaccccacta tccctttcac cgtgaataca gaagccgaac acatggacat gcttatggtg 960
tgccaccact tggataaaag cattaaagaa gatgttcagt tcgctgattc aaggatccgc 1020
cctcaaacca ttgcggctga agacactttg catgacatgg ggattttctc aatcaccagt 1080
tctgactctc aagctatggg tcgtgtgggt gaagttatca ccagaacttg gcaaacagct 1140
gacaaaaaca aaaaagaatt tggccgcttg aaagaagaaa aaggcgataa cgacaacttc 1200
aggatcaaac gctacttgtc taaatacacc attaacccag cgatcgctca tgggattagc 1260
gagtatgtcg gttctgtaga agtgggcaaa gtggctgact tggtattgtg gagtccagca 1320
ttctttggtg tgaaacccaa catgatcatc aaaggcggat tcattgcatt gagtcaaatg 1380
ggtgatgcga acgcttctat ccctacccca caaccggttt attacagaga aatgttcgct 1440
catcatggta aagctaaata cgatgcaaac atcacttttg tgtctcaagc ggcttatgac 1500
aaaggcatta aagaagaatt agggcttgaa agacaagtgt tgccggtaaa aaattgcaga 1560
aacatcacta aaaaagacat gcaattcaac gacactaccg ctcacattga agtcaatcct 1620
gaaacttacc atgtgttcgt ggatggcaaa gaagtaactt ctaaaccagc caataaagtg 1680
agcttggctc aactctttag cattttctag 1710
<210> 9
<211> 783
<212> DNA
<213> 人工序列
<400> 9
atgagagcaa ataatcattt taaagatttt gcatggaaaa aatgcctttt aggcgcgagc 60
gtggtggctt tgttggtggg atgcagcccg catattattg aaaccaatga agtcgctttg 120
aaattgaatt accatccagc tagcgagaaa gttcaagcgt tagatgaaaa gatcttgctt 180
ttaaggccag cttttcaata cagcgataat attgctaaag agtatgaaaa caaattcaag 240
aatcaaacca cgcttaaggt tgaagagatc ttgcaaaatc aaggctataa ggttattagc 300
gtagatagca gcgataaaga cgatctttct ttttcgcaaa aaaaagaagg gtatttggcc 360
gtcgctatga atggcgaaat tgttttacgc cccgatccta aaaggaccat acagaaaaaa 420
tcagaacccg ggttattatt ctccactggt ttggacaaaa tggaaggggt tttaatcccg 480
gctgggtttg tcaaggttac catactagag cctatgagtg gggaatcttt agattctttt 540
acgatggatt tgagcgagtt ggacattcaa gaaaaattct taaaaaccac ccattcaagc 600
catagcgggg ggttagttag cactatggtt aagggaacgg ataattctaa tgacgcgatc 660
aagagcgctt tgaataagat ttttgcaaat atcatgcaag aaatagacaa aaagctcact 720
caaaagaatt tagaatctta tcaaaaagac gccaaggaat tgaaaaacaa gagaaaccga 780
taa 783
<210> 10
<211> 3873
<212> DNA
<213> 人工序列
<400> 10
atggaaatac aacaaacaca ccgcaaaatc aatcgccctc tggtttctct tgctttagta 60
ggagcgttag tcagcatcac accgcaacaa agtcatgccg cctttttcac aaccgtgatc 120
attccagcca ttgttggggg gatcgctaca ggcgctgctg taggaacggt ctcagggctt 180
cttagctggg ggctcaaaca agccgaagaa gccaataaaa ccccagataa acccgataaa 240
gtttggcgca ttcaagcagg aagaggcttc aataattttc ctcacaagga atacgactta 300
tacaaatccc ttttatccag taagattgat ggaggctggg attgggggaa tgccgctagg 360
cattattggg tcaaaggcgg gcaatggaac aagcttgaag tggatatgaa agacgctgta 420
gggacttata aactttcagg ccttatcaac tttactggtg gggatttaga tgtcaatatg 480
caaaaagcca ctttgcgctt gggccaattc aatggcaatt ctttcacaag ctataaggat 540
agtgctgatc gcaccacgag agtggatttc aacgctaaaa atatcttaat tgataatttt 600
ttagaaatca ataatcgtgt gggttctgga gccgggagga aagccagctc tacggtttta 660
actttgcaag cttcagaagg gatcactagc agtaaaaacg ctgaaatttc tctttatgat 720
ggtgccacgc tcaatttggc ttcaagcagt gttaaattaa tgggtaatgt gtggatgggc 780
cgtttgcaat acgtgggagc gtatctggcc ccttcataca gcacgataaa cacttcaaaa 840
gtgacagggg aagtgaattt taaccatctc actgtgggcg atcacaacgc tgctcaagca 900
ggcattatcg ctagtaacaa gactcatatt ggcacattgg atttgtggca aagcgcgggg 960
ctaaacatta tcgcccctcc agaaggcggt tataaggata aacctaagga taaacctagt 1020
aacaccacgc aaaataatgc taacaacaac caacaaaaca gcgctcaaaa caataataac 1080
actcaggtca ttaacccacc caacagcgcg caaaaaacag aaattcaacc cacgcaagtc 1140
attaatgggc cttttgctgg cggcaaagac acggtggtca atatcaaccg catcaacact 1200
aacgctgatg gcacgattag agtgggaggg tataaagctt ctcttaccac caatgcggct 1260
catttgcata tcggcaaagg cggtatcaat ctgtccaatc aagcgagcgg gcgttcttta 1320
ttggtggaaa atctaaccgg gaatatcacc gttgatgggc ctttaagagt gaataaccaa 1380
gtgggtggtt atgctcttgc aggatcaaac gcgaattttg agtttaaggc tggcacggat 1440
accaaaaacg gcacagccac ttttaataac gatattagtt tgggaagatt tgtgaattta 1500
aaagtggatg ctcatacagc taattttaaa ggtattgata cgggtaatgg tggtttcaac 1560
accttggatt ttagtggcgt tacagacaaa gtcaatatca acaagctcat cacagcttcc 1620
actaatgtgg ccattaaaaa cttcaacatt aatgaattgt tggttaagac caatggggtg 1680
agtgtggggg aatacactca ttttagcgaa gatataggca gtcaatcgcg catcaacacc 1740
gtgcgtttag aaactggcac taggtcaatc ttttctgggg gtgtcaaatt taaaagcggc 1800
gaaaaattgg ttatagatga gttttactat agcccttgga attattttga cgctaggaat 1860
attaaaaatg ttgaaatcac cagaaaattc gcttcttcaa ccccagaaaa cccttggggc 1920
acatcaaaac tcatgtttaa taatctaacc ctgggtcaaa atgcggtcat ggactatagt 1980
caattttcaa atttaaccat tcagggggat tttatcaaca atcaaggcac tatcaactat 2040
ctggtccgag gcgggaaagt ggcaacctta aatgtaggca atgcagcagc tatgatgttt 2100
aataatgata tagacagcgc gaccggattt tacaaaccgc tcatcaagat taacagcgct 2160
caagatctca ttaaaaatac agagcatgtt ttattgaaag cgaaaatcat tggttatggt 2220
aatgtttcta caggtaccaa tggcattagt aatgttaatc tagaagagca attcaaagag 2280
cgcctagccc tttataacaa caataaccgc atggatactt gtgtggtgcg aaatactgat 2340
gacattaaag catgcggtat ggctatcggc aatcaaagca tggtgaacaa ccctgacaat 2400
tacaagtatc ttatcggtaa agcatggaaa aatataggca tcagtaaaac ggctaacggc 2460
tctaaaattt cggtgtatta tttaggcaat tctacgccta ctgagaatgg tggcaatacc 2520
accaacttac ccacaaacac cactaataat gcgcgttctg ctaactacgc tctcgtgaag 2580
aacgctcctt tcgctcacag cgccactcct aatttagtcg ctatcaatca gcatgatttt 2640
ggcactattg agagcgtgtt tgaattggct aaccgctcta aagatattga cacgctttat 2700
actcattcag gtgcaaaagg tagggatctc ttgcaaacct tattgattga tagccatgat 2760
gcgggttacg ctagacaaat gattgataac acaagcaccg gtgaaatcac caagcaattg 2820
aatgcggcca ctaccacttt aaacaacata gccagtttag agcataaaac cagcagctta 2880
caaaccttga gcttgagcaa tgcgatgatt ttaaattctc gtttagtcaa tctctccagg 2940
aagcacacca acaatattga ctcgttcgct aagcgcttac aagctttaaa agatcaaaga 3000
ttcgcttctt tagaaagcgc ggcggaagtg ttgtatcaat ttgcccctaa atatgaaaaa 3060
cctaccaatg tttgggctaa cgctattggg ggagcgagct tgaataatgg ttctaacgct 3120
tcattgtatg gcacaagtgc gggcgtagat gcttacctta acgggcaagt ggaagctatt 3180
gtgggcggtt ttggaagcta tggttatagt tcttttagta atcgtgcgaa ctctcttaac 3240
tctggggcca ataacactaa ttttggcgtg tatagccgta tctttgctaa tcagcacgaa 3300
tttgactttg aagctcaagg ggcgctaggg agtgatcaat caagcttgaa tttcaaaagt 3360
gctttattgc aagatttgaa tcaaagctat aattacttag cctatagcgc tgcaacaaga 3420
gcgagctatg gttatgactt tgcgtttttt aagaacgctt tagtgttaaa accaagcgtg 3480
ggcgtgagct ataaccattt aggttcaacc aactttaaaa gcaacagcac taataaagtg 3540
gctttgagta atggctctag cagtcagcat ctattcaacg ctagcgctaa tgtggaagcg 3600
cgctattatt atggagacac ttcatacttc tatatgaacg ctggagtttt acaagaattt 3660
gctaactttg gttctagcaa tgcggtgtct ttaaacacct ttaaagtgaa tgccgctcgc 3720
aaccctttaa atacccatgc cagagtgatg atgggtgggg aattgcaatt agctaaagaa 3780
gtgtttttga atttgggctt tgtttatttg cacaatttga tttccaatat aggccatttc 3840
gcttccaatt taggaatgag gtatagtttc taa 3873
<210> 11
<211> 1247
<212> PRT
<213> 人工序列
<400> 11
Met Thr Asn Glu Thr Ile Asn Gln Gln Pro Gln Thr Glu Ala Ala Phe
1 5 10 15
Asn Pro Gln Gln Phe Ile Asn Asn Leu Gln Val Ala Phe Leu Lys Val
20 25 30
Asp Asn Ala Val Ala Ser Tyr Asp Pro Asp Gln Lys Pro Ile Val Asp
35 40 45
Lys Asn Asp Arg Asp Asn Arg Gln Ala Phe Asp Gly Ile Ser Gln Leu
50 55 60
Arg Glu Glu Tyr Ser Asn Lys Ala Ile Lys Asn Pro Thr Lys Lys Asn
65 70 75 80
Gln Tyr Phe Ser Asp Phe Ile Asn Lys Ser Asn Asp Leu Ile Asn Lys
85 90 95
Asp Asn Leu Ile Asp Ile Gly Ser Ser Ile Lys Ser Phe Gln Lys Phe
100 105 110
Gly Thr Gln Arg Tyr Arg Ile Phe Thr Ser Trp Val Ser His Gln Asn
115 120 125
Asp Pro Ser Lys Ile Asn Thr Arg Ser Ile Arg Asn Phe Met Glu Asn
130 135 140
Ile Ile Gln Pro Pro Ile Pro Asp Asp Lys Glu Lys Ala Glu Phe Leu
145 150 155 160
Lys Ser Ala Lys Gln Ser Phe Ala Gly Ile Ile Ile Gly Asn Gln Ile
165 170 175
Arg Thr Asp Gln Lys Phe Met Gly Val Phe Asp Glu Phe Leu Lys Glu
180 185 190
Arg Gln Glu Ala Glu Lys Asn Gly Glu Pro Thr Gly Gly Asp Trp Leu
195 200 205
Asp Ile Phe Leu Ser Phe Val Phe Asn Lys Glu Gln Ser Ser Asp Val
210 215 220
Lys Glu Ala Ile Asn Gln Glu Pro Val Pro His Val Gln Pro Asp Ile
225 230 235 240
Ala Thr Thr Thr Thr His Ile Gln Gly Leu Pro Pro Glu Ser Arg Asp
245 250 255
Leu Leu Asp Glu Arg Gly Asn Phe Ser Lys Phe Thr Leu Gly Asp Met
260 265 270
Glu Met Leu Asp Val Glu Gly Val Ala Asp Ile Asp Pro Asn Tyr Lys
275 280 285
Phe Asn Gln Leu Leu Ile His Asn Asn Ala Leu Ser Ser Val Leu Met
290 295 300
Gly Ser His Asn Gly Ile Glu Pro Glu Lys Val Ser Leu Leu Tyr Ala
305 310 315 320
Gly Asn Gly Gly Phe Gly Ala Lys His Asp Trp Asn Ala Thr Val Gly
325 330 335
Tyr Lys Asn Gln Gln Gly Asp Asn Val Ala Thr Leu Ile Asn Val His
340 345 350
Met Lys Asn Gly Ser Gly Leu Val Ile Ala Gly Gly Glu Lys Gly Ile
355 360 365
Asn Asn Pro Ser Phe Tyr Leu Tyr Lys Glu Asp Gln Leu Thr Gly Ser
370 375 380
Gln Arg Ala Leu Ser Gln Glu Glu Ile Arg Asn Lys Ile Asp Phe Met
385 390 395 400
Glu Phe Leu Ala Gln Asn Asn Ala Lys Leu Asp Asn Leu Ser Glu Lys
405 410 415
Glu Lys Glu Lys Phe Gln Asn Glu Ile Glu Asp Phe Gln Lys Asp Ser
420 425 430
Lys Ala Tyr Leu Asp Ala Leu Gly Asn Asp Arg Ile Ala Phe Val Ser
435 440 445
Lys Lys Asp Pro Lys His Ser Ala Leu Ile Thr Glu Phe Gly Lys Gly
450 455 460
Asp Leu Ser Tyr Thr Leu Lys Asp Tyr Gly Lys Lys Ala Asp Arg Ala
465 470 475 480
Leu Asp Arg Glu Lys Asn Val Thr Leu Gln Gly Asn Leu Lys His Asp
485 490 495
Ser Val Met Phe Val Asn Tyr Ser Asn Phe Lys Tyr Thr Asn Ala Ser
500 505 510
Lys Ser Pro Asp Lys Gly Val Gly Val Thr Asn Gly Val Ser His Leu
515 520 525
Asp Ala Gly Phe Ser Lys Val Ala Val Phe Asn Leu Pro Asp Leu Asn
530 535 540
Asn Leu Ala Ile Thr Ser Phe Val Arg Arg Asn Leu Glu Asn Lys Leu
545 550 555 560
Val Thr Glu Gly Leu Ser Leu Gln Glu Ala Asn Lys Leu Ile Lys Asp
565 570 575
Phe Leu Ser Ser Asn Lys Glu Leu Val Gly Lys Ala Leu Asn Phe Asn
580 585 590
Lys Ala Val Ala Asp Ala Lys Asn Thr Gly Asn Tyr Asp Glu Val Lys
595 600 605
Lys Ala Gln Lys Asp Leu Glu Lys Ser Leu Arg Lys Arg Glu His Leu
610 615 620
Glu Lys Glu Val Glu Lys Lys Leu Glu Ser Lys Ser Gly Asn Lys Asn
625 630 635 640
Lys Met Glu Ala Lys Ala Gln Ala Asn Ser Gln Lys Asp Lys Ile Phe
645 650 655
Ala Leu Ile Asn Lys Glu Ala Asn Arg Asp Ala Arg Ala Ile Ala Tyr
660 665 670
Ser Gln Asn Leu Lys Gly Ile Lys Arg Glu Leu Ser Asp Lys Leu Glu
675 680 685
Lys Ile Asn Lys Asp Leu Lys Asp Phe Ser Lys Ser Phe Asp Glu Phe
690 695 700
Lys Asn Gly Lys Asn Lys Asp Phe Ser Lys Ala Glu Glu Thr Leu Lys
705 710 715 720
Ala Leu Lys Gly Ser Val Lys Asp Leu Gly Ile Asn Pro Glu Trp Ile
725 730 735
Ser Lys Val Glu Asn Leu Asn Ala Ala Leu Asn Glu Phe Lys Asn Gly
740 745 750
Lys Asn Lys Asp Phe Ser Lys Val Thr Gln Ala Lys Ser Asp Leu Glu
755 760 765
Asn Ser Val Lys Asp Val Ile Ile Asn Gln Lys Ile Thr Asp Lys Val
770 775 780
Asp Asn Leu Asn Gln Ala Val Ser Met Ala Lys Ala Thr Gly Asp Phe
785 790 795 800
Ser Arg Val Glu Gln Ala Leu Ala Asp Leu Lys Asn Phe Ser Lys Glu
805 810 815
Gln Leu Ala Gln Gln Thr Gln Lys Asn Glu Ser Phe Asn Val Gly Lys
820 825 830
Lys Ser Glu Ile Tyr Gln Ser Val Lys Asn Gly Val Asn Gly Thr Leu
835 840 845
Val Gly Asn Gly Leu Ser Gly Ile Glu Ala Thr Ala Leu Ala Lys Asn
850 855 860
Phe Ser Asp Ile Lys Lys Glu Leu Asn Glu Lys Phe Lys Asn Phe Asn
865 870 875 880
Asn Asn Asn Asn Asn Gly Leu Glu Asn Glu Pro Ile Tyr Ala Lys Val
885 890 895
Asn Lys Lys Lys Thr Gly Gln Val Ala Ser Pro Glu Glu Pro Ile Tyr
900 905 910
Ala Gln Val Ala Lys Lys Val Asn Ala Lys Ile Asp Arg Leu Asn Gln
915 920 925
Ala Ala Ser Gly Leu Gly Gly Val Gly Gln Ala Gly Phe Pro Leu Lys
930 935 940
Arg His Asp Lys Val Asp Asp Leu Ser Lys Val Gly Arg Ser Val Ser
945 950 955 960
Pro Glu Pro Ile Tyr Ala Thr Ile Asp Asp Leu Gly Gly Pro Phe Pro
965 970 975
Leu Lys Arg His Asp Lys Val Asp Asp Leu Ser Lys Val Gly Arg Ser
980 985 990
Val Ser Pro Glu Pro Ile Tyr Ala Thr Ile Asp Asp Leu Gly Gly Pro
995 1000 1005
Phe Pro Leu Lys Arg His Asp Lys Val Asp Asp Leu Ser Lys Val
1010 1015 1020
Gly Arg Ser Val Ser Pro Glu Pro Ile Tyr Ala Thr Ile Asp Asp
1025 1030 1035
Leu Gly Gly Pro Phe Pro Leu Lys Arg His Asp Lys Val Asp Asp
1040 1045 1050
Leu Ser Lys Val Gly Leu Ser Arg Asn Gln Glu Leu Ala Gln Lys
1055 1060 1065
Ile Asp Asn Leu Ser Gln Ala Val Ser Glu Ala Lys Ala Gly Phe
1070 1075 1080
Phe Ser Asn Leu Glu Gln Thr Ile Asp Lys Leu Lys Asp Ser Thr
1085 1090 1095
Lys Tyr Asn Ser Val Asn Leu Trp Val Glu Ser Ala Lys Lys Val
1100 1105 1110
Pro Ala Ser Leu Ser Ala Lys Leu Asp Asn Tyr Ala Thr Asn Ser
1115 1120 1125
His Thr Arg Ile Asn Ser Asn Ile Gln Asn Gly Ala Ile Asn Glu
1130 1135 1140
Lys Ala Thr Gly Met Leu Thr Gln Lys Asn Pro Glu Trp Leu Lys
1145 1150 1155
Leu Val Asn Asp Lys Ile Val Ala His Asn Val Gly Ser Val Pro
1160 1165 1170
Leu Ser Glu Tyr Asp Lys Ile Gly Phe Asn Gln Lys Asn Met Lys
1175 1180 1185
Asp Tyr Ser Asp Ser Phe Lys Phe Ser Thr Lys Leu Asn Asn Ala
1190 1195 1200
Val Lys Asp Val Lys Ser Ser Phe Thr Gln Phe Leu Ala Asn Ala
1205 1210 1215
Phe Ser Thr Gly Tyr Tyr Ser Leu Ala Arg Glu Asn Ala Glu His
1220 1225 1230
Gly Ile Lys Asn Val Asn Thr Lys Gly Gly Phe Gln Lys Ser
1235 1240 1245
<210> 12
<211> 3744
<212> DNA
<213> 人工序列
<400> 12
atgactaacg aaaccattaa ccaacaacca caaaccgaag cggcttttaa cccgcagcaa 60
tttatcaaca atcttcaagt ggcttttctt aaagttgata acgctgtcgc ttcatacgat 120
cctgatcaaa aaccaatcgt tgataagaat gatagggata acaggcaagc ttttgatgga 180
atctcgcaat taagggaaga atactccaat aaagcgatca aaaatcctac caaaaagaat 240
cagtattttt cagactttat caataagagc aatgatttaa tcaacaaaga caatctcatt 300
gatataggtt cttccataaa aagctttcag aaatttggga ctcagcgtta ccgaattttc 360
acaagttggg tgtcccatca aaacgatccg tctaaaatca acacccgatc gatccgaaat 420
tttatggaaa atatcataca accccctatc cctgatgaca aagaaaaagc agagtttttg 480
aaatctgcca aacaatcttt tgcaggaatc attataggga atcaaatccg aacggatcaa 540
aagttcatgg gcgtgtttga tgaattcttg aaagaaaggc aagaagcaga aaaaaatgga 600
gagcctactg gtggggattg gttggatatt tttttatcat ttgtatttaa caaagaacaa 660
tcttctgatg tcaaagaagc aatcaatcaa gaaccagttc cccatgtcca accagatata 720
gccactacca ccacccacat acaaggctta ccgcctgaat ctagggattt gcttgatgaa 780
aggggtaatt tttctaaatt cactcttggc gatatggaaa tgttagatgt tgagggcgtc 840
gccgacattg atcctaatta caagttcaat caattattga ttcacaataa cgctctgtct 900
tctgtgttaa tggggagtca taatggcata gaacctgaaa aagtttcatt attgtatgcg 960
ggcaatggtg gttttggagc caagcacgat tggaacgcca ccgttggtta taaaaaccaa 1020
caaggcgaca atgtggctac actcattaat gtgcatatga aaaacggcag tggcttagtc 1080
atagcaggtg gtgagaaagg gattaacaac cctagttttt atctctacaa agaagaccaa 1140
ctcacaggct cacaacgagc attgagtcaa gaagagatcc gaaacaaaat agatttcatg 1200
gaatttcttg cacaaaacaa tgctaaatta gacaacttga gcgagaaaga gaaagaaaaa 1260
ttccaaaatg agattgaaga ttttcaaaaa gactctaagg cttatttaga cgccctaggg 1320
aatgatcgta ttgcctttgt ttctaaaaaa gacccaaaac attcagcttt aattactgag 1380
tttggtaagg gggatttgag ctacactctc aaagattatg ggaaaaaagc agatagagct 1440
ttagataggg agaaaaatgt tactcttcaa ggtaacctaa aacatgatag cgtgatgttt 1500
gttaattatt ctaatttcaa atacaccaac gcctccaaga gtcctgataa gggtgtaggc 1560
gttacaaatg gcgtttccca tttagacgca ggctttagca aggtagctgt ctttaatttg 1620
cctgatttaa ataatctcgc tatcactagt ttcgtaaggc ggaatttaga gaataaacta 1680
gtcactgaag gattgtccct acaagaagct aataagctta tcaaagattt tttgagcagc 1740
aacaaagaat tggttggaaa agctttaaac ttcaataaag ctgtagctga cgctaaaaac 1800
acaggcaact atgatgaagt gaaaaaagct cagaaagatc ttgaaaaatc tctaaggaaa 1860
cgagagcatt tagagaaaga agtagagaaa aaattggaga gcaaaagcgg caacaaaaat 1920
aaaatggaag cgaaagctca agctaacagc caaaaagata agatttttgc gttgatcaat 1980
aaagaggcta atagggacgc aagagcaatc gcttactctc agaatcttaa aggcatcaaa 2040
agggaattgt ctgataaact tgaaaaaatc aacaaggatt tgaaagactt tagtaaatct 2100
tttgatgaat tcaaaaatgg caaaaataag gattttagca aggcagaaga aacgctaaaa 2160
gcccttaaag gctcggtgaa agatttaggt atcaatccgg aatggatttc aaaagttgaa 2220
aaccttaatg cagctttgaa tgaattcaaa aatggcaaaa ataaggattt cagcaaggta 2280
acgcaagcaa aaagcgacct tgaaaattcc gttaaagatg tgatcatcaa tcaaaagata 2340
acggataaag ttgacaatct caatcaagcg gtatcaatgg ctaaagcaac gggtgatttc 2400
agtagggtag agcaagcgtt agccgatctc aaaaacttct caaaggagca attggctcaa 2460
caaactcaaa aaaatgaaag tttcaatgtt ggaaaaaaat ctgaaatata tcaatccgtt 2520
aagaatggtg tgaacggaac cctagtcggt aatgggttat ctggaataga ggccacagct 2580
ctcgccaaaa atttttcgga tatcaagaaa gaattgaatg agaaatttaa aaatttcaat 2640
aacaataaca ataatggact cgaaaacgaa cccatttatg ctaaagttaa taaaaagaaa 2700
acaggacaag tagctagccc tgaagaaccc atttacgctc aagttgctaa aaaggtgaat 2760
gcaaaaattg accgactcaa tcaagcagca agtggtttgg gtggtgtagg gcaagcgggc 2820
ttccctttga aaaggcatga taaagttgat gatctcagta aggtagggcg atcagttagc 2880
cctgaaccca tttatgctac gattgatgat ctcggcggac ctttcccttt gaaaaggcat 2940
gataaagttg atgatctcag taaggtaggg cgatcagtta gccctgaacc catttatgct 3000
acgattgatg atctcggcgg acctttccct ttgaaaaggc atgataaagt tgatgatctc 3060
agtaaggtag ggcgatcagt tagccctgaa cccatttatg ctacgattga tgatctcggc 3120
ggacctttcc ctttgaaaag gcatgataaa gttgatgatc tcagtaaggt agggctttca 3180
aggaatcaag aattggctca gaaaattgac aatctcagtc aagcggtatc agaagctaaa 3240
gcaggttttt ttagcaatct agagcaaacg atagacaagc tcaaagattc tacaaaatac 3300
aattctgtga atctatgggt tgaaagtgca aaaaaagtgc ctgctagttt gtcagcgaaa 3360
ctagacaatt acgctactaa cagccacaca cgcattaata gcaatatcca aaatggagca 3420
atcaatgaaa aagcgaccgg tatgctaacg caaaaaaacc ctgagtggct caagctcgtg 3480
aatgataaga tagttgcgca taatgtggga agcgttcctt tgtcagagta tgataaaatt 3540
ggcttcaacc agaagaatat gaaagattat tctgattcgt tcaagttttc caccaagttg 3600
aacaatgctg taaaagacgt taagtctagc tttacgcaat ttttagccaa tgcattttct 3660
acaggatatt actccttggc gagggaaaat gcggagcatg gaatcaaaaa tgttaataca 3720
aaaggtggtt tccaaaaatc ttaa 3744

Claims (9)

1.一种用于纯化特异性蛋黄抗体的亲和免疫介质,其特征在于,所述亲和免疫介质为吸附融合蛋白的硅藻土,所述融合蛋白为将来源于致病菌或病毒的抗原蛋白与核糖体L2蛋白融合得到的;所述核糖体L2蛋白含有如SEQ ID NO.2所示的多肽序列。
2.如权利要求1所述的亲和免疫介质,其特征在于,所述核糖体L2蛋白的氨基酸序列如SEQ ID NO.1所示。
3.一种权利要求1所述的亲和免疫介质的制备方法,其特征在于,包括如下步骤:(1)合成编码核糖体L2蛋白基因序列;(2)将编码来源于致病菌或病毒的抗原蛋白基因与编码核糖体L2蛋白的基因融合后克隆至带有信号肽的分泌型表达载体中,构建重组表达载体;(3)将所述重组表达载体转化表达宿主,并对表达宿主进行培养表达;(4)将培养结束后所得的发酵液离心,取上清液;(5)将所述上清液与硅藻土混合,使得上清液中的融合蛋白吸附在硅藻土上,得到亲和免疫介质;
或者,包括如下步骤:(1)合成编码核糖体L2蛋白基因序列;(2)将编码来源于致病菌或病毒的抗原蛋白基因与编码核糖体L2蛋白的基因融合后克隆至不含信号肽的胞内表达载体中,构建重组表达载体;(3)将所述重组表达载体转化表达宿主,并对表达宿主进行培养表达;(4)培养结束后破碎宿主细胞,将细胞破碎液离心并取上清液;(5)将所述上清液与硅藻土混合,使得上清液中的融合蛋白吸附在硅藻土上,得到亲和免疫介质。
4.一种纯化特异性蛋黄抗体方法,其特征在于,所述方法为:以固定有相应抗原蛋白的权利要求1或2所述的亲和免疫介质为吸附剂,对蛋黄抗体进行纯化。
5.如权利要求4所述的纯化特异性蛋黄抗体方法,其特征在于,将含有抗体的清液与固定有相应抗原蛋白的亲和免疫介质混合,静置并抽离清液后,用去离子水和低离子强度盐溶液进行清洗亲和免疫介质,洗去非特异性吸附杂蛋白,再用1.0 mol/L的盐溶液对亲和免疫介质进行特异性抗体的洗脱,最后经过超滤脱盐得到脱盐后的高纯度特异性抗体。
6.如权利要求4所述的纯化特异性蛋黄抗体方法,其特征在于,所述蛋黄抗体包括尿素酶UerB蛋黄抗体、鞭毛鞘膜蛋白HpaA蛋黄抗体、空泡细胞毒素VacA蛋黄抗体和/或细胞毒素CagA蛋黄抗体。
7.如权利要求5所述的纯化特异性蛋黄抗体方法,其特征在于,所述含有抗体的清液的制备方法为:从经过抗原蛋白免疫蛋鸡所产鸡蛋中分离得到蛋黄,将蛋黄与去离子水或缓冲液混合,静置后,抽取上清液 过滤得到。
8.如权利要求4所述的纯化特异性蛋黄抗体方法,其特征在于,所述抗原蛋白包括来自于幽门螺杆菌的尿素酶UerB、鞭毛鞘膜蛋白HpaA、空泡细胞毒素VacA和/或细胞毒素CagA。
9.权利要求1或2任一所述的亲和免疫 介质或权利要求3所述的制备方法或权利要求4或5所述的纯化特异性 蛋黄抗体的方法在纯化蛋黄抗体中的应用。
CN202010663415.2A 2020-07-10 2020-07-10 一种利用亲和免疫介质纯化蛋黄抗体的方法 Active CN111888797B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010663415.2A CN111888797B (zh) 2020-07-10 2020-07-10 一种利用亲和免疫介质纯化蛋黄抗体的方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010663415.2A CN111888797B (zh) 2020-07-10 2020-07-10 一种利用亲和免疫介质纯化蛋黄抗体的方法

Publications (2)

Publication Number Publication Date
CN111888797A CN111888797A (zh) 2020-11-06
CN111888797B true CN111888797B (zh) 2022-05-10

Family

ID=73192236

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010663415.2A Active CN111888797B (zh) 2020-07-10 2020-07-10 一种利用亲和免疫介质纯化蛋黄抗体的方法

Country Status (1)

Country Link
CN (1) CN111888797B (zh)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116068170B (zh) * 2022-09-28 2023-09-15 北京金沃夫生物工程科技有限公司 一种检测幽门螺旋杆菌的试纸和试剂盒

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0341733A2 (en) * 1988-05-13 1989-11-15 Dong-A Pharm. Co., Ltd. Isolation of HBsAg by immunoaffinity chromatography using the anti-idiotype antibody as an eluting agent
CN101817880A (zh) * 2009-12-26 2010-09-01 中国海洋大学 一种特异性卵黄抗体的免疫亲和层析纯化方法
CN102676562A (zh) * 2012-04-21 2012-09-19 大连理工大学 一种对抗体具有广谱吸附能力的融合蛋白制备方法及应用
CN103060359A (zh) * 2012-12-20 2013-04-24 江南大学 一种利用缩短后l2蛋白标签纯化重组蛋白的方法
CN106140099A (zh) * 2015-04-17 2016-11-23 北京美正生物科技有限公司 一种分离纯化乳铁蛋白的免疫亲和柱及其制备方法和用途
CN106188279A (zh) * 2016-07-07 2016-12-07 南昌大学 一种免疫库来源的特异性识别免疫球蛋白Fc段的纳米抗体

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0341733A2 (en) * 1988-05-13 1989-11-15 Dong-A Pharm. Co., Ltd. Isolation of HBsAg by immunoaffinity chromatography using the anti-idiotype antibody as an eluting agent
CN101817880A (zh) * 2009-12-26 2010-09-01 中国海洋大学 一种特异性卵黄抗体的免疫亲和层析纯化方法
CN102676562A (zh) * 2012-04-21 2012-09-19 大连理工大学 一种对抗体具有广谱吸附能力的融合蛋白制备方法及应用
CN103060359A (zh) * 2012-12-20 2013-04-24 江南大学 一种利用缩短后l2蛋白标签纯化重组蛋白的方法
CN106140099A (zh) * 2015-04-17 2016-11-23 北京美正生物科技有限公司 一种分离纯化乳铁蛋白的免疫亲和柱及其制备方法和用途
CN106188279A (zh) * 2016-07-07 2016-12-07 南昌大学 一种免疫库来源的特异性识别免疫球蛋白Fc段的纳米抗体

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Accession NO:WP_000301864.1;Gene Bank;《Gene Bank Database》;20190620;第1页 *
Accession NO:WP_049291856.1;Gene Bank;《Gene Bank Database》;20190616;第1页 *

Also Published As

Publication number Publication date
CN111888797A (zh) 2020-11-06

Similar Documents

Publication Publication Date Title
CN104059133A (zh) 一类突变的具有高耐碱特性的蛋白a及其应用
CN107245494A (zh) Aβ42在大肠杆菌中的高效可溶性表达及纯化方法
CN105296506B (zh) 以硫磺菌蘑菇凝集素n-乙酰氨基乳糖胺结合域作为融合标签的目标蛋白表达与纯化方法
AU7643387A (en) A neisseria gonorrhoeae lectin useful as a vaccine and diagnostic marker and means for producing this lectin
CN110845582B (zh) 一种猫细小病毒重组蛋白及其单克隆抗体的制备
CN115785237B (zh) 一种重组肉毒杆菌毒素及其制备方法
CN111647607A (zh) 一种利用大肠杆菌高效表达并分泌人生长激素的方法
CN111888797B (zh) 一种利用亲和免疫介质纯化蛋黄抗体的方法
CN108314710B (zh) 肺炎支原体重组抗原及其应用
CN104610443B (zh) 一种高稳定性重组降钙素原、制备方法及用途
CN108059676B (zh) 一种抗人神经生长因子scFv抗体及制备方法
EP0372352B1 (en) Aequorin fused with a protein having a specific-binding activity, its preparation, its purification and detection method by its use
CN110938151B (zh) 用于表达甲状旁腺素pth的融合蛋白及重组质粒、重组工程菌
CN110028581B (zh) 一种微囊藻毒素抗体Fab片段的制备方法和应用
CN104356238B (zh) 一种重组蛋白a亲和配基的定点固定化方法
CN109384834A (zh) 重组Protein A蛋白及其高效表达和应用
CN105949320A (zh) 埃可病毒1型vp1蛋白特异性抗原表位及其融合蛋白的制备、应用
RU2141531C1 (ru) Способ получения рекомбинантного инсулина человека
CN110903359B (zh) 一种空肠弯曲菌重组蛋白及其单克隆抗体的制备
CN105906716B (zh) 埃可病毒9型vp1蛋白特异性抗原表位及其融合蛋白的制备、应用
CN109762065B (zh) 针对河流弧菌的单域重链抗体Nb72
CN112094853A (zh) 白斑综合征病毒vp28基因、重组蛋白、多克隆抗体及制备方法和应用
CN108218996A (zh) 重组蛋白及其纯化制备方法
CN107033224B (zh) 一种口蹄疫病毒灭活抗原纯化浓缩方法
CN114716567A (zh) 一种嵌合体抗原和抗金环蛇蛇毒制剂的制备方法及其应用

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant