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一种高效表达具有高活性及稳定性的重组TEV酶及其制备、测定方法和应用

文献发布时间:2023-06-19 13:45:04


一种高效表达具有高活性及稳定性的重组TEV酶及其制备、测定方法和应用

技术领域

本发明涉及重组蛋白技术领域,具体涉及一种高效表达具有高活性及稳定性的重组TEV酶及其制备、测定方法和应用。

背景技术

重组蛋白的表达被广泛应用于生物工程当中,包括蛋白纯化,定位及功能分析的等。根据表达系统的不同,主要分为大肠杆菌表达系统、酵母表达系统、昆虫细胞表达系统以及哺乳动物细胞表达系统。其中酵母表达系统、昆虫表达系统以及哺乳动物表达系统属于真核表达系统,大肠杆菌表达系统属于原核表达系统。原核表达系统相较于真核表达系统拥有诸多优势,包括遗传背景清晰、繁殖快、成本低、抗污染能力强、表达量高、商品化载体和菌株种类齐全、适用范围广等。但大肠杆菌表达系统由于缺少真核生物中翻译后修饰所需的酶类,并且蛋白表达量过高或合成速度过快,以至于没有足够的时间进行折叠,二硫键不能正确配对,导致蛋白常常以包涵体的形式存在。包涵体的表达虽然有利于目的蛋白的初步纯化,但无生物活性的不溶性蛋白要经过变性及复性,使其重新折叠成具有天然蛋白构象和良好的生物活性的蛋白质是非常困难的。

为了解决该问题,利用DNA体外重组技术,在目的蛋白N端或C端添加可融合表达的特定蛋白、多肽或寡肽标签。通过添加融合标签,既能保留天然蛋白的大部分结构,又能实现提高蛋白溶解度、稳定性、促进其分泌等目的,并且重组蛋白通过融合标签与包被在固相基质上的特异配基结合,可使重组蛋白定向固定得以纯化,大大简化了重组蛋白的纯化过程。然而,研究发现大多数融合标签对蛋白的生物功能及结构都存在潜在干扰,因此常常需要在融合标签及目的蛋白之间添加一段特异的蛋白酶识别序列,并在后续纯化过程中使用相应的蛋白酶将其切割分开,最终获得目的蛋白。目前常用的切割融合标签及目的蛋白的工具酶有凝血酶,肠激酶,因子Xa,然而这些哺乳动物类的蛋白酶没有严格的序列特异性,可能会切割目的蛋白的氨基酸序列。从而对一些病毒类来源的蛋白酶研究表明其具有更好的序列特异性。

TEV蛋白酶是来源于烟草蚀纹病毒(TEV)的Nla蛋白酶,具有很强的位点特异性,能够识别EXXYXQ(G/S)的七氨基酸序列,TEV酶具有广泛的pH和温度耐受性,pH耐受范围在4-8.0;耐受温度在4-34℃,因此可作为理想的工具酶使用(Sun C,Liang J,Shi R,etal.Tobacco etch virus protease retains its activity in various buffers and inthe presence of diverse additives.[J].Protein Expr Purif,2012,82(1):226-231.)。然而,野生型的TEV蛋白酶在大肠杆菌中表达及纯化中存在三个问题:自我剪切、稀有密码子以及可溶性差。野生型TEV酶在纯化及储存过程中,会在特定位点自我剪切,不仅大幅度降低了TEV酶的活性,并且由于TEV蛋白酶截短体的存在,使得后续纯化过程中很难将TEV蛋白酶截短体与目的蛋白分开,蛋白酶纯度得不到保障(Kapust R B,Tzsér

发明内容

本发明的目的在于克服现有技术的不足,提供了一种高效表达具有高活性及稳定性的重组TEV酶及其制备、测定方法和应用。

本发明通过以下技术方案来实现上述目的:

本发明提供了一种高效表达具有高活性及稳定性的重组TEV酶,包括编码TEV蛋白酶的氨基酸序列或其突变序列,所述编码TEV蛋白酶的氨基酸序列或其突变序列的N端融合有CL7标签,所述编码TEV蛋白酶的氨基酸序列或其突变序列的C端融合有多聚精氨酸标签。

进一步改进在于,所述CL7标签为依次顺式连接的His6-CL7-GGS多肽序列,所述CL7的氨基酸序列如SEQ ID NO.1所示。

进一步改进在于,所述多聚精氨酸标签为RRRGRRRGRRRG多肽序列组成。

进一步改进在于,所述编码TEV蛋白酶的氨基酸序列的突变序列为TEV蛋白酶的氨基酸序列中包括如下a)-f)中至少一种或多种突变:

a)TEV蛋白酶的第219位氨基酸残基由缬氨酸突变为天冬酰胺;

b)TEV蛋白酶的第17位氨基酸残基由苏氨酸突变为丝氨酸;

c)TEV蛋白酶的第56位氨基酸残基由亮氨酸突变为缬氨酸;

d)TEV蛋白酶的第68位氨基酸残基由天冬酰胺突变为天冬氨酸;

e)TEV蛋白酶的第77位氨基酸残基由异亮氨酸突变为缬氨酸;

f)TEV蛋白酶的第135位氨基酸残基由丝氨酸突变为甘氨酸。

进一步改进在于,所述编码TEV蛋白酶的氨基酸序列的突变序列为TEV蛋白酶的氨基酸序列中包括a)-f)六种突变。

进一步改进在于,所述编码TEV蛋白酶的氨基酸序列如SEQ ID NO.2所示。

本发明还提供了一种多核苷酸序列,所述多核苷酸序列为用于编码上述高效表达具有高活性及稳定性的重组TEV酶的氨基酸序列的核苷酸序列。

进一步改进在于,所述多核苷酸序列如SEQ ID NO.3所示。

本发明还提供了一种重组质粒,所述重组质粒为将上述多核苷酸序列插入到表达载体中,且能够翻译表达出上述的重组TEV酶的重组质粒。

进一步改进在于,所述表达载体为pET-28a载体。

本发明还提供了一种重组工程菌,所述重组工程菌包含上述重组质粒或基因组中整合有上述多核苷酸序列。

进一步改进在于,所述重组工程菌为大肠杆菌BL21(DE3)或T7 Express细胞。

本发明还提供了一种上述重组TEV酶的制备方法,步骤包括:

(1)以烟草蚀纹病毒TEV的基因序列为模板,通过PCR扩增技术获得TEV蛋白酶突变体的基因,将其基因构建在pET-28a载体上,获得重组质粒。

(2)利用大肠杆菌原核表达系统表达重组质粒,并利用Ni-NTA柱和亲和层析纯化获得重组TEV酶蛋白。

进一步改进在于,纯化重组TEV酶蛋白的缓冲液为50mMTris-HCl,500mMNaCl,10%glycerol,20mM imidazole。

本发明还提供了一种上述重组TEV酶活性测定方法,使用荧光共振能量转移方法检测所述TEV蛋白酶活性。

本发明还提供了一种上述重组TEV酶热稳定性测定方法,通过测定突变体蛋白溶解温度Tm值的变化判断蛋白稳定性,Tm值增大,蛋白越稳定。

本发明的有益效果在于:与现有重组TEV蛋白酶相比,本发明所提供的重组TEV蛋白酶不仅能够克服野生型TEV蛋白酶在表达过程中对自身特异位点进行剪切而导致的蛋白稳定性及活性降低的缺陷,还具备更高的蛋白产量,更好的蛋白稳定性以及更高的活性,更加适合大规模生产及工业使用。

本发明提供的重组TEV蛋白酶在TEV蛋白酶的N端和C端均融合了氨基酸多肽序列,其中的N端多肽序列为His-CL7-GGS,C端的多肽序列为RRRGRRRGRRRG。本发明提供的重组TEV蛋白酶对野生型TEV蛋白酶进行了突变,突变至少6个氨基酸残基。

本发明提供的重组TEV蛋白酶通过在N端添加CL7标签增加了TEV蛋白酶的表达量;通过在C端添加RRRGRRRGRRRG标签增加了TEV蛋白酶的溶解性;通过在N端和C端分别添加CL7和RRRGRRRGRRRG标签,优化突变氨基酸的数量增加了TEV蛋白酶的活性;通过在N端和C端分别添加CL7和RRRGRRRGRRRG标签,优化突变氨基酸的数量提高了TEV蛋白酶的Tm值、增加了蛋白的稳定性。

与现有TEV突变体(cTEV)相比,本发明提供的TEV蛋白酶突变体具有如下有益效果:

1、超高的蛋白产量。本发明提供的TEV蛋白酶突变体蛋白产量可高达61.95mg/L,并且蛋白纯度也可达到90%,而同等条件下,现有TEV蛋白酶突变体(cTEV)的产量仅为32.5mg/L。

2、较好的活性。本发明提供的TEV蛋白酶突变体活性测定为8.09×10^

3、更高的热稳定性。本发明提供的TEV蛋白酶突变体Tm值为55.8℃。而同等条件下,现有TEV蛋白酶突变体(cTEV)Tm值为42.05℃,本发明所述提供的TEV蛋白酶突变体活性相比于TEV蛋白酶突变体(cTEV)具有更好的蛋白热稳定性,能够在更宽的温度范围内保持良好蛋白酶活性。

附图说明

图1为cTEV、prTEV蛋白酶在T7 Express细胞中表达纯化结果;

图2为cTEV、prTEV蛋白酶在BL21细胞中表达纯化结果;

图3为prTEV蛋白酶的质谱和分子筛检测检测结果;

图4为不同TEV蛋白酶突变体活性检测结果;

图5为cTEV、prTEV蛋白酶热稳定性测定结果;

图6为4℃下cTEV、prTEV蛋白酶酶切效果验证结果;

图7为室温下cTEV、prTEV蛋白酶酶切效果验证结果。

具体实施方式

下面结合附图对本申请作进一步详细描述,有必要在此指出的是,以下具体实施方式只用于对本申请进行进一步的说明,不能理解为对本申请保护范围的限制,该领域的技术人员可以根据上述申请内容对本申请作出一些非本质的改进和调整。

1、材料

本实施例所用方法如无特别说明均为本领域的技术人员所知晓的常规方法,所用的试剂等材料,如无特别说明,均为市售购买产品。

2、方法

2.1质粒构建及小试表达

本发明使用的所有质粒均使用常规的分子生物学手段进行引物设计,PCR及载体片段重组构建得到,所有重组质粒均经测序验证与目标序列完全一致。

本发明通过使用多种常规表达载体,不断优化N端及C端融合多肽序列,并设计了不同氨基酸序列突变体及其组合构建了多个重组质粒,最终得到了同时具备高产量,高稳定性及高活性三种特征的重组TEV蛋白酶。

本发明所述重组TEV蛋白酶的基因序列是通过常规PCR获得,烟草蚀纹病毒TEV的基因序列如SEQ ID NO.3所示,分别在N端和C端融合了多肽序列或标签,其中的N端多肽序列为His-CL7-GGS,CL7的氨基酸序列如SEQ ID NO.1所示,C端的多肽序列为RRRGRRRGRRRG,同时突变了如下6个氨基酸残基:第17位氨基酸残基由苏氨酸突变为丝氨酸;第56位氨基酸残基由亮氨酸突变为缬氨酸;第68位氨基酸残基由天冬酰胺突变为天冬氨酸;第77位氨基酸残基由异亮氨酸突变为缬氨酸;第219位氨基酸残基由缬氨酸突变为天冬酰胺;第135位氨基酸残基由丝氨酸突变为甘氨酸,重组TEV蛋白酶编号prTEV。

同时根据现有酶活性较高的突变体进行改造(Kapust R B,Tzsér József,Fox JD,et al.Tobacco etch virus protease:mechanism of autolysis and rationaldesign of stable mutants with wild-type catalytic proficiency[J].ProteinEngineering,2001(12):993.),获得编号为cTEV的重组TEV蛋白酶,所述cTEV与本发明prTEV蛋白酶突变体不同的是cTEV仅突变一个位点,即将第219位氨基酸残基由丝氨酸突变为缬氨酸,N端标签为MBP-TEV-His,C端助溶标签为5R。

2.1.1 prTEV、cTEV重组TEV蛋白酶质粒转化大肠杆菌感受态细胞

从-80℃冰箱取出感受态细胞于冰上化冻,超净台内将所述重组质粒使用常规分子生物学手段分别转化BL21(DE3)和T7 Express大肠杆菌感受态细胞,42℃热击90s后将感受态细胞静置5分钟后,将感受态涂布在LB固体平板上,37℃倒置过夜培养。

2.1.2 prTEV、cTEV重组TEV蛋白酶小量表达

挑取过夜培养的单克隆菌落至5mlLB液体培养基中,37℃培养,待菌液OD

2.2蛋白的大量表达及纯化

2.2.1 prTEV重组TEV蛋白酶大量表达

将小试明显表达的菌株接中至50ml LB液体培养基中37℃培养过夜,将过夜培养的细菌按1:100的比例接至1L LB液体培养基中,37℃培养至菌液OD600为0.6-0.8时加入0.5mMIPTG16℃培养过夜,5000rpm离心收集菌体。

2.2.2 prTEV重组TEV蛋白酶纯化

将收集的菌块进行称重,按照1:10比例加入相应体积的裂解缓冲液(50mM Tris-HCl(pH8.0),500mM NaCl,10%glycerol,20mM imidazole),使用高压均质机破碎菌体,16000rpm高速离心收集上清。使用亲和层析HisFF富集纯化蛋白,纯化前先用裂解buffer平衡HisFF柱,将所有细胞上清与HisFF结合后,用不同梯度的咪唑溶液进行洗脱,收集不同梯度咪唑洗脱下的蛋白进行SDS-PAGE检测,收集纯度较好的蛋白用Nanodrop测定蛋白浓度,计算蛋白产量。蛋白纯化结果如图1和图2。根据纯化的结果可知prTEV突变体TEV蛋白酶在T7 Express和BL21细胞中比现有的cTEV蛋白酶的表达量要高。

2.2.3 prTEV重组TEV蛋白酶质量检测

将咪唑洗脱下的蛋白取少量分别进行质谱和分子筛检测。质谱检测结果显示prTEV重组TEV蛋白酶的分子量为44486Da与其理论分子量44458非常接近,表明HisFF纯化后的蛋白为目标蛋白,此外,分子筛的结果显示,prTEV重组TEV蛋白酶在溶液中以单体的形式存在,大大地提高了TEV蛋白酶实际应用中的有效酶量。实验结果见图3。

2.3活性测试

使用荧光共振能量转移方法检测所述TEV蛋白酶活性,即在两个不同的荧光基团中,一个荧光基团(供体Donor)的发射光谱与另一个基团(受体Acceptor)的吸收光谱有一定的重叠,并且两个荧光基团间的距离小于

TEV蛋白酶活性测定方法具体操作如下:

将多肽底物5'-FAM-ENLYFQGSG-K(TAMRA)配制成1mM母液,分装备用。TEV蛋白酶测活缓冲液为50mM Tris-HCl(pH8.0),150mM NaCl,1mM DTT,0.5mM EDTA。用缓冲液将多肽浓度稀释成100nM,TEV蛋白酶从1μM以2倍梯度稀释,共稀释12个浓度。将30μL底物转移至384孔板中并设置两个复孔,转移30μL待测TEV蛋白酶至相应的孔板中,立即离心并振荡混匀,使用TECANF200酶标仪收集反应产生的荧光信号值。运用Graph Pad Prism9分析软件进行数据分析,最终获得待测蛋白酶的酶活参数。如图4即为Graph Pad Prism9软件分析获得不同TEV蛋白酶活参数。

2.4热稳定性测试

利用蛋白结构特点检测,蛋白具有疏水区结构并隐藏在内部,在温度上升时,蛋白的结构会被打开,暴露出疏水区,荧光染料SyproOrange就可以与该区域进行结合,并被激发荧光,根据荧光信号强度变化形成溶解曲线,溶解曲线导数最大值对应的温度即为熔点温度(Tm)。蛋白越稳定,测得的Tm值越大。

TEV蛋白酶热稳定性测定方法具体操作如下:

取5μgTEV蛋白酶加到96孔PCR板中,再加10×YPROOrange荧光染料至相应的孔中,将96孔PCR板放置qPCR仪中,设置仪器参数,按1分钟1℃的梯度从25℃升到99℃,计算蛋白的溶解曲线。如图5所示,两种蛋白酶热稳定性不同,所对应的Tm值也存在差异。

2.5进一步验证TEV蛋白酶突变体的酶切活性和稳定性

本实施例提供了一种TEV蛋白酶突变体,含有6个突变氨基酸残基,载体为pET28a,N端标签为8His-CL7-GGS,C端助溶标签为9R,命名为prTEV,氨基酸序列如SEQ ID NO:2所示。

为了研究本实施例中TEV蛋白酶突变体的酶切活性和稳定性,构建了一些对比例TEV蛋白酶突变体并将本实施例与对比例进行了比较。

其中对比例1为编号cTEV的重组TEV蛋白酶,载体为pET-28a,氨基酸序列如SEQ IDNO:4所示。

对比例2提供了一种TEV蛋白酶突变体,与本发明TEV蛋白酶突变体不同的是对比例仅突变一个位点,即将第219位氨基酸残基由丝氨酸突变为缬氨酸,载体为pET-28a,N端标签为MBP-TEV-His,C端助溶标签为9R,编号为rTEV1,氨基酸序列如SEQ ID NO:5所示。

对比例3提供了一种TEV蛋白酶突变体,与本发明TEV蛋白酶突变体不同的是对比例仅突变一个位点,即将第219位氨基酸残基由丝氨酸突变为缬氨酸,载体为pET28a,N端标签为His-GST-Thrombin,C端助溶标签为5R,编号为rTEV2,氨基酸序列如SEQ ID NO:6所示。

对比例4提供了一种TEV蛋白酶突变体,与本发明TEV蛋白酶突变体不同的是对比例仅突变一个位点,即将第219位氨基酸残基由丝氨酸突变为缬氨酸,载体为pET28a,N端标签为His,C端助溶标签为5R,编号为rTEV3,氨基酸序列如SEQ ID NO:7所示。

对比例5提供了一种TEV蛋白酶突变体,与本发明TEV蛋白酶突变体不同的是对比例仅突变一个位点,即将第219位氨基酸残基由丝氨酸突变为缬氨酸,载体为pET28a,N端标签为His-GST,C端助溶标签为5R,编号为rTEV4,氨基酸序列如SEQ ID NO:8所示。

对比例6提供了一种TEV蛋白酶突变体,与本发明TEV蛋白酶突变体不同的是对比例仅突变一个位点,即将第219位氨基酸残基由丝氨酸突变为缬氨酸,载体为pET28a,N端标签为His-CL7-GGS,C端助溶标签为5R,编号为rTEV5,氨基酸序列如SEQ ID NO:9所示。

对比例7提供了一种TEV蛋白酶突变体,与本发明TEV蛋白酶突变体不同的是其突变了两个位点,分别为第219位氨基酸残基由丝氨酸突变为缬氨酸,第153位氨基酸残基由丝氨酸突变为天冬酰胺,载体为pET28a,N端标签为His-CL7-GGS,C端助溶标签为9R,编号为rTEV6,氨基酸序列如SEQ ID NO:10所示。

对比例8提供了一种TEV蛋白酶突变体,与本发明TEV蛋白酶突变体不同的是对比例仅突变一个位点,即将第219位氨基酸残基由丝氨酸突变为缬氨酸,载体为pET28a,N端标签为His-CL7-GGS,C端助溶标签为9R,编号为rTEV7,氨基酸序列如SEQ ID NO:11所示。

对比例9提供了一种TEV蛋白酶突变体,与本发明TEV蛋白酶突变体同为六突变,不同之处是第219位氨基酸残基由丝氨酸突变为缬氨酸,载体为pET-28a,N端标签为MBP-TEV-His,C端助溶标签为5R,编号为rTEV8,氨基酸序列如SEQ ID NO:12所示。

表1 TEV蛋白酶突变体产量及热稳定性

表2 prTEV、cTEV、rTEV6、rTEV7突变位点比较

本实施例中提供的TEV蛋白酶突变体及所有对比例TEV蛋白酶突变体活性测定均在同等条件下获得。分别取相同浓度的蛋白与100nM5'-FAM-ENLYFQGSG-K(TAMRA)底物反应,使用TECANF200酶标仪监测TEV蛋白酶动力学活性。蛋白活性测定如图4所示,现有的TEV蛋白酶突变体cTEV与rTEV1蛋白酶突变体间的差异为C端助溶标签不同,结果表明C端标签为9R时,TEV蛋白酶突变体具有更高活性,故本发明优选地使用9R作为C端助溶标签。

本实施例中提供的TEV蛋白酶突变体及所有对比例TEV蛋白酶突变体产量标定均在同等条件下获得。分别取相同质量的蛋白与SYPROOrange荧光染料混匀,使用ABI7500qPCR仪,按照每分钟上升1℃的梯度从25℃升到99℃,获得溶解曲线计算蛋白Tm值。cTEV、rTEV2、rTEV3、rTEV4、rTEV5这5种TEV蛋白酶突变体的突变位点相同,C端标签均为5R,其差异为选用载体及融合标签不同。5种突变体蛋白活性测定结果如图4所示,5种TEV蛋白酶活性差异不大。各突变体的稳定性如表1所示,5种TEV蛋白酶Tm值差异不大,但从产量来看,最为突出的是rTEV5蛋白产量相较于其他高出2-4倍。故本发明优选地使用pET28a载体及His-CL7-GGS作为N端标签。

rTEV6、rTEV7及prTEV间的差异仅为突变氨基酸数目不同,即rTEV7为单突变TEV蛋白酶突变体(第219位氨基酸残基由丝氨酸突变为缬氨酸),rTEV6为双突变TEV蛋白酶突变体(第219位氨基酸残基由丝氨酸突变为缬氨酸,第153位氨基酸残基由丝氨酸突变为天冬酰胺),3种TEV蛋白酶突变体均使用pET28a载体,N端标签为His-CL7-GGS,C端助溶标签为9R。3种突变体蛋白活性测定结果如图4所示,3种突变体蛋白活性均高于现有的TEV蛋白酶突变体cTEV,其中本发明提供的六突变TEV蛋白酶prTEV活性同时高于二突变体TEV蛋白酶rTEV6和单突变体TEV蛋白酶rTEV7。对比三种突变体的Tm值,根据表1的结果可知,本发明提供的六突变TEV蛋白酶prTEV的Tm值远远高于单突变rTEV7和双突变rTEV6TEV蛋白酶,提示着prTEV具有更好的稳定性,可以在更高的温度下发挥活性。故本发明提供了一种高活性、高稳定性的TEV突变体蛋白酶。

prTEV与rTEV8均为六突变体且突变位点一致,其差异在于两者带有不同的载体和标签,本发明提供的TEV蛋白酶突变体优选地使用pET28a载体,N端以His-CL7-GGS为标签,C端添加了9R助溶标签,rTEV8使用pET28a为载体,MBP-TEV-His为N端标签,5R为C端助溶标签。2种突变体蛋白活性测定结果如图4所示,其中本发明提供的六突变TEV蛋白酶prTEV与rTEV8活性相近,但是根据表1的结果可知,本发明提供的六突变TEV蛋白酶prTEV产量比rTEV8高出3倍,Tm值高出5℃。因此认为prTEV具有更好的应用价值。

以上所述表明,本发明优选地,融合多肽标签及点突变的方法,可以在大肠杆菌异源表达系统中可以提高TEV蛋白酶的表达量和溶解性。同时这种融合标签和突变体的设计还可以大大提高TEV蛋白酶的活性和稳定性,从而使其具有更广阔的应用条件,具有更强的实际应用价值。

2.6酶切应用

为了测试prTEV的实际应用效果。用重组GST-TEV-Pro蛋白作为酶切对象,该重组蛋白N端带有TEV蛋白酶识别的TEV序列,因此TEV酶可以将该重组蛋白从TEV酶切位点切割成GST成Pro两个片段。

本实验中反应Buffer为50mMTris-HCl(pH8.0),500mMNaCl,5%glycerol。酶切反应分别在4℃和室温两种条件下进行测试。TEV蛋白酶与重组蛋白按照质量比为1:40进行孵育,分别收集1小时、2小时、4小时以及过夜不同时间点酶切后的样品进行SDS-PAGE检测,比较prTEV与cTEV的酶切效果。在4℃条件下,酶切1小时后,重组GST-TEV-Pro蛋白在两种TEV蛋白酶的作用下均有部分被切割成单独和GST和Pro片段,但是prTEV展现出更强的酶切效率。2小时、4小时,两种TEV蛋白酶的酶切效率差距更加明显。在过夜酶切后,两种TEV蛋白酶均基本将重组蛋白完全切开。实验结果见图6。

在常温下,prTEV和cTEV的酶切效果相差更加明显,在酶切2小时后,prTEV基本上将重组蛋白基本切开,而cTEV基本只切开了50%的重组蛋白。实验结果见图7。

以上所述表明,本发明优选地,融合多肽标签及点突变的方法,可以在大肠杆菌异源表达系统中可以提高TEV蛋白酶的表达量和溶解性。同时这种融合标签和突变体的设计还可以大大提高TEV蛋白酶在实际应用中的酶切效果,具有更强的实际应用价值。

以上所述实施例仅表达了本发明的几种实施方式,其描述较为具体和详细,但并不能因此而理解为对本发明专利范围的限制。应当指出的是,对于本领域的普通技术人员来说,在不脱离本发明构思的前提下,还可以做出若干变形和改进,这些都属于本发明的保护范围。

序列表

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595 600 605

Pro Val Lys Glu Ala Thr Gln Leu Met Asn Arg Arg Arg Gly Arg Arg

610 615 620

Arg Gly Arg Arg Arg Gly

625 630

<210> 6

<211> 477

<212> PRT

<213> 烟草蚀刻病毒(Tobacco etch virus)

<400> 6

Met Gly Ser Ser His His His His His His Met Ser Pro Ile Leu Gly

1 5 10 15

Tyr Trp Lys Ile Lys Gly Leu Val Gln Pro Thr Arg Leu Leu Leu Glu

20 25 30

Tyr Leu Glu Glu Lys Tyr Glu Glu His Leu Tyr Glu Arg Asp Glu Gly

35 40 45

Asp Lys Trp Arg Asn Lys Lys Phe Glu Leu Gly Leu Glu Phe Pro Asn

50 55 60

Leu Pro Tyr Tyr Ile Asp Gly Asp Val Lys Leu Thr Gln Ser Met Ala

65 70 75 80

Ile Ile Arg Tyr Ile Ala Asp Lys His Asn Met Leu Gly Gly Cys Pro

85 90 95

Lys Glu Arg Ala Glu Ile Ser Met Leu Glu Gly Ala Val Leu Asp Ile

100 105 110

Arg Tyr Gly Val Ser Arg Ile Ala Tyr Ser Lys Asp Phe Glu Thr Leu

115 120 125

Lys Val Asp Phe Leu Ser Lys Leu Pro Glu Met Leu Lys Met Phe Glu

130 135 140

Asp Arg Leu Cys His Lys Thr Tyr Leu Asn Gly Asp His Val Thr His

145 150 155 160

Pro Asp Phe Met Leu Tyr Asp Ala Leu Asp Val Val Leu Tyr Met Asp

165 170 175

Pro Met Cys Leu Asp Ala Phe Pro Lys Leu Val Cys Phe Lys Lys Arg

180 185 190

Ile Glu Ala Ile Pro Gln Ile Asp Lys Tyr Leu Lys Ser Ser Lys Tyr

195 200 205

Ile Ala Trp Pro Leu Gln Gly Trp Gln Ala Thr Phe Gly Gly Gly Asp

210 215 220

His Pro Pro Lys Ser Asp Leu Val Pro Arg Gly Ser Gly Glu Ser Leu

225 230 235 240

Phe Lys Gly Pro Arg Asp Tyr Asn Pro Ile Ser Ser Thr Ile Cys His

245 250 255

Leu Thr Asn Glu Ser Asp Gly His Thr Thr Ser Leu Tyr Gly Ile Gly

260 265 270

Phe Gly Pro Phe Ile Ile Thr Asn Lys His Leu Phe Arg Arg Asn Asn

275 280 285

Gly Thr Leu Leu Val Gln Ser Leu His Gly Val Phe Lys Val Lys Asn

290 295 300

Thr Thr Thr Leu Gln Gln His Leu Ile Asp Gly Arg Asp Met Ile Ile

305 310 315 320

Ile Arg Met Pro Lys Asp Phe Pro Pro Phe Pro Gln Lys Leu Lys Phe

325 330 335

Arg Glu Pro Gln Arg Glu Glu Arg Ile Cys Leu Val Thr Thr Asn Phe

340 345 350

Gln Thr Lys Ser Met Ser Ser Met Val Ser Asp Thr Ser Cys Thr Phe

355 360 365

Pro Ser Ser Asp Gly Ile Phe Trp Lys His Trp Ile Gln Thr Lys Asp

370 375 380

Gly Gln Cys Gly Ser Pro Leu Val Ser Thr Arg Asp Gly Phe Ile Val

385 390 395 400

Gly Ile His Ser Ala Ser Asn Phe Thr Asn Thr Asn Asn Tyr Phe Thr

405 410 415

Ser Val Pro Lys Asn Phe Met Glu Leu Leu Thr Asn Gln Glu Ala Gln

420 425 430

Gln Trp Val Ser Gly Trp Arg Leu Asn Ala Asp Ser Val Leu Trp Gly

435 440 445

Gly His Lys Val Phe Met Val Lys Pro Glu Glu Pro Phe Gln Pro Val

450 455 460

Lys Glu Ala Thr Gln Leu Met Asn Arg Arg Arg Arg Arg

465 470 475

<210> 7

<211> 251

<212> PRT

<213> 烟草蚀刻病毒(Tobacco etch virus)

<400> 7

Met Gly Ser Ser His His His His His His Gly Glu Ser Leu Phe Lys

1 5 10 15

Gly Pro Arg Asp Tyr Asn Pro Ile Ser Ser Thr Ile Cys His Leu Thr

20 25 30

Asn Glu Ser Asp Gly His Thr Thr Ser Leu Tyr Gly Ile Gly Phe Gly

35 40 45

Pro Phe Ile Ile Thr Asn Lys His Leu Phe Arg Arg Asn Asn Gly Thr

50 55 60

Leu Leu Val Gln Ser Leu His Gly Val Phe Lys Val Lys Asn Thr Thr

65 70 75 80

Thr Leu Gln Gln His Leu Ile Asp Gly Arg Asp Met Ile Ile Ile Arg

85 90 95

Met Pro Lys Asp Phe Pro Pro Phe Pro Gln Lys Leu Lys Phe Arg Glu

100 105 110

Pro Gln Arg Glu Glu Arg Ile Cys Leu Val Thr Thr Asn Phe Gln Thr

115 120 125

Lys Ser Met Ser Ser Met Val Ser Asp Thr Ser Cys Thr Phe Pro Ser

130 135 140

Ser Asp Gly Ile Phe Trp Lys His Trp Ile Gln Thr Lys Asp Gly Gln

145 150 155 160

Cys Gly Ser Pro Leu Val Ser Thr Arg Asp Gly Phe Ile Val Gly Ile

165 170 175

His Ser Ala Ser Asn Phe Thr Asn Thr Asn Asn Tyr Phe Thr Ser Val

180 185 190

Pro Lys Asn Phe Met Glu Leu Leu Thr Asn Gln Glu Ala Gln Gln Trp

195 200 205

Val Ser Gly Trp Arg Leu Asn Ala Asp Ser Val Leu Trp Gly Gly His

210 215 220

Lys Val Phe Met Val Lys Pro Glu Glu Pro Phe Gln Pro Val Lys Glu

225 230 235 240

Ala Thr Gln Leu Met Asn Arg Arg Arg Arg Arg

245 250

<210> 8

<211> 468

<212> PRT

<213> 烟草蚀刻病毒(Tobacco etch virus)

<400> 8

Met Gly His His His His His His Ser Pro Ile Leu Gly Tyr Trp Lys

1 5 10 15

Ile Lys Gly Leu Val Gln Pro Thr Arg Leu Leu Leu Glu Tyr Leu Glu

20 25 30

Glu Lys Tyr Glu Glu His Leu Tyr Glu Arg Asp Glu Gly Asp Lys Trp

35 40 45

Arg Asn Lys Lys Phe Glu Leu Gly Leu Glu Phe Pro Asn Leu Pro Tyr

50 55 60

Tyr Ile Asp Gly Asp Val Lys Leu Thr Gln Ser Met Ala Ile Ile Arg

65 70 75 80

Tyr Ile Ala Asp Lys His Asn Met Leu Gly Gly Cys Pro Lys Glu Arg

85 90 95

Ala Glu Ile Ser Met Leu Glu Gly Ala Val Leu Asp Ile Arg Tyr Gly

100 105 110

Val Ser Arg Ile Ala Tyr Ser Lys Asp Phe Glu Thr Leu Lys Val Asp

115 120 125

Phe Leu Ser Lys Leu Pro Glu Met Leu Lys Met Phe Glu Asp Arg Leu

130 135 140

Cys His Lys Thr Tyr Leu Asn Gly Asp His Val Thr His Pro Asp Phe

145 150 155 160

Met Leu Tyr Asp Ala Leu Asp Val Val Leu Tyr Met Asp Pro Met Cys

165 170 175

Leu Asp Ala Phe Pro Lys Leu Val Cys Phe Lys Lys Arg Ile Glu Ala

180 185 190

Ile Pro Gln Ile Asp Lys Tyr Leu Lys Ser Ser Lys Tyr Ile Ala Trp

195 200 205

Pro Leu Gln Gly Trp Gln Ala Thr Phe Gly Gly Gly Asp His Pro Pro

210 215 220

Lys Ser Asp Gly Glu Ser Leu Phe Lys Gly Pro Arg Asp Tyr Asn Pro

225 230 235 240

Ile Ser Ser Thr Ile Cys His Leu Thr Asn Glu Ser Asp Gly His Thr

245 250 255

Thr Ser Leu Tyr Gly Ile Gly Phe Gly Pro Phe Ile Ile Thr Asn Lys

260 265 270

His Leu Phe Arg Arg Asn Asn Gly Thr Leu Leu Val Gln Ser Leu His

275 280 285

Gly Val Phe Lys Val Lys Asn Thr Thr Thr Leu Gln Gln His Leu Ile

290 295 300

Asp Gly Arg Asp Met Ile Ile Ile Arg Met Pro Lys Asp Phe Pro Pro

305 310 315 320

Phe Pro Gln Lys Leu Lys Phe Arg Glu Pro Gln Arg Glu Glu Arg Ile

325 330 335

Cys Leu Val Thr Thr Asn Phe Gln Thr Lys Ser Met Ser Ser Met Val

340 345 350

Ser Asp Thr Ser Cys Thr Phe Pro Ser Ser Asp Gly Ile Phe Trp Lys

355 360 365

His Trp Ile Gln Thr Lys Asp Gly Gln Cys Gly Ser Pro Leu Val Ser

370 375 380

Thr Arg Asp Gly Phe Ile Val Gly Ile His Ser Ala Ser Asn Phe Thr

385 390 395 400

Asn Thr Asn Asn Tyr Phe Thr Ser Val Pro Lys Asn Phe Met Glu Leu

405 410 415

Leu Thr Asn Gln Glu Ala Gln Gln Trp Val Ser Gly Trp Arg Leu Asn

420 425 430

Ala Asp Ser Val Leu Trp Gly Gly His Lys Val Phe Met Val Lys Pro

435 440 445

Glu Glu Pro Phe Gln Pro Val Lys Glu Ala Thr Gln Leu Met Asn Arg

450 455 460

Arg Arg Arg Arg

465

<210> 9

<211> 381

<212> PRT

<213> 烟草蚀刻病毒(Tobacco etch virus)

<400> 9

Met His His His His His His Ser Lys Ser Asn Glu Pro Gly Lys Ala

1 5 10 15

Thr Gly Glu Gly Lys Pro Val Asn Asn Lys Trp Leu Asn Asn Ala Gly

20 25 30

Lys Asp Leu Gly Ser Pro Val Pro Asp Arg Ile Ala Asn Lys Leu Arg

35 40 45

Asp Lys Glu Phe Glu Ser Phe Asp Asp Phe Arg Glu Thr Phe Trp Glu

50 55 60

Glu Val Ser Lys Asp Pro Glu Leu Ser Lys Gln Phe Ser Arg Asn Asn

65 70 75 80

Asn Asp Arg Met Lys Val Gly Lys Ala Pro Lys Thr Arg Thr Gln Asp

85 90 95

Val Ser Gly Lys Arg Thr Ser Phe Glu Leu Asn His Gln Lys Pro Ile

100 105 110

Glu Gln Asn Gly Gly Val Tyr Asp Met Asp Asn Ile Ser Val Val Thr

115 120 125

Pro Lys Arg Asn Ile Asp Ile Glu Gly Gly Gly Ser Gly Glu Ser Leu

130 135 140

Phe Lys Gly Pro Arg Asp Tyr Asn Pro Ile Ser Ser Thr Ile Cys His

145 150 155 160

Leu Thr Asn Glu Ser Asp Gly His Thr Thr Ser Leu Tyr Gly Ile Gly

165 170 175

Phe Gly Pro Phe Ile Ile Thr Asn Lys His Leu Phe Arg Arg Asn Asn

180 185 190

Gly Thr Leu Leu Val Gln Ser Leu His Gly Val Phe Lys Val Lys Asn

195 200 205

Thr Thr Thr Leu Gln Gln His Leu Ile Asp Gly Arg Asp Met Ile Ile

210 215 220

Ile Arg Met Pro Lys Asp Phe Pro Pro Phe Pro Gln Lys Leu Lys Phe

225 230 235 240

Arg Glu Pro Gln Arg Glu Glu Arg Ile Cys Leu Val Thr Thr Asn Phe

245 250 255

Gln Thr Lys Ser Met Ser Ser Met Val Ser Asp Thr Ser Cys Thr Phe

260 265 270

Pro Ser Ser Asp Gly Ile Phe Trp Lys His Trp Ile Gln Thr Lys Asp

275 280 285

Gly Gln Cys Gly Ser Pro Leu Val Ser Thr Arg Asp Gly Phe Ile Val

290 295 300

Gly Ile His Ser Ala Ser Asn Phe Thr Asn Thr Asn Asn Tyr Phe Thr

305 310 315 320

Ser Val Pro Lys Asn Phe Met Glu Leu Leu Thr Asn Gln Glu Ala Gln

325 330 335

Gln Trp Val Ser Gly Trp Arg Leu Asn Ala Asp Ser Val Leu Trp Gly

340 345 350

Gly His Lys Val Phe Met Val Lys Pro Glu Glu Pro Phe Gln Pro Val

355 360 365

Lys Glu Ala Thr Gln Leu Met Asn Arg Arg Arg Arg Arg

370 375 380

<210> 10

<211> 388

<212> PRT

<213> 烟草蚀刻病毒(Tobacco etch virus)

<400> 10

Met His His His His His His Ser Lys Ser Asn Glu Pro Gly Lys Ala

1 5 10 15

Thr Gly Glu Gly Lys Pro Val Asn Asn Lys Trp Leu Asn Asn Ala Gly

20 25 30

Lys Asp Leu Gly Ser Pro Val Pro Asp Arg Ile Ala Asn Lys Leu Arg

35 40 45

Asp Lys Glu Phe Glu Ser Phe Asp Asp Phe Arg Glu Thr Phe Trp Glu

50 55 60

Glu Val Ser Lys Asp Pro Glu Leu Ser Lys Gln Phe Ser Arg Asn Asn

65 70 75 80

Asn Asp Arg Met Lys Val Gly Lys Ala Pro Lys Thr Arg Thr Gln Asp

85 90 95

Val Ser Gly Lys Arg Thr Ser Phe Glu Leu Asn His Gln Lys Pro Ile

100 105 110

Glu Gln Asn Gly Gly Val Tyr Asp Met Asp Asn Ile Ser Val Val Thr

115 120 125

Pro Lys Arg Asn Ile Asp Ile Glu Gly Gly Gly Ser Gly Glu Ser Leu

130 135 140

Phe Lys Gly Pro Arg Asp Tyr Asn Pro Ile Ser Ser Thr Ile Cys His

145 150 155 160

Leu Thr Asn Glu Ser Asp Gly His Thr Thr Ser Leu Tyr Gly Ile Gly

165 170 175

Phe Gly Pro Phe Ile Ile Thr Asn Lys His Leu Phe Arg Arg Asn Asn

180 185 190

Gly Thr Leu Leu Val Gln Ser Leu His Gly Val Phe Lys Val Lys Asn

195 200 205

Thr Thr Thr Leu Gln Gln His Leu Ile Asp Gly Arg Asp Met Ile Ile

210 215 220

Ile Arg Met Pro Lys Asp Phe Pro Pro Phe Pro Gln Lys Leu Lys Phe

225 230 235 240

Arg Glu Pro Gln Arg Glu Glu Arg Ile Cys Leu Val Thr Thr Asn Phe

245 250 255

Gln Thr Lys Ser Met Ser Ser Met Val Ser Asp Thr Ser Cys Thr Phe

260 265 270

Pro Ser Ser Asp Gly Ile Phe Trp Lys His Trp Ile Gln Thr Lys Asp

275 280 285

Gly Gln Cys Gly Asn Pro Leu Val Ser Thr Arg Asp Gly Phe Ile Val

290 295 300

Gly Ile His Ser Ala Ser Asn Phe Thr Asn Thr Asn Asn Tyr Phe Thr

305 310 315 320

Ser Val Pro Lys Asn Phe Met Glu Leu Leu Thr Asn Gln Glu Ala Gln

325 330 335

Gln Trp Val Ser Gly Trp Arg Leu Asn Ala Asp Ser Val Leu Trp Gly

340 345 350

Gly His Lys Val Phe Met Val Lys Pro Glu Glu Pro Phe Gln Pro Val

355 360 365

Lys Glu Ala Thr Gln Leu Met Asn Arg Arg Arg Gly Arg Arg Arg Gly

370 375 380

Arg Arg Arg Gly

385

<210> 11

<211> 388

<212> PRT

<213> 烟草蚀刻病毒(Tobacco etch virus)

<400> 11

Met His His His His His His Ser Lys Ser Asn Glu Pro Gly Lys Ala

1 5 10 15

Thr Gly Glu Gly Lys Pro Val Asn Asn Lys Trp Leu Asn Asn Ala Gly

20 25 30

Lys Asp Leu Gly Ser Pro Val Pro Asp Arg Ile Ala Asn Lys Leu Arg

35 40 45

Asp Lys Glu Phe Glu Ser Phe Asp Asp Phe Arg Glu Thr Phe Trp Glu

50 55 60

Glu Val Ser Lys Asp Pro Glu Leu Ser Lys Gln Phe Ser Arg Asn Asn

65 70 75 80

Asn Asp Arg Met Lys Val Gly Lys Ala Pro Lys Thr Arg Thr Gln Asp

85 90 95

Val Ser Gly Lys Arg Thr Ser Phe Glu Leu Asn His Gln Lys Pro Ile

100 105 110

Glu Gln Asn Gly Gly Val Tyr Asp Met Asp Asn Ile Ser Val Val Thr

115 120 125

Pro Lys Arg Asn Ile Asp Ile Glu Gly Gly Gly Ser Gly Glu Ser Leu

130 135 140

Phe Lys Gly Pro Arg Asp Tyr Asn Pro Ile Ser Ser Thr Ile Cys His

145 150 155 160

Leu Thr Asn Glu Ser Asp Gly His Thr Thr Ser Leu Tyr Gly Ile Gly

165 170 175

Phe Gly Pro Phe Ile Ile Thr Asn Lys His Leu Phe Arg Arg Asn Asn

180 185 190

Gly Thr Leu Leu Val Gln Ser Leu His Gly Val Phe Lys Val Lys Asn

195 200 205

Thr Thr Thr Leu Gln Gln His Leu Ile Asp Gly Arg Asp Met Ile Ile

210 215 220

Ile Arg Met Pro Lys Asp Phe Pro Pro Phe Pro Gln Lys Leu Lys Phe

225 230 235 240

Arg Glu Pro Gln Arg Glu Glu Arg Ile Cys Leu Val Thr Thr Asn Phe

245 250 255

Gln Thr Lys Ser Met Ser Ser Met Val Ser Asp Thr Ser Cys Thr Phe

260 265 270

Pro Ser Ser Asp Gly Ile Phe Trp Lys His Trp Ile Gln Thr Lys Asp

275 280 285

Gly Gln Cys Gly Ser Pro Leu Val Ser Thr Arg Asp Gly Phe Ile Val

290 295 300

Gly Ile His Ser Ala Ser Asn Phe Thr Asn Thr Asn Asn Tyr Phe Thr

305 310 315 320

Ser Val Pro Lys Asn Phe Met Glu Leu Leu Thr Asn Gln Glu Ala Gln

325 330 335

Gln Trp Val Ser Gly Trp Arg Leu Asn Ala Asp Ser Val Leu Trp Gly

340 345 350

Gly His Lys Val Phe Met Val Lys Pro Glu Glu Pro Phe Gln Pro Val

355 360 365

Lys Glu Ala Thr Gln Leu Met Asn Arg Arg Arg Gly Arg Arg Arg Gly

370 375 380

Arg Arg Arg Gly

385

<210> 12

<211> 617

<212> PRT

<213> 烟草蚀刻病毒(Tobacco etch virus)

<400> 12

Met Gly Lys Ile Glu Glu Gly Lys Leu Val Ile Trp Ile Asn Gly Asp

1 5 10 15

Lys Gly Tyr Asn Gly Leu Ala Glu Val Gly Lys Lys Phe Glu Lys Asp

20 25 30

Thr Gly Ile Lys Val Thr Val Glu His Pro Asp Lys Leu Glu Glu Lys

35 40 45

Phe Pro Gln Val Ala Ala Thr Gly Asp Gly Pro Asp Ile Ile Phe Trp

50 55 60

Ala His Asp Arg Phe Gly Gly Tyr Ala Gln Ser Gly Leu Leu Ala Glu

65 70 75 80

Ile Thr Pro Asp Lys Ala Phe Gln Asp Lys Leu Tyr Pro Phe Thr Trp

85 90 95

Asp Ala Val Arg Tyr Asn Gly Lys Leu Ile Ala Tyr Pro Ile Ala Val

100 105 110

Glu Ala Leu Ser Leu Ile Tyr Asn Lys Asp Leu Leu Pro Asn Pro Pro

115 120 125

Lys Thr Trp Glu Glu Ile Pro Ala Leu Asp Lys Glu Leu Lys Ala Lys

130 135 140

Gly Lys Ser Ala Leu Met Phe Asn Leu Gln Glu Pro Tyr Phe Thr Trp

145 150 155 160

Pro Leu Ile Ala Ala Asp Gly Gly Tyr Ala Phe Lys Tyr Glu Asn Gly

165 170 175

Lys Tyr Asp Ile Lys Asp Val Gly Val Asp Asn Ala Gly Ala Lys Ala

180 185 190

Gly Leu Thr Phe Leu Val Asp Leu Ile Lys Asn Lys His Met Asn Ala

195 200 205

Asp Thr Asp Tyr Ser Ile Ala Glu Ala Ala Phe Asn Lys Gly Glu Thr

210 215 220

Ala Met Thr Ile Asn Gly Pro Trp Ala Trp Ser Asn Ile Asp Thr Ser

225 230 235 240

Lys Val Asn Tyr Gly Val Thr Val Leu Pro Thr Phe Lys Gly Gln Pro

245 250 255

Ser Lys Pro Phe Val Gly Val Leu Ser Ala Gly Ile Asn Ala Ala Ser

260 265 270

Pro Asn Lys Glu Leu Ala Lys Glu Phe Leu Glu Asn Tyr Leu Leu Thr

275 280 285

Asp Glu Gly Leu Glu Ala Val Asn Lys Asp Lys Pro Leu Gly Ala Val

290 295 300

Ala Leu Lys Ser Tyr Glu Glu Glu Leu Ala Lys Asp Pro Arg Ile Ala

305 310 315 320

Ala Thr Met Glu Asn Ala Gln Lys Gly Glu Ile Met Pro Asn Ile Pro

325 330 335

Gln Met Ser Ala Phe Trp Tyr Ala Val Arg Thr Ala Val Ile Asn Ala

340 345 350

Ala Ser Gly Arg Gln Thr Val Asp Glu Ala Leu Lys Asp Ala Gln Thr

355 360 365

Asn Ser Gly Ser Gly Gly Ser Gly Gly Glu Ser Leu Phe Lys Gly Pro

370 375 380

Arg Asp Tyr Asn Pro Ile Ser Ser Ser Ile Cys His Leu Thr Asn Glu

385 390 395 400

Ser Asp Gly His Thr Thr Ser Leu Tyr Gly Ile Gly Phe Gly Pro Phe

405 410 415

Ile Ile Thr Asn Lys His Leu Phe Arg Arg Asn Asn Gly Thr Leu Val

420 425 430

Val Gln Ser Leu His Gly Val Phe Lys Val Lys Asp Thr Thr Thr Leu

435 440 445

Gln Gln His Leu Val Asp Gly Arg Asp Met Ile Ile Ile Arg Met Pro

450 455 460

Lys Asp Phe Pro Pro Phe Pro Gln Lys Leu Lys Phe Arg Glu Pro Gln

465 470 475 480

Arg Glu Glu Arg Ile Cys Leu Val Thr Thr Asn Phe Gln Thr Lys Ser

485 490 495

Met Ser Ser Met Val Ser Asp Thr Ser Cys Thr Phe Pro Ser Gly Asp

500 505 510

Gly Ile Phe Trp Lys His Trp Ile Gln Thr Lys Asp Gly Gln Cys Gly

515 520 525

Ser Pro Leu Val Ser Thr Arg Asp Gly Phe Ile Val Gly Ile His Ser

530 535 540

Ala Ser Asn Phe Thr Asn Thr Asn Asn Tyr Phe Thr Ser Val Pro Lys

545 550 555 560

Asn Phe Met Glu Leu Leu Thr Asn Gln Glu Ala Gln Gln Trp Val Ser

565 570 575

Gly Trp Arg Leu Asn Ala Asp Ser Val Leu Trp Gly Gly His Lys Val

580 585 590

Phe Met Val Lys Pro Glu Glu Pro Phe Gln Pro Val Lys Glu Ala Thr

595 600 605

Gln Leu Met Asn Arg Arg Arg Arg Arg

610 615

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