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    • 3. 发明申请
    • METHODS FOR PRODUCTION OF PROTEINS
    • 生产蛋白质的方法
    • US20110108420A1
    • 2011-05-12
    • US13006354
    • 2011-01-13
    • DEB K. CHATTERJEEMary LongoElizabeth FlynnRobert Oberfelder
    • DEB K. CHATTERJEEMary LongoElizabeth FlynnRobert Oberfelder
    • B01D57/02C07K14/195C12N9/96C07K14/435C07K14/57C07K14/245
    • C07K1/26C07K1/1077C07K1/13C07K14/001C07K2319/00C07K2319/01C12N9/0036C12P21/02Y02P20/52
    • The current invention provides methods for producing a polypeptide as inclusion bodies in bacterial host cells. The present methods are carried out by forming a gene construct comprising the genetic sequence encoding a polypeptide operatively linked to that of an inclusion partner protein, such as E. coli thioredoxin or a modified E. coli thioredoxin, such that host cells comprising the gene construct produce the polypeptide as intracellular inclusion bodies. The methods of the present invention facilitate the rapid isolation and purification of recombinant proteins. In addition, the present methods may be useful for producing polypeptides or proteins which are small and are typically difficult to express, as well as those proteins that are toxic to host cells such as E. coli. The present invention also provides plasmids, vectors and host cells to be used in the present invention for production of polypeptides, and methods of production of polypeptides using these vectors and host cells. The invention further provides methods for producing protein molecular weight ladders for use in protein gel electrophoresis, as well as proteins and protein molecular weight ladders produced by these methods.
    • 本发明提供了在细菌宿主细胞中产生作为包涵体的多肽的方法。 本发明的方法通过形成包含编码与包含配对蛋白例如大肠杆菌硫氧还蛋白或修饰的大肠杆菌硫氧还蛋白的内含子配偶体蛋白可操作地连接的多肽的遗传序列来进行,使得包含该基因构建体的宿主细胞 产生多肽作为细胞内包涵体。 本发明的方法促进重组蛋白的快速分离和纯化。 此外,本发明的方法可用于生产小而通常难以表达的多肽或蛋白质,以及对宿主细胞如大肠杆菌毒性的那些蛋白质。 本发明还提供了用于本发明中用于产生多肽的质粒,载体和宿主细胞,以及使用这些载体和宿主细胞产生多肽的方法。 本发明进一步提供了用于蛋白质凝胶电泳的蛋白质分子级梯子的制备方法,以及通过这些方法制备的蛋白质和蛋白质分子级梯子。
    • 4. 发明授权
    • Methods for production of proteins
    • 生产蛋白质的方法
    • US08012715B2
    • 2011-09-06
    • US11618723
    • 2006-12-29
    • Deb K. ChatterjeeMary LongoElizabeth FlynnRobert Oberfelder
    • Deb K. ChatterjeeMary LongoElizabeth FlynnRobert Oberfelder
    • C07K1/00C12P21/04
    • C07K1/26C07K1/1077C07K1/13C07K14/001C07K2319/00C07K2319/01C12N9/0036C12P21/02Y02P20/52
    • The current invention provides methods for producing a polypeptide as inclusion bodies in bacterial host cells. The present methods are carried out by forming a gene construct comprising the genetic sequence encoding a polypeptide operatively linked to that of an inclusion partner protein, such as E. coli thioredoxin or a modified E. coli thioredoxin, such that host cells comprising the gene construct produce the polypeptide as intracellular inclusion bodies. The methods of the present invention facilitate the rapid isolation and purification of recombinant proteins. In addition, the present methods may be useful for producing polypeptides or proteins which are small and are typically difficult to express, as well as those proteins that are toxic to host cells such as E. coli. The present invention also provides plasmids, vectors and host cells to be used in the present invention for production of polypeptides, and methods of production of polypeptides using these vectors and host cells. The invention further provides methods for producing protein molecular weight ladders for use in protein gel electrophoresis, as well as proteins and protein molecular weight ladders produced by these methods.
    • 本发明提供了在细菌宿主细胞中产生作为包涵体的多肽的方法。 本发明的方法通过形成包含编码与包含配对蛋白例如大肠杆菌硫氧还蛋白或修饰的大肠杆菌硫氧还蛋白的内含子配偶体蛋白可操作地连接的多肽的遗传序列来进行,使得包含该基因构建体的宿主细胞 产生多肽作为细胞内包涵体。 本发明的方法促进重组蛋白的快速分离和纯化。 此外,本发明的方法可用于生产小而通常难以表达的多肽或蛋白质,以及对宿主细胞如大肠杆菌毒性的那些蛋白质。 本发明还提供了用于本发明中用于产生多肽的质粒,载体和宿主细胞,以及使用这些载体和宿主细胞产生多肽的方法。 本发明进一步提供了用于蛋白质凝胶电泳的蛋白质分子级梯子的制备方法,以及通过这些方法制备的蛋白质和蛋白质分子级梯子。
    • 5. 发明授权
    • Methods for production of proteins
    • 生产蛋白质的方法
    • US08519099B2
    • 2013-08-27
    • US13006354
    • 2011-01-13
    • Deb ChatterjeeMary LongoElizabeth FlynnRobert Oberfelder
    • Deb ChatterjeeMary LongoElizabeth FlynnRobert Oberfelder
    • C07K1/00
    • C07K1/26C07K1/1077C07K1/13C07K14/001C07K2319/00C07K2319/01C12N9/0036C12P21/02Y02P20/52
    • The current invention provides methods for producing a polypeptide as inclusion bodies in bacterial host cells. The present methods are carried out by forming a gene construct comprising the genetic sequence encoding a polypeptide operatively linked to that of an inclusion partner protein, such as E. coli thioredoxin or a modified E. coli thioredoxin, such that host cells comprising the gene construct produce the polypeptide as intracellular inclusion bodies. The methods of the present invention facilitate the rapid isolation and purification of recombinant proteins. In addition, the present methods may be useful for producing polypeptides or proteins which are small and are typically difficult to express, as well as those proteins that are toxic to host cells such as E. coli. The present invention also provides plasmids, vectors and host cells to be used in the present invention for production of polypeptides, and methods of production of polypeptides using these vectors and host cells. The invention further provides methods for producing protein molecular weight ladders for use in protein gel electrophoresis, as well as proteins and protein molecular weight ladders produced by these methods.
    • 本发明提供了在细菌宿主细胞中产生作为包涵体的多肽的方法。 本发明的方法通过形成包含编码与包含配对蛋白例如大肠杆菌硫氧还蛋白或修饰的大肠杆菌硫氧还蛋白的内含子配偶体蛋白可操作地连接的多肽的遗传序列来进行,使得包含该基因构建体的宿主细胞 产生多肽作为细胞内包涵体。 本发明的方法促进重组蛋白的快速分离和纯化。 此外,本发明的方法可用于生产小而通常难以表达的多肽或蛋白质,以及对宿主细胞如大肠杆菌毒性的那些蛋白质。 本发明还提供了用于本发明中用于产生多肽的质粒,载体和宿主细胞,以及使用这些载体和宿主细胞产生多肽的方法。 本发明进一步提供了用于蛋白质凝胶电泳的蛋白质分子级梯子的制备方法,以及通过这些方法制备的蛋白质和蛋白质分子级梯子。
    • 7. 发明申请
    • Methods of production of proteins
    • 蛋白质生产方法
    • US20060269992A1
    • 2006-11-30
    • US11329418
    • 2006-01-11
    • Deb ChatterjeeMary LongoElizabeth FlynnRobert Oberfelder
    • Deb ChatterjeeMary LongoElizabeth FlynnRobert Oberfelder
    • C12P21/06C07K14/47
    • C07K1/26C07K1/1077C07K1/13C07K14/001C07K2319/00C07K2319/01C12N9/0036C12P21/02Y02P20/52
    • The current invention provides methods for producing a polypeptide as inclusion bodies in bacterial host cells. The present methods are carried out by forming a gene construct comprising the genetic sequence encoding a polypeptide operatively linked to that of an inclusion partner protein, such as E. coli thioredoxin or a modified E. coli thioredoxin, such that host cells comprising the gene construct produce the polypeptide as intracellular inclusion bodies. The methods of the present invention facilitate the rapid isolation and purification of recombinant proteins. In addition, the present methods may be useful for producing polypeptides or proteins which are small and are typically difficult to express, as well as those proteins that are toxic to host cells such as E. coli. The present invention also provides plasmids, vectors and host cells to be used in the present invention for production of polypeptides, and methods of production of polypeptides using these vectors and host cells. The invention further provides methods for producing protein molecular weight ladders for use in protein gel electrophoresis, as well as proteins and protein molecular weight ladders produced by these methods.
    • 本发明提供了在细菌宿主细胞中产生作为包涵体的多肽的方法。 本发明的方法通过形成包含编码与包含配对蛋白例如大肠杆菌硫氧还蛋白或修饰的大肠杆菌硫氧还蛋白的内含子配偶体蛋白可操作地连接的多肽的遗传序列来进行,使得包含该基因构建体的宿主细胞 产生多肽作为细胞内包涵体。 本发明的方法促进重组蛋白的快速分离和纯化。 此外,本发明的方法可用于生产小而通常难以表达的多肽或蛋白质,以及对宿主细胞如大肠杆菌毒性的那些蛋白质。 本发明还提供了用于本发明中用于产生多肽的质粒,载体和宿主细胞,以及使用这些载体和宿主细胞产生多肽的方法。 本发明进一步提供了用于蛋白质凝胶电泳的蛋白质分子级梯子的制备方法,以及通过这些方法制备的蛋白质和蛋白质分子级梯子。
    • 9. 发明申请
    • Methods for Production of Proteins
    • 蛋白质生产方法
    • US20070190606A1
    • 2007-08-16
    • US11618723
    • 2006-12-29
    • Deb ChatterjeeMary LongoElizabeth FlynnRobert Oberfelder
    • Deb ChatterjeeMary LongoElizabeth FlynnRobert Oberfelder
    • C12P21/06C12N9/02C07H21/04C12N1/21C12N15/74
    • C07K1/26C07K1/1077C07K1/13C07K14/001C07K2319/00C07K2319/01C12N9/0036C12P21/02Y02P20/52
    • The current invention provides methods for producing a polypeptide as inclusion bodies in bacterial host cells. The present methods are carried out by forming a gene construct comprising the genetic sequence encoding a polypeptide operatively linked to that of an inclusion partner protein, such as E. coli thioredoxin or a modified E. coli thioredoxin, such that host cells comprising the gene construct produce the polypeptide as intracellular inclusion bodies. The methods of the present invention facilitate the rapid isolation and purification of recombinant proteins. In addition, the present methods may be useful for producing polypeptides or proteins which are small and are typically difficult to express, as well as those proteins that are toxic to host cells such as E. coli. The present invention also provides plasmids, vectors and host cells to be used in the present invention for production of polypeptides, and methods of production of polypeptides using these vectors and host cells. The invention further provides methods for producing protein molecular weight ladders for use in protein gel electrophoresis, as well as proteins and protein molecular weight ladders produced by these methods.
    • 本发明提供了在细菌宿主细胞中产生作为包涵体的多肽的方法。 本发明的方法通过形成包含编码与包含配对蛋白例如大肠杆菌硫氧还蛋白或修饰的大肠杆菌硫氧还蛋白的内含子配偶体蛋白可操作地连接的多肽的遗传序列来进行,使得包含该基因构建体的宿主细胞 产生多肽作为细胞内包涵体。 本发明的方法促进重组蛋白的快速分离和纯化。 此外,本发明的方法可用于生产小而通常难以表达的多肽或蛋白质,以及对宿主细胞如大肠杆菌毒性的那些蛋白质。 本发明还提供了用于本发明中用于产生多肽的质粒,载体和宿主细胞,以及使用这些载体和宿主细胞产生多肽的方法。 本发明进一步提供了用于蛋白质凝胶电泳的蛋白质分子梯度的制备方法,以及通过这些方法制备的蛋白质和蛋白质分子量梯。
    • 10. 发明授权
    • Methods of production of proteins
    • 蛋白质生产方法
    • US07265206B2
    • 2007-09-04
    • US11329418
    • 2006-01-11
    • Deb K. ChatterjeeMary C. LongoElizabeth FlynnRobert W. Oberfelder
    • Deb K. ChatterjeeMary C. LongoElizabeth FlynnRobert W. Oberfelder
    • C07K1/00C12P21/06C12P21/04
    • C07K1/26C07K1/1077C07K1/13C07K14/001C07K2319/00C07K2319/01C12N9/0036C12P21/02Y02P20/52
    • The current invention provides methods for producing a polypeptide as inclusion bodies in bacterial host cells. The present methods are carried out by forming a gene construct comprising the genetic sequence encoding a polypeptide operatively linked to that of an inclusion partner protein, such as E. coli thioredoxin or a modified E. coli thioredoxin, such that host cells comprising the gene construct produce the polypeptide as intracellular inclusion bodies. The methods of the present invention facilitate the rapid isolation and purification of recombinant proteins. In addition, the present methods may be useful for producing polypeptides or proteins which are small and are typically difficult to express, as well as those proteins that are toxic to host cells such as E. coli. The present invention also provides plasmids, vectors and host cells to be used in the present invention for production of polypeptides, and methods of production of polypeptides using these vectors and host cells. The invention further provides methods for producing protein molecular weight ladders for use in protein gel electrophoresis, as well as proteins and protein molecular weight ladders produced by these methods.
    • 本发明提供了在细菌宿主细胞中产生作为包涵体的多肽的方法。 本发明的方法通过形成包含编码与包含配对蛋白例如大肠杆菌硫氧还蛋白或修饰的大肠杆菌硫氧还蛋白的内含子配偶体蛋白可操作地连接的多肽的遗传序列来进行,使得包含该基因构建体的宿主细胞 产生多肽作为细胞内包涵体。 本发明的方法促进重组蛋白的快速分离和纯化。 此外,本发明的方法可用于生产小而通常难以表达的多肽或蛋白质,以及对宿主细胞如大肠杆菌毒性的那些蛋白质。 本发明还提供了用于本发明中用于产生多肽的质粒,载体和宿主细胞,以及使用这些载体和宿主细胞产生多肽的方法。 本发明进一步提供了用于蛋白质凝胶电泳的蛋白质分子梯度的制备方法,以及通过这些方法制备的蛋白质和蛋白质分子量梯。