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1.
公开(公告)号:US08729232B2
公开(公告)日:2014-05-20
申请号:US12921131
申请日:2009-03-20
申请人: Jason S. Rush , Carolyn Bertozzi
发明人: Jason S. Rush , Carolyn Bertozzi
CPC分类号: C12P21/02 , C07K2319/20
摘要: The invention features compositions and methods for site-specific modification of proteins by incorporation of an aldehyde tag. Enzymatic modification at a sulfatase motif of the aldehyde tag through action of a formylglycine generating enzyme (FGE) generates a formylglycine (FGly) residue. The aldehyde moiety of FGly residue can be exploited as a chemical handle for site-specific attachment of a moiety of interest to a polypeptide.
摘要翻译: 本发明的特征在于通过掺入醛标记蛋白的位点特异性修饰的组合物和方法。 通过甲酰甘氨酸生成酶(FGE)的作用,在醛标记的硫酸酯酶基序上进行酶促修饰产生甲酰甘氨酸(FGly)残基。 FGly残基的醛部分可以用作化学处理,用于将目标部分的位点特异性连接到多肽。
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2.
公开(公告)号:US20080187956A1
公开(公告)日:2008-08-07
申请号:US11857385
申请日:2007-09-18
申请人: Isaac S. Carrico , Brian L. Carlson , Peng Wu , Carolyn Bertozzi
发明人: Isaac S. Carrico , Brian L. Carlson , Peng Wu , Carolyn Bertozzi
CPC分类号: C07K16/00 , A61K38/1825 , A61K38/215 , A61K38/37 , A61K38/45 , A61K39/00 , C07K1/006 , C07K1/1072 , C07K1/13 , C07K14/00 , C07K14/35 , C07K14/565 , C07K16/46 , C07K2317/24 , C07K2317/40 , C07K2317/52 , C07K2317/622 , C12N9/13 , C12N9/96 , C12P21/00 , C12P21/005 , C12Y208/02
摘要: The invention features compositions and methods for site-specific modification of proteins by incorporation of an aldehyde tag. Enzymatic modification at a sulfatase motif of the aldehyde tag through action of a formylglycine generating enzyme (FGE) generates a formylglycine (FGly) residue. The aldehyde moiety of FGly residue can be exploited as a chemical handle for site-specific attachment of a moiety of interest to a polypeptide.
摘要翻译: 本发明的特征在于通过掺入醛标记蛋白的位点特异性修饰的组合物和方法。 通过甲酰甘氨酸生成酶(FGE)的作用,在醛标记的硫酸酯酶基序上进行酶促修饰产生甲酰甘氨酸(FGly)残基。 FGly残基的醛部分可以用作化学处理,用于将目标部分的位点特异性连接到多肽。
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公开(公告)号:US20060110782A1
公开(公告)日:2006-05-25
申请号:US11264463
申请日:2005-10-31
IPC分类号: C12Q1/34 , C08B37/00 , C07K14/705 , C07C247/10
CPC分类号: G01N33/6842 , A61K47/54 , A61K47/555 , C07C45/511 , C07C49/457 , C07C59/72 , C07C63/66 , C07C63/74 , C07C69/708 , C07C69/76 , C07C2601/18 , C07D207/416 , C07D207/452 , C07D249/16 , C07D495/04 , G01N33/531 , G01N33/58 , G01N33/6803
摘要: The present invention provides modified cycloalkyne compounds; and method of use of such compounds in modifying biomolecules. The present invention features a cycloaddition reaction that can be carried out under physiological conditions. In general, the invention involves reacting a modified cycloalkyne with an azide moiety on a target biomolecule, generating a covalently modified biomolecule. The selectivity of the reaction and its compatibility with aqueous environments provide for its application in vivo (e.g., on the cell surface or intracellularly) and in vitro (e.g., synthesis of peptides and other polymers, production of modified (e.g., labeled) amino acids).
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公开(公告)号:US20050148032A1
公开(公告)日:2005-07-07
申请号:US11039478
申请日:2005-01-19
申请人: Eliana Saxon , Carolyn Bertozzi
发明人: Eliana Saxon , Carolyn Bertozzi
IPC分类号: C07F9/50 , C07F9/6506 , C07F9/655 , C07F9/6561 , C07K1/02 , C07K1/04 , C07K1/107 , C12N5/02 , G01N33/53 , G01N33/567 , C12Q1/68 , C07F9/22 , C07C247/16
CPC分类号: C07K1/1077 , C07F9/5022 , C07F9/6506 , C07F9/65522 , C07F9/6561 , C07H7/02 , C07H13/00 , C07H15/203 , C07H15/26 , C07K1/023 , C07K1/04 , C07K1/1075
摘要: The present invention features a chemoselective ligation reaction that can be carried out under physiological conditions. In general, the invention involves condensation of a specifically engineered phosphine, which can provide for formation of an amide bond between the two reactive partners resulting in a final product comprising a phosphine moiety, or which can be engineered to comprise a cleavable linker so that a substituent of the phosphine is transferred to the azide, releasing an oxidized phosphine byproduct and producing a native amide bond in the final product. The selectivity of the reaction and its compatibility with aqueous environments provides for its application in vivo (e.g., on the cell surface or intracellularly) and in vitro (e.g., synthesis of peptides and other polymers, production of modified (e.g., labeled) amino acids).
摘要翻译: 本发明的特征在于可以在生理条件下进行的化学选择性连接反应。 通常,本发明涉及特异性改造的膦的缩合,其可以提供在两个反应性配对物之间形成酰胺键,产生包含膦部分的最终产物,或者可被工程化以包含可切割连接体,使得 将膦的取代基转移到叠氮化物中,释放氧化的膦副产物并在最终产物中产生天然酰胺键。 反应的选择性及其与水性环境的相容性在体内(例如,在细胞表面或细胞内)和体外(例如,肽和其他聚合物的合成,修饰(例如,标记的)氨基酸的产生 )。
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5.
公开(公告)号:US5783693A
公开(公告)日:1998-07-21
申请号:US518381
申请日:1995-08-23
申请人: Carolyn Bertozzi , Steven D. Rosen
发明人: Carolyn Bertozzi , Steven D. Rosen
摘要: Sulfated disaccharides characterized by the ability to inhibit the binding of selectin to its physiologically-relevant ligand are disclosed. Included are efficient and inexpensive methods for producing the sulfated disaccharides, and methods for their therapeutic use and in in vivo and in vitro assays.
摘要翻译: 公开了以抑制选择蛋白与其生理相关配体结合的能力为特征的硫酸化二糖。 包括用于生产硫酸化二糖的有效和便宜的方法,以及用于其治疗用途和体内和体外测定的方法。
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公开(公告)号:US09327036B2
公开(公告)日:2016-05-03
申请号:US13263129
申请日:2010-04-08
申请人: Shih-Chia Hsiao , Matthew B. Francis , Carolyn Bertozzi , Richard Mathies , Ravi Chandra , Erik Douglas , Amy Twite , Nicholas Toriello , Hiroaki Onoe
发明人: Shih-Chia Hsiao , Matthew B. Francis , Carolyn Bertozzi , Richard Mathies , Ravi Chandra , Erik Douglas , Amy Twite , Nicholas Toriello , Hiroaki Onoe
IPC分类号: C12N5/07 , C12N5/0789 , C07H21/00 , A61K47/48 , C12N5/00
CPC分类号: C12N5/0006 , A61K47/6901
摘要: The present invention provides conjugates of DNA and cells by linking the DNA to a native functional group on the cell surface. The cells can be without cell walls or can have cell walls. The modified cells can be linked to a substrate surface and used in assay or bioreactors.
摘要翻译: 本发明通过将DNA与细胞表面上的天然官能团连接来提供DNA和细胞的结合物。 细胞可以没有细胞壁或可以具有细胞壁。 修饰的细胞可以连接到底物表面并用于测定或生物反应器中。
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公开(公告)号:US20120142088A1
公开(公告)日:2012-06-07
申请号:US13263129
申请日:2010-04-08
申请人: Shih-Chia Hsiao , Matthew B. Francis , Carolyn Bertozzi , Richard Mathies , Ravi Chandra , Erik Douglas , Amy Twite , Nicholas Toriello , Hiroaki Onoe
发明人: Shih-Chia Hsiao , Matthew B. Francis , Carolyn Bertozzi , Richard Mathies , Ravi Chandra , Erik Douglas , Amy Twite , Nicholas Toriello , Hiroaki Onoe
IPC分类号: C12N5/07 , C07H21/00 , C12N5/0789 , C12N5/04
CPC分类号: C12N5/0006 , A61K47/6901
摘要: The present invention provides conjugates of DNA and cells by linking the DNA to a native functional group on the cell surface. The cells can be without cell walls or can have cell walls. The modified cells can be linked to a substrate surface and used in assay or bioreactors.
摘要翻译: 本发明通过将DNA与细胞表面上的天然官能团连接来提供DNA和细胞的缀合物。 细胞可以没有细胞壁或可以具有细胞壁。 修饰的细胞可以连接到底物表面并用于测定或生物反应器中。
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公开(公告)号:US20110250704A1
公开(公告)日:2011-10-13
申请号:US13163574
申请日:2011-06-17
申请人: Isaac S. Carrico , Brian L. Carlson , Peng Wu , Carolyn Bertozzi
发明人: Isaac S. Carrico , Brian L. Carlson , Peng Wu , Carolyn Bertozzi
CPC分类号: C07K16/00 , A61K38/1825 , A61K38/215 , A61K38/37 , A61K38/45 , A61K39/00 , C07K1/006 , C07K1/1072 , C07K1/13 , C07K14/00 , C07K14/35 , C07K14/565 , C07K16/46 , C07K2317/24 , C07K2317/40 , C07K2317/52 , C07K2317/622 , C12N9/13 , C12N9/96 , C12P21/00 , C12P21/005 , C12Y208/02
摘要: The invention features compositions and methods for site-specific modification of proteins by incorporation of an aldehyde tag. Enzymatic modification at a sulfatase motif of the aldehyde tag through action of a formylglycine generating enzyme (FGE) generates a formylglycine (FGly) residue. The aldehyde moiety of FGly residue can be exploited as a chemical handle for site-specific attachment of a moiety of interest to a polypeptide.
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公开(公告)号:US07122703B2
公开(公告)日:2006-10-17
申请号:US10384099
申请日:2003-03-06
申请人: Eliana Saxon , Carolyn Bertozzi
发明人: Eliana Saxon , Carolyn Bertozzi
CPC分类号: C07K1/1077 , C07F9/5022 , C07F9/6506 , C07F9/65522 , C07F9/6561 , C07H7/02 , C07H13/00 , C07H15/203 , C07H15/26 , C07K1/023 , C07K1/04 , C07K1/1075
摘要: The present invention features a chemoselective ligation reaction that can be carried out under physiological conditions. In general, the invention involves condensation of a specifically engineered phosphine, which can provide for formation of an amide bond between the two reactive partners resulting in a final product comprising a phosphine moiety, or which can be engineered to comprise a cleavable linker so that a substituent of the phosphine is transferred to the azide, releasing an oxidized phosphine byproduct and producing a native amide bond in the final product. The selectivity of the reaction and its compatibility with aqueous environments provides for its application in vivo (e.g., on the cell surface or intracellularly) and in vitro (e.g., synthesis of peptides and other polymers, production of modified (e.g., labeled) amino acids).
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公开(公告)号:US06552103B1
公开(公告)日:2003-04-22
申请号:US09574938
申请日:2000-05-19
IPC分类号: G02C704
CPC分类号: G02B1/043 , A61L27/16 , A61L27/52 , A61L2430/16 , C08F220/38 , C08F220/54 , Y10S524/916 , C08L51/02 , C08L33/14
摘要: Novel biomimetic hydrogel materials and methods for their preparation. Hydrogels containing acrylamide-functionalized carbohydrate, sulfoxide, sulfide or sulfone copolymerized with a hydrophilic or hydrophobic copolymerizing material selected from the group consisting of an acrylamide, methacrylamide, acrylate, methacrylate, vinyl and a derivative thereof present in concentration from about 1 to about 99 wt %. and methods for their preparation. The method of use of the new hydrogels for fabrication of soft contact lenses and biomedical implants.
摘要翻译: 新型仿生水凝胶材料及其制备方法。 含有丙烯酰胺官能化碳水化合物,亚砜,硫化物或砜的水凝胶与选自丙烯酰胺,甲基丙烯酰胺,丙烯酸酯,甲基丙烯酸酯,乙烯基及其衍生物的亲水或疏水共聚材料共聚合,其浓度为约1至约99重量% %。 及其制备方法。 使用新型水凝胶制造软性隐形眼镜和生物医学植入物的方法。
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