Selective posttranslational modification of phage-displayed polypeptides
    1.
    发明授权
    Selective posttranslational modification of phage-displayed polypeptides 有权
    噬菌体展示多肽的选择性翻译后修饰

    公开(公告)号:US08367588B2

    公开(公告)日:2013-02-05

    申请号:US11992341

    申请日:2006-10-11

    IPC分类号: C40B50/06

    摘要: The invention relates to posttranslational modification of phage-displayed polypeptides. These displayed polypeptides comprise at least one unnatural amino acid, e.g., an aryl-azide amino acid such as p-azido-L-phenylalanine, or an alkynyl-amino acid such as para-propargyloxyphenylalanine, which are incorporated into the phage-displayed fusion polypeptide at a selected position by using an in vivo orthogonal translation system comprising a suitable orthogonal aminoacyl-tRNA synthetase and a suitable orthogonal tRNA species. These unnatural amino acids advantageously provide targets for posttranslational modifications such as azide-alkyne [3+2]cycloaddition reactions and Staudinger modifications.

    摘要翻译: 本发明涉及噬菌体展示多肽的翻译后修饰。 这些显示的多肽包含至少一个非天然氨基酸,例如芳基叠氮氨基酸如对叠氮基-L-苯丙氨酸或炔基 - 氨基酸如对 - 炔丙氧基苯丙氨酸,其被并入噬菌体展示的融合物 通过使用包含合适的正交氨酰-tRNA合成酶和合适的正交tRNA物质的体内正交翻译系统,在选定位置上的多肽。 这些非天然氨基酸有利地提供翻译后修饰的靶标,例如叠氮炔 - 炔[3 + 2]环加成反应和施陶丁格修饰。

    Selective Posttranslational Modification of Phage-Displayed Polypeptides
    2.
    发明申请
    Selective Posttranslational Modification of Phage-Displayed Polypeptides 有权
    噬菌体展示多肽的选择性翻译后修饰

    公开(公告)号:US20090137424A1

    公开(公告)日:2009-05-28

    申请号:US11992341

    申请日:2006-10-11

    IPC分类号: C40B40/02 C12N7/00

    摘要: The invention relates to posttranslational modification of phage-displayed polypeptides. These displayed polypeptides comprise at least one unnatural amino acid, e.g., an aryl-azide amino acid such asp-azido-L-phenylalanine, or an alkynyl-amino acid such as para-propargyloxyphenylalanine, which are incorporated into the phage-displayed fusion polypeptide at a selected position by using an in vivo orthogonal translation system comprising a suitable orthogonal aminoacyl-tRNA synthetase and a suitable orthogonal tRNA species. These unnatural amino acids advantageously provide targets for posttranslational modifications such as azide-alkyne [3+2]cycloaddition reactions and Staudinger modifications.

    摘要翻译: 本发明涉及噬菌体展示多肽的翻译后修饰。 这些显示的多肽包含至少一个非天然氨基酸,例如芳基叠氮化物氨基酸,例如叠氮基-L-苯丙氨酸,或炔基 - 氨基酸如对 - 炔丙氧基苯丙氨酸,其被并入噬菌体展示的融合多肽 通过使用包含合适的正交氨酰-tRNA合成酶和合适的正交tRNA物质的体内正交翻译系统在选定的位置。 这些非天然氨基酸有利地提供翻译后修饰的靶标,例如叠氮炔 - 炔[3 + 2]环加成反应和施陶丁格修饰。

    Selective posttranslational modification of phage-displayed polypeptides
    3.
    发明授权
    Selective posttranslational modification of phage-displayed polypeptides 有权
    噬菌体展示多肽的选择性翻译后修饰

    公开(公告)号:US08586340B2

    公开(公告)日:2013-11-19

    申请号:US11580223

    申请日:2006-10-11

    IPC分类号: C12N7/02 C40B40/02

    摘要: The invention relates to posttranslational modification of phage-displayed polypeptides. These displayed polypeptides comprise at least one unnatural amino acid, e.g., an aryl-azide amino acid such as p-azido-L-phenylalanine, or an alkynyl-amino acid such as para-propargyloxyphenylalanine, which are incorporated into the phage-displayed fusion polypeptide at a selected position by using an in vivo orthogonal translation system comprising a suitable orthogonal aminoacyl-tRNA synthetase and a suitable orthogonal tRNA species. These unnatural amino acids advantageously provide targets for posttranslational modifications such as azide-alkyne [3+2] cycloaddition reactions and Staudinger modifications.

    摘要翻译: 本发明涉及噬菌体展示多肽的翻译后修饰。 这些显示的多肽包含至少一个非天然氨基酸,例如芳基叠氮氨基酸如对叠氮基-L-苯丙氨酸或炔基 - 氨基酸如对 - 炔丙氧基苯丙氨酸,其被并入噬菌体展示的融合物 通过使用包含合适的正交氨酰-tRNA合成酶和合适的正交tRNA物质的体内正交翻译系统,在选定位置上的多肽。 这些非天然氨基酸有利地提供翻译后修饰的靶标,例如叠氮炔 - 炔[3 + 2]环加成反应和施陶丁格修饰。

    Selective posttranslational modification of phage-displayed polypeptides
    4.
    发明申请
    Selective posttranslational modification of phage-displayed polypeptides 有权
    噬菌体展示多肽的选择性翻译后修饰

    公开(公告)号:US20070178448A1

    公开(公告)日:2007-08-02

    申请号:US11580223

    申请日:2006-10-11

    IPC分类号: C12Q1/70 C12N7/01

    摘要: The invention relates to posttranslational modification of phage-displayed polypeptides. These displayed polypeptides comprise at least one unnatural amino acid, e.g., an aryl-azide amino acid such as p-azido-L-phenylalanine, or an alkynyl-amino acid such as para-propargyloxyphenylalanine, which are incorporated into the phage-displayed fusion polypeptide at a selected position by using an in vivo orthogonal translation system comprising a suitable orthogonal aminoacyl-tRNA synthetase and a suitable orthogonal tRNA species. These unnatural amino acids advantageously provide targets for posttranslational modifications such as azide-alkyne [3+2] cycloaddition reactions and Staudinger modifications.

    摘要翻译: 本发明涉及噬菌体展示多肽的翻译后修饰。 这些显示的多肽包含至少一个非天然氨基酸,例如芳基叠氮氨基酸如对叠氮基-L-苯丙氨酸或炔基 - 氨基酸如对 - 炔丙氧基苯丙氨酸,其被并入噬菌体展示的融合物 通过使用包含合适的正交氨酰-tRNA合成酶和合适的正交tRNA物质的体内正交翻译系统,在选定位置上的多肽。 这些非天然氨基酸有利地提供翻译后修饰的靶标,例如叠氮炔 - 炔[3 + 2]环加成反应和施陶丁格修饰。

    Wing chair
    9.
    外观设计
    Wing chair 有权
    翼椅

    公开(公告)号:USD619385S1

    公开(公告)日:2010-07-13

    申请号:US29315708

    申请日:2009-07-16

    申请人: Peter Schultz

    设计人: Peter Schultz