会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 7. 发明授权
    • Methods and materials for the synthesis of modified peptides
    • 用于合成修饰肽的方法和材料
    • US07301006B2
    • 2007-11-27
    • US10622078
    • 2003-07-16
    • Travis G. YoungLaura L. Kiessling
    • Travis G. YoungLaura L. Kiessling
    • C07C247/04C07C247/06C07C247/18C07K1/06
    • C07K1/1072C07C271/22Y02P20/55
    • Methods and protected amino acids useful as building blocks (protected monomers) for the synthesis of peptides and proteins that are selectively modified at one or more side-chain hydroxyl groups. Azide-bearing protecting groups allow the selective deprotection of side-chain hydroxyl groups of amino acids after synthesis of a peptide. Reaction conditions for removal of the azide-bearing protecting group can be selected which are substantially orthogonal to those that will remove α-amino protecting groups typically employed in peptide synthesis, such that hydroxyl groups protected with the azide-bearing protecting group remain protected during synthesis of the peptide chain. Various protecting groups which are readily available can be used for protecting potentially reactive side chain groups of amino acids in the peptide or protein to be modified. Preferred side-chain protecting groups are chemically distinguishable from the azide-bearing protecting group and substantially orthogonal reaction conditions can be selected such that side-chain protection of other amino acids is maintained when the azide-bearing protecting group is removed. The use of the azide-bearing protecting group of this invention for one or more hydroxy amino acids during peptide synthesis allows the selective unmasking of those azide-protected side-chain hydroxyl groups and selective modification of the hydroxyl groups that are selectively unmasked. The methods and materials herein are particularly used in synthesis of sulfated, phosphorylated and glycosylated peptides and proteins. Kits and methods of synthesizing a modified peptide or protein using the kits are also provided.
    • 用作合成在一个或多个侧链羟基上选择性修饰的肽和蛋白质的结构单元(保护单体)的方法和保护的氨基酸。 含有叠氮基的保护基允许在合成肽后氨基酸的侧链羟基的选择性去保护。 可以选择用于除去含叠氮基保护基团的反应条件,其基本上与将除去通常用于肽合成中的α-氨基保护基团正交的那些,使得在含有叠氮基保护基团的情况下保护的羟基在合成期间保持保护 的肽链。 易于获得的各种保护基团可用于保护待修饰的肽或蛋白质中氨基酸的潜在的活性侧链基团。 优选的侧链保护基团与含叠氮基保护基团在化学上是可区分的,并且可以选择基本上正交的反应条件,使得当除去含叠氮保护基团时,维持其它氨基酸的侧链保护。 在肽合成期间使用本发明的含叠氮保护基的一个或多个羟基氨基酸允许选择性地掩蔽那些叠氮化物保护的侧链羟基并选择性地修饰选择性地未掩蔽的羟基。 本文的方法和材料特别用于硫酸化,磷酸化和糖基化肽和蛋白质的合成。 还提供了使用试剂盒合成修饰的肽或蛋白质的试剂盒和方法。