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    • 21. 发明授权
    • Synthesis of proteins by native chemical ligation
    • 通过天然化学结合合成蛋白质
    • US06184344B2
    • 2001-02-06
    • US08945997
    • 1998-02-12
    • Stephen B. H. KentTom W. MuirPhilip E. Dawson
    • Stephen B. H. KentTom W. MuirPhilip E. Dawson
    • C07K102
    • C07K1/04C07K1/026
    • Proteins of moderate size having native peptide backbones are produced by a method of native chemical ligation. Native chemical ligation employs a chemoselective reaction of two unprotected peptide segments to produce a transient thioester-linked intermediate. The transient thioester-linked intermediate then spontaneously undergoes a rearrangement to provide the full length ligation product having a native peptide bond at the ligation site. Full length ligation products are chemically identical to proteins produced by cell free synthesis. Full length ligation products may be refolded and/or oxidized, as allowed, to form native disulfide-containing protein molecules. The technique of native chemical ligation is employable for chemically synthesizing full length proteins.
    • 通过天然化学连接的方法产生具有天然肽骨架的中等体积的蛋白质。 天然化学连接采用两个未保护肽段的化学选择性反应产生瞬时硫酯连接的中间体。 然后瞬时硫酯连接的中间体自发地进行重排,以在连接位点提供具有天然肽键的全长连接产物。 全长连接产物与通过无细胞合成产生的蛋白质化学相同。 如所允许的,全长连接产物可以重折叠和/或氧化以形成天然二硫化物的蛋白质分子。 天然化学连接的技术可用于化学合成全长蛋白质。