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    • 4. 发明授权
    • High pressure refolding of protein aggregates and inclusion bodies
    • 蛋白质聚集体和包涵体的高压重折叠
    • US06489450B2
    • 2002-12-03
    • US09350327
    • 1999-07-09
    • Theodore W. RandolphJohn F. CarpenterRichard St. John
    • Theodore W. RandolphJohn F. CarpenterRichard St. John
    • A23J100
    • C07K14/61C07K1/1133C07K1/1136C12N9/2462
    • The present disclosure provides an effective method for the refolding of denatured proteins in solution so that properly folded, biologically active protein in solution is recovered in high yield. The refolding takes place at pressures between about 0.25 kbar to about 3.5 kbar, advantageously at about 1.5 kbar to about 3 kbar. Typically a chaotropic agent is present at a concentration which is not effective for denaturing protein at atmospheric pressure, and optionally, oxidation-reduction reagents can be incorporated in the refolding solution so that native intramolecular disulfide bonds can be formed where that is desired. The method is applicable to substantially all proteins, especially after solubilization and/or denaturation of insoluble protein aggregates, inclusion bodies, or abnormal oligomeric (soluble) aggregates.
    • 本公开提供了在溶液中重折叠变性蛋白质的有效方法,从而以高产率回收溶液中适当折叠的生物活性蛋白质。 重折叠在约0.25kbar至约3.5kbar之间,有利地为约1.5kbar至约3kbar的压力下进行。 通常,离液剂以对大气压下变性蛋白质无效的浓度存在,并且任选地,氧化还原试剂可以并入再折叠溶液中,使得可以在需要的地方形成天然的分子内二硫键。 该方法适用于基本上所有蛋白质,特别是在溶解和/或变性不溶性蛋白质聚集体,包涵体或异常低聚(可溶))聚集体之后。
    • 5. 发明授权
    • High pressure refolding of protein aggregates and inclusion bodies
    • 蛋白质聚集体和包涵体的高压重折叠
    • US08710197B2
    • 2014-04-29
    • US12940587
    • 2010-11-05
    • Theodore W. RandolphJohn F. CarpenterRichard St. John
    • Theodore W. RandolphJohn F. CarpenterRichard St. John
    • C07K14/00C12N9/00
    • C07K14/61C07K1/1133C07K1/1136C12N9/2462
    • The present disclosure provides an effective method for the refolding of denatured proteins in solution so that properly folded, biologically active protein in solution is recovered in high yield. The refolding takes place at pressures between about 0.25 kbar to about 3.5 kbar, advantageously at about 1.5 kbar to about 3 kbar. Typically a chaotropic agent is present at a concentration which is not effective for denaturing protein at atmospheric pressure, and optionally, oxidation-reduction reagents can be incorporated in the refolding solution so that native intramolecular disulfide bonds can be formed where that is desired. The method is applicable to substantially all proteins, especially after solubilization and/or denaturation of insoluble protein aggregates, inclusion bodies, or abnormal oligomeric (soluble) aggregates.
    • 本公开提供了在溶液中重折叠变性蛋白质的有效方法,从而以高产率回收溶液中适当折叠的生物活性蛋白质。 重折叠在约0.25kbar至约3.5kbar之间,有利地为约1.5kbar至约3kbar的压力下进行。 通常,离液剂以对大气压下变性蛋白质无效的浓度存在,并且任选地,氧化还原试剂可以并入再折叠溶液中,使得可以在需要的地方形成天然的分子内二硫键。 该方法适用于基本上所有蛋白质,特别是在溶解和/或变性不溶性蛋白质聚集体,包涵体或异常低聚(可溶))聚集体之后。
    • 6. 发明申请
    • HIGH PRESSURE REFOLDING OF PROTEIN AGGREGATES AND INCLUSION BODIES
    • 蛋白质聚集体和包涵体的高压重塑
    • US20110046357A1
    • 2011-02-24
    • US12940587
    • 2010-11-05
    • Theodore W. RandolphJohn F. CarpenterRichard St. John
    • Theodore W. RandolphJohn F. CarpenterRichard St. John
    • C07K1/14
    • C07K14/61C07K1/1133C07K1/1136C12N9/2462
    • The present disclosure provides an effective method for the refolding of denatured proteins in solution so that properly folded, biologically active protein in solution is recovered in high yield. The refolding takes place at pressures between about 0.25 kbar to about 3.5 kbar, advantageously at about 1.5 kbar to about 3 kbar. Typically a chaotropic agent is present at a concentration which is not effective for denaturing protein at atmospheric pressure, and optionally, oxidation-reduction reagents can be incorporated in the refolding solution so that native intramolecular disulfide bonds can be formed where that is desired. The method is applicable to substantially all proteins, especially after solubilization and/or denaturation of insoluble protein aggregates, inclusion bodies, or abnormal oligomeric (soluble) aggregates.
    • 本公开提供了在溶液中重折叠变性蛋白质的有效方法,从而以高产率回收溶液中适当折叠的生物活性蛋白质。 重折叠在约0.25kbar至约3.5kbar之间,有利地为约1.5kbar至约3kbar的压力下进行。 通常,离液剂以对大气压下变性蛋白质无效的浓度存在,并且任选地,氧化还原试剂可以并入再折叠溶液中,使得可以在需要的地方形成天然的分子内二硫键。 该方法适用于基本上所有蛋白质,特别是在溶解和/或变性不溶性蛋白质聚集体,包涵体或异常低聚(可溶))聚集体之后。
    • 9. 发明授权
    • High pressure refolding of protein aggregates and inclusion bodies
    • 蛋白质聚集体和包涵体的高压重折叠
    • US07767795B2
    • 2010-08-03
    • US11341013
    • 2006-01-27
    • Theodore W. RandolphJohn F. CarpenterRichard St. John
    • Theodore W. RandolphJohn F. CarpenterRichard St. John
    • C07K14/00C12N9/00
    • C07K14/61C07K1/1133C07K1/1136C12N9/2462
    • The present disclosure provides an effective method for the refolding of denatured proteins in solution so that properly folded, biologically active protein in solution is recovered in high yield. The refolding takes place at pressures between about 0.25 kbar to about 3.5 kbar, advantageously at about 1.5 kbar to about 3 kbar. Typically a chaotropic agent is present at a concentration which is not effective for denaturing protein at atmospheric pressure, and optionally, oxidation-reduction reagents can be incorporated in the refolding solution so that native intramolecular disulfide bonds can be formed where that is desired. The method is applicable to substantially all proteins, especially after solubilization and/or denaturation of insoluble protein aggregates, inclusion bodies, or abnormal oligomeric (soluble) aggregates.
    • 本公开提供了在溶液中重折叠变性蛋白质的有效方法,从而以高产率回收溶液中适当折叠的生物活性蛋白质。 重折叠在约0.25kbar至约3.5kbar之间,有利地为约1.5kbar至约3kbar的压力下进行。 通常,离液剂以对大气压下变性蛋白质无效的浓度存在,并且任选地,氧化还原试剂可以并入再折叠溶液中,使得可以在需要的地方形成天然的分子内二硫键。 该方法适用于基本上所有蛋白质,特别是在溶解和/或变性不溶性蛋白质聚集体,包涵体或异常低聚(可溶))聚集体之后。