Solid Phase PEGylation of Uricase

被引:3
|
作者
Nanda, Pooja [1 ]
Babu, P. E. Jagadeesh [1 ]
机构
[1] Natl Inst Technol Karnataka, Dept Chem Engn, Mangalore, India
关键词
Uricase; Thiol PEGylation; Solid phase; Bioactivity; Separation; PROTEIN PEGYLATION;
D O I
10.1016/j.matpr.2017.06.407
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Uricase is used as a therapeutic enzyme to treat gout and hyperuricemia which also finds application in cancer chemotherapy. Site-specific PEGylation of uricase using methoxy polyethylene glycol maleimide (mPEG-mal) through thiol PEGylation reaction is an effective way to overcome the demerit of its short plasma half-life in blood as well as for the enhancement of its therapeutic potential. However, conventional solution-phase PEGylation for the synthesis of conjugates leads to lower yields of the desired PEGylated product and thus falls short of commercial attraction. In order to preserve the bioactivity of PEGylated product, selectivity, and extent of covalent conjugation, a methodology for on-column/solid phase PEGylation of uricase enzyme using size-exclusion reaction chromatography (SERC) has been attempted. Sephadex G-100 was used as a chromatographic solid media, wherein synthesis of mono and di-PEGylated uricase molecules was observed which were efficiently separated from their non-PEGylated counterparts. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:10494 / 10497
页数:4
相关论文
共 50 条
  • [21] PEGylation of gold-decorated silica nanoparticles in the aerosol phase
    Lei, Pingyan
    Girshick, Steven L.
    NANOTECHNOLOGY, 2013, 24 (33)
  • [22] Solid-Phase N-Terminus PEGylation of Recombinant Human Fibroblast Growth Factor 2 on Heparin-Sepharose Column
    Huang, Zhifeng
    Ye, Chaohui
    Liu, Zhijun
    Wang, Xiaojie
    Chen, Huaibin
    Liu, Yanlong
    Tang, Lu
    Zhao, Hongxin
    Wang, Junfeng
    Feng, Wenke
    Li, Xiaokun
    BIOCONJUGATE CHEMISTRY, 2012, 23 (04) : 740 - 750
  • [23] MONKEY URICASE
    SIMKIN, PA
    HEALEY, LA
    SMUCKLER, E
    NEW ENGLAND JOURNAL OF MEDICINE, 1970, 283 (15): : 823 - &
  • [24] A Compartmented Microfluidic Reactor for Protein Modification Via Solid-phase Reactions — Semi-automated Examination of Two PEGylation Routes
    Regina Fraas
    Jonas Ferdinand Hübner
    Juliane Diehm
    Ramona Faas
    Rudolf Hausmann
    Matthias Franzreb
    Biotechnology and Bioprocess Engineering, 2019, 24 : 382 - 394
  • [25] Solid-phase PEGylation of recombinant interferon α-2a for site-specific modification:: Process performance, characterization, and in vitro bioactivity
    Lee, Byung Kook
    Kwon, Jin Sook
    Kim, Hyung Jin
    Yamamoto, Shuichi
    Lee, E. K.
    BIOCONJUGATE CHEMISTRY, 2007, 18 (06) : 1728 - 1734
  • [26] A Compartmented Microfluidic Reactor for Protein Modification Via Solid-phase Reactions Semi-automated Examination of Two PEGylation Routes
    Fraas, Regina
    Huebner, Jonas Ferdinand
    Diehm, Juliane
    Faas, Ramona
    Hausmann, Rudolf
    Franzreb, Matthias
    BIOTECHNOLOGY AND BIOPROCESS ENGINEERING, 2019, 24 (02) : 382 - 394
  • [27] Purification of uricase
    Holmberg, CG
    NATURE, 1939, 143 : 604 - 604
  • [28] PREPARATION OF URICASE
    LEONE, E
    BIOCHEMICAL JOURNAL, 1953, 54 (03) : 393 - 396
  • [29] The purification of uricase
    Davidson, JN
    BIOCHEMICAL JOURNAL, 1938, 32 : 1386 - 1388
  • [30] Purified uricase
    Davidson, JN
    NATURE, 1938, 141 : 790 - 790