Engineering batch and pulse refolding with transition of aggregation kinetics: An investigation using green fluorescent protein (GFP)

被引:6
|
作者
Pan, Siqi [2 ]
Odabas, Nora [2 ]
Sissolak, Bernhard [1 ]
Imendoerffer, Moritz [2 ]
Zelger, Monika [2 ]
Jungbauer, Alois [1 ,2 ]
Hahn, Rainer [1 ,2 ]
机构
[1] Univ Nat Resources & Life Sci Vienna, Dept Biotechnol, A-1190 Vienna, Austria
[2] Austrian Ctr Ind Biotechnol, A-1190 Vienna, Austria
关键词
Inclusion bodies; Renaturation; Folding; Reaction order; GFP; SCREENING METHOD; LYSOZYME; BIOPHARMACEUTICALS; RENATURATION; COMPETITION; TECHNOLOGY; INSULIN;
D O I
10.1016/j.ces.2015.03.054
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Pulse refolding is a strategy to overcome concentration dependent aggregation, assuming that aggregation is significantly suppressed under diluted conditions. When a typical 2nd or higher order aggregation kinetics is assumed, kinetics over predicted yields at low refolding concentrations. Using GFP as our model protein, we found a transition in aggregation kinetics from 2nd to 1st order when intermediates deplete from 100 to 60 mu g/ml. Taking this transition into account, the model can better predict refolding yields in batch and pulse refolding strategies. This model is suited for the design of refolding processes since this deviation from 2nd or higher order aggregation was also previously observed in other proteins. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:91 / 100
页数:10
相关论文
共 50 条
  • [1] Refolding Circulary Permutated GFP From Inclusion Bodies; Accessing the Chromophore of Green Fluorescent Protein
    Kim, TaeSoo
    Melief, Edward
    Tonge, Peter J.
    FASEB JOURNAL, 2008, 22
  • [2] Engineering color variants of green fluorescent protein (GFP) for thermostability, pH-sensitivity, and improved folding kinetics
    Aliye, Naser
    Fabbretti, Attilio
    Lupidi, Giulio
    Tsekoa, Tsepo
    Spurio, Roberto
    APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2015, 99 (03) : 1205 - 1216
  • [3] Engineering color variants of green fluorescent protein (GFP) for thermostability, pH-sensitivity, and improved folding kinetics
    Naser Aliye
    Attilio Fabbretti
    Giulio Lupidi
    Tsepo Tsekoa
    Roberto Spurio
    Applied Microbiology and Biotechnology, 2015, 99 : 1205 - 1216
  • [4] Understanding GFP chromophore formation: Refolding circularly permutated green fluorescent protein from inclusion bodies
    Kim, TaeSoo
    FASEB JOURNAL, 2007, 21 (06): : A1006 - A1006
  • [5] Selection of transgenic Petunia plants using the green fluorescent protein (GFP)
    Mussmann, Viola
    Serek, Margrethe
    Winkelmann, Traud
    PLANT CELL TISSUE AND ORGAN CULTURE, 2011, 107 (03) : 483 - 492
  • [6] Design of a sensing system for camp using the green fluorescent protein (GFP).
    Feltus, A
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 219 : U89 - U89
  • [7] Selection of transgenic Petunia plants using the green fluorescent protein (GFP)
    Viola Mußmann
    Margrethe Serek
    Traud Winkelmann
    Plant Cell, Tissue and Organ Culture (PCTOC), 2011, 107 : 483 - 492
  • [8] Monitoring the pH of secretory vesicles using targeted green fluorescent protein (GFP).
    Tompkins, LS
    Murphy, S
    Parnami, G
    Lynch, RM
    FASEB JOURNAL, 1999, 13 (04): : A75 - A75
  • [9] Transient transfection of Cryptosporidium parvum using green fluorescent protein (GFP) as a marker
    Li, Wei
    Zhang, Nan
    Liang, Xiaoying
    Li, Jianhua
    Gong, Pengtao
    Yu, Xinyou
    Ma, Guangpeng
    Ryan, U. M.
    Zhang, Xichen
    MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2009, 168 (02) : 143 - 148
  • [10] Transfection of Leishmania tropica with Green Fluorescent Protein (gfp) Gene and Investigation of the In Vitro Drug Effect
    Ertabaklar, Hatice
    Caliskan, Sercin Ozlem
    Kolli, Bala
    Ertug, Serna
    Ozbilgin, Ahmet
    Malatyali, Erdogan
    Chang, Kwang Poo
    MIKROBIYOLOJI BULTENI, 2019, 53 (02): : 213 - 223