A comparison of statistical approaches used for the optimization of soluble protein expression in Escherichia coli

被引:15
作者
Papaneophytou, Christos [1 ,2 ]
Kontopidis, George [1 ,2 ]
机构
[1] Univ Thessaly, Sch Vet, Trikalon 224, Kardhitsa 43100, Greece
[2] Ctr Res & Technol Hellas CERTH, Inst Res & Technol Thessaly IRETETH, Dimitriados 95 & Paulou Mela, Volos 38333, Greece
关键词
Response surface methodology; Fractional factorial approach; Design of experiments; Recombinant protein; Soluble protein expression; RESPONSE-SURFACE METHODOLOGY; RECOMBINANT PROTEINS; CRYSTALLIZATION; OVEREXPRESSION; PURIFICATION; STRATEGIES; ARTHRITIS; CULTURE; TNF;
D O I
10.1016/j.pep.2015.12.014
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
During a discovery project of potential inhibitors for three proteins, TNF-alpha, RANKL and HO-1, implicated in the pathogenesis of rheumatoid arthritis, significant amounts of purified proteins were required. The application of statistically designed experiments for screening and optimization of induction conditions allows rapid identification of the important factors and interactions between them. We have previously used response surface methodology (RSM) for the optimization of soluble expression of TNF-alpha and RANKL. In this work, we initially applied RSM for the optimization of recombinant HO-1 and a 91% increase of protein production was achieved. Subsequently, we slightly modified a published incomplete factorial approach (called IF1) in order to evaluate the effect of three expression variables (bacterial strains, induction temperatures and culture media) on soluble expression levels of the three tested proteins. However, soluble expression yields of TNF-alpha and RANKL obtained by the IF1 method were significantly lower (<50%) than those obtained by RSM. We further modified the IF1 approach by replacing the culture media with induction times and the resulted method called IF-STT (Incomplete Factorial-Stain/Temperature/Time) was validated using the three proteins. Interestingly, soluble expression levels of the three proteins obtained by IF-SIT were only 1.2-fold lower than those obtained by RSM. Although RSM is probably the best approach for optimization of biological processes, the IF-STT is faster, it examines the most important factors (bacterial strain, temperature and time) influencing protein soluble expression in a single experiment, and can be used in any recombinant protein expression project as a starting point. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:126 / 137
页数:12
相关论文
共 36 条
  • [1] Abergel Chantal, 2003, Journal of Structural and Functional Genomics, V4, P141, DOI 10.1023/A:1026177202925
  • [2] [Anonymous], 2004, DESIGN ANAL EXPT
  • [3] Blockade of interleukin 6 trans signaling suppresses T-cell resistance against apoptosis in chronic intestinal inflammation:: Evidence in Crohn disease and experimental colitis in vivo
    Atreya, R
    Mudter, J
    Finotto, S
    Müllberg, J
    Jostock, T
    Wirtz, S
    Schütz, M
    Bartsch, B
    Holtmann, M
    Becker, C
    Strand, D
    Czaja, J
    Schlaak, JF
    Lehr, HA
    Autschbach, F
    Schürmann, G
    Nishimoto, N
    Yoshizaki, K
    Ito, H
    Kishimoto, T
    Galle, PR
    Rose-John, S
    Neurath, MF
    [J]. NATURE MEDICINE, 2000, 6 (05) : 583 - 588
  • [4] Optimization of an extracellular zinc-metalloprotease (SVP2) expression in Escherichia coli BL21 (DE3) using response surface methodology
    Beigi, Laleh
    Karbalaei-Heidari, Hamid Reza
    Kharrati-Kopaei, Mahmood
    [J]. PROTEIN EXPRESSION AND PURIFICATION, 2012, 84 (01) : 161 - 166
  • [5] Expression in Escherichia coli, refolding and crystallization of Aspergillus niger feruloyl esterase A using a serial factorial approach
    Benoit, Isabelle
    Coutard, Bruno
    Oubelaid, Rachid
    Asther, Marcel
    Bignon, Christophe
    [J]. PROTEIN EXPRESSION AND PURIFICATION, 2007, 55 (01) : 166 - 174
  • [6] Recombinant protein expression and solubility screening in Escherichia coli:: a comparative study
    Berrow, Nick S.
    Buessow, K.
    Coutard, B.
    Diprose, J.
    Ekberg, M.
    Folkers, G. E.
    Levy, N.
    Lieu, V.
    Owens, R. J.
    Peleg, Y.
    Pinaglia, C.
    Quevillon-Cheruel, S.
    Salim, L.
    Scheich, C.
    Vincentelli, R.
    Busso, Didier
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2006, 62 : 1218 - 1226
  • [7] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [8] Mononuclear phagocytes and rheumatoid synovitis - Mastermind or workhorse in arthritis?
    Burmester, GR
    Stuhlmuller, B
    Keyszer, G
    Kinne, RW
    [J]. ARTHRITIS AND RHEUMATISM, 1997, 40 (01): : 5 - 18
  • [9] BURNETTE WN, 1981, ANAL BIOCHEM, V112, P195, DOI 10.1016/0003-2697(81)90281-5
  • [10] Chambers Stephen P., 2009, V498, P19, DOI 10.1007/978-1-59745-196-3_2