Post-production protein stability: trouble beyond the cell factory

被引:37
作者
Vazquez, Esther [1 ,2 ,3 ]
Luis Corchero, Jose [1 ,2 ,3 ]
Villaverde, Antonio [1 ,2 ,3 ]
机构
[1] Univ Autonoma Barcelona, Inst Biotechnol & Biomed, E-08193 Barcelona, Spain
[2] Univ Autonoma Barcelona, Dept Genet & Microbiol, E-08193 Barcelona, Spain
[3] CIBER BBN, Barcelona 08193, Spain
关键词
BACTERIAL INCLUSION-BODIES; NONVIRAL GENE-THERAPY; BLOOD-BRAIN-BARRIER; ESCHERICHIA-COLI; RECOMBINANT PROTEINS; FUSION PROTEIN; BODY FORMATION; CONFORMATIONAL QUALITY; IMPROVED SOLUBILITY; SOLUBLE EXPRESSION;
D O I
10.1186/1475-2859-10-60
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Being protein function a conformation-dependent issue, avoiding aggregation during production is a major challenge in biotechnological processes, what is often successfully addressed by convenient upstream, midstream or downstream approaches. Even when obtained in soluble forms, proteins tend to aggregate, especially if stored and manipulated at high concentrations, as is the case of protein drugs for human therapy. Post-production protein aggregation is then a major concern in the pharmaceutical industry, as protein stability, pharmacokinetics, bioavailability, immunogenicity and side effects are largely dependent on the extent of aggregates formation. Apart from acting at the formulation level, the recombinant nature of protein drugs allows intervening at upstream stages through protein engineering, to produce analogue protein versions with higher stability and enhanced therapeutic values.
引用
收藏
页数:6
相关论文
共 115 条
[81]   NATIVE-LIKE SECONDARY STRUCTURE IN INTERLEUKIN-1-BETA INCLUSION-BODIES BY ATTENUATED TOTAL REFLECTANCE FTIR [J].
OBERG, K ;
CHRUNYK, BA ;
WETZEL, R ;
FINK, AL .
BIOCHEMISTRY, 1994, 33 (09) :2628-2634
[82]   BINDING OF I-125-LABELED RECOMBINANT BETA-INTERFERON (IFN-BETA SER17) TO HUMAN-CELLS [J].
OROURKE, EC ;
DRUMMOND, RJ ;
CREASEY, AA .
MOLECULAR AND CELLULAR BIOLOGY, 1984, 4 (12) :2745-2749
[83]   Blood-brain barrier delivery of protein and non-viral gene therapeutics with molecular Trojan horses [J].
Pardridge, William M. .
JOURNAL OF CONTROLLED RELEASE, 2007, 122 (03) :345-348
[84]   Influence of production process design on inclusion bodies protein: the case of an Antarctic flavohemoglobin [J].
Parrilli, Ermenegilda ;
Giuliani, Maria ;
Marino, Gennaro ;
Tutino, Maria Luisa .
MICROBIAL CELL FACTORIES, 2010, 9
[85]  
Parveen S, 2011, NANOMEDICINE
[86]   Isolation of biologically active nanomaterial (inclusion bodies) from bacterial cells [J].
Peternel, Spela ;
Komel, Radovan .
MICROBIAL CELL FACTORIES, 2010, 9
[87]   Engineering inclusion bodies for non denaturing extraction of functional proteins [J].
Peternel, Spela ;
Grdadolnik, Joze ;
Gaberc-Porekar, Vladka ;
Komel, Radovan .
MICROBIAL CELL FACTORIES, 2008, 7 (1)
[88]   Current perspectives on stability of protein drug products during formulation, fill and finish operations [J].
Rathore, Nitin ;
Rajan, Rahul S. .
BIOTECHNOLOGY PROGRESS, 2008, 24 (03) :504-514
[89]  
Richard J, 2010, IDRUGS, V13, P550
[90]   CYSTEINE TO SERINE SUBSTITUTIONS IN BASIC FIBROBLAST GROWTH-FACTOR - EFFECT ON INCLUSION BODY FORMATION AND PROTEOLYTIC SUSCEPTIBILITY DURING INVITRO REFOLDING [J].
RINAS, U ;
TSAI, LB ;
LYONS, D ;
FOX, GM ;
STEARNS, G ;
FIESCHKO, J ;
FENTON, D ;
BAILEY, JE .
BIO-TECHNOLOGY, 1992, 10 (04) :435-440