Rudolph R, Lilie H
Institut für Biotechnolgie, Martin-Luther-Universität Halle-Wittenberg, Germany.
FASEB J. 1996 Jan;10(1):49-56.
Insoluble, inactive inclusion bodies are frequently formed upon recombinant protein production in transformed microorganisms. These inclusion bodies, which contain the recombinant protein in an highly enriched form, can be isolated by solid/liquid separation. After solubilization, native proteins can be generated from the inactive material by using in vitro folding techniques. New folding procedures have been developed for efficient in vitro reconstitution of complex hydrophobic, multidomain, oligomeric, or highly disulfide-bonded proteins. These protocols take into account process parameters such as protein concentration, catalysis of disulfide bond formation, temperature, pH, and ionic strength, as well as specific solvent ingredients that reduce unproductive side reactions. Modification of the protein sequence has been exploited to improve in vitro folding.
在转化微生物中生产重组蛋白时,经常会形成不溶性、无活性的包涵体。这些包涵体以高度富集的形式包含重组蛋白,可通过固液分离进行分离。溶解后,可通过体外折叠技术从无活性物质中生成天然蛋白。已开发出新的折叠程序,用于高效体外重构复杂的疏水、多结构域、寡聚或高度二硫键连接的蛋白。这些方案考虑了诸如蛋白质浓度、二硫键形成的催化作用、温度、pH值和离子强度等工艺参数,以及减少非生产性副反应的特定溶剂成分。已利用蛋白质序列修饰来改善体外折叠。