Choi Anthony H-C, Basu Mitali, McNeal Monica M, Bean Judy A, Clements John D, Ward Richard L
Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USA.
Protein Expr Purif. 2004 Dec;38(2):205-16. doi: 10.1016/j.pep.2004.08.009.
We are developing rotavirus vaccines based on the VP6 protein of the human G1P[8] [corrected] [J. Virol. 73 (1999) 7574] CJN strain of rotavirus. One prototype candidate consisting of MBP::VP6::His6, a chimeric protein of maltose-binding protein, VP6 and hexahistidine, was expressed mainly as truncated polypeptides in Escherichia coli BL21(DE3) cells. A possible reason for this extensive truncation is the high frequencies of rare bacterial codons within the rotavirus VP6 gene. Expression of truncated recombinant VP6 was found to be reduced, and expression of complete VP6 protein was simultaneously increased, when the protein was expressed in Rosetta(DE3)pLacI E. coli cells that contain increased amounts of transfer RNAs for a selection of rare codons. The same observation was made when a synthetic codon-optimized CJN-VP6 gene was expressed in E. coli BL21 or Rosetta cells. To increase protein recovery, recombinant E. coli cells were treated with 8M urea. Denatured, full-length MBP::VP6::His6 protein was then purified and used for intranasal vaccination of BALB/c mice (2 doses administered with E. coli heat-labile toxin LT(R192G) as adjuvant). Following oral challenge with the G3P[16] [corrected] [J. Virol. 76 (2002) 560] EDIM strain of murine rotavirus, protection levels against fecal rotavirus shedding were comparable (P>0.05) between groups of mice immunized with denatured codon-optimized or native (not codon-optimized) immunogen with values ranging from 87 to 99%. These protection levels were also comparable to those found after immunization with non-denatured CJN VP6. Thus, expression of complete rotavirus VP6 protein was greatly enhanced by codon optimization, and the protection elicited was not affected by denaturation of recombinant VP6.
我们正在研发基于人G1P[8] [已校正] [《病毒学杂志》73 (1999) 7574]轮状病毒CJN株VP6蛋白的轮状病毒疫苗。一种由麦芽糖结合蛋白、VP6和六聚组氨酸组成的嵌合蛋白MBP::VP6::His6的原型候选疫苗,在大肠杆菌BL21(DE3)细胞中主要表达为截短的多肽。这种广泛截短的一个可能原因是轮状病毒VP6基因内稀有细菌密码子的高频率出现。当该蛋白在含有增加量用于选择稀有密码子的转运RNA的Rosetta(DE3)pLacI大肠杆菌细胞中表达时,发现截短的重组VP6的表达减少,而完整VP6蛋白的表达同时增加。当在大肠杆菌BL21或Rosetta细胞中表达合成的密码子优化的CJN-VP6基因时,也得到了相同的观察结果。为了提高蛋白回收率,用8M尿素处理重组大肠杆菌细胞。然后纯化变性的全长MBP::VP6::His6蛋白,并用于对BALB/c小鼠进行鼻内接种(2剂,以大肠杆菌不耐热毒素LT(R192G)作为佐剂)。在用鼠轮状病毒G3P[16] [已校正] [《病毒学杂志》76 (2002) 560] EDIM株进行口服攻击后,用变性的密码子优化或天然(未密码子优化)免疫原免疫的小鼠组之间,针对粪便轮状病毒排出的保护水平相当(P>0.05),保护率范围为87%至99%。这些保护水平也与用未变性的CJN VP6免疫后发现的保护水平相当。因此,通过密码子优化大大增强了完整轮状病毒VP6蛋白的表达,并且重组VP6的变性不影响所引发的保护作用。