InXy and SeXy, compact heterologous reporter proteins for mammalian cells

被引:3
作者
Fluri, David A.
Kelm, Jens M.
Lesage, Guillaume
Baba, Marie Daoud-El
Fussenegger, Martin
机构
[1] ETH, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[2] Univ Zurich Hosp, Cardiovasc Surg Clin, CH-8091 Zurich, Switzerland
[3] Univ Zurich Hosp, Dept Surg Res, CH-8091 Zurich, Switzerland
[4] Inst Univ Technol IUTA, Dept Gen Biol, Villeurbanne, France
关键词
AAV; Bacillus subtilis; gene expression; glycosylation; mammalian reporter gene; protein secretion; protein production; SAMY; SEAP;
D O I
10.1002/bit.21461
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
Mammalian reporter proteins are essential for gene-function analysis, drugscreening initiatives and as model product proteins for biopharmaceutical manufacturing. Bacillus subtilis can maintain its metabolism by secreting Xylanase A (XynA), which converts xylan into shorter xylose oligosaccharides. XynA is a family I l xylanase monospecific for D-xylose containing substrates. Mammalian cells transgenic for constitutive expression of wild-type xynA showed substantial secretion of this prokaryotic enzyme. Deletion analysis confirmed that a prokaryotic signal sequence encoded within the first 81 nucleotides was compatible with the !, secretory pathway of mammalian cells. Codon optimization combined with elimination of the prokaryotic signal sequence resulted in an exclusively intracellular mammalian Xylanase A variant (InXy) while replacement by an immunoglobulin-derived secretion signal created an optimal secreted Xylanase A derivative (SeXy). A variety of chromogenic and fluorescence-based assays adapted for use with mammalian cells detected InXy and SeXy with high sensitivity and showed that both reporter proteins resisted repeated freeze/thaw cycles, remained active over wide temperature and pH ranges, were extremely stable in human serum stored at room temperature and could independently be quantified in samples also containing other prominent reporter proteins such as the human placental alkaline phosphatase. (SEAP) and the Bacillus stearothermophilus derived secreted alpha-amylase (SAMY). Glycoprofiling revealed that SeXy produced to mammalian cells was N-glycosylated at four different sites, mutation of which resulted in impaired secretion. SeXy was successfully expressed in a variety of mammalian cell lines and primary cells following transient transfection and transduction with adeno-associated virus particles (AAV) engineered for constitutive SeXy expression. Intramuscular injection of transgenic AAVs into mice showed significant SeXy levels in the bloodstream. InXy and SeXy are highly sensitive, compact and robust reporter proteins, fully compatible with preexisting-marker genes and can be assayed in high-throughput formats using very small sample volumes.
引用
收藏
页码:655 / 667
页数:13
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