Knappik A, Krebber C, Plückthun A
Max-Planck-Institut für Biochemie, Protein Engineering Group, Martinsried, Fed. Rep. Germany.
Biotechnology (N Y). 1993 Jan;11(1):77-83. doi: 10.1038/nbt0193-77.
The Fv and Fab fragment and both orientations of the single-chain Fv fragment (VH-linker-VL and VL-linker-VH) of an antibody can be expressed in functional form in the periplasm of Escherichia coli, but the yield of these correctly assembled proteins is limited by the periplasmic folding process. While the periplasmic E. coli disulfide isomerase DsbA is required for this assembly, its functional over-expression does not significantly change the folding limit. Similarly, the functionally over-expressed E. coli proline cis-trans isomerase does not change the amount of all but one of the antibody fragments, not even if DsbA is over-expressed as well. Therefore, aggregation steps in the periplasm appear to compete with periplasmic folding, and they may occur before disulfide formation and/or proline cis-trans isomerization takes place and be independent of their extent.
抗体的Fv和Fab片段以及单链Fv片段的两种方向(VH-连接子-VL和VL-连接子-VH)都可以在大肠杆菌周质中以功能形式表达,但这些正确组装的蛋白质的产量受到周质折叠过程的限制。虽然周质中的大肠杆菌二硫键异构酶DsbA是这种组装所必需的,但其功能性过表达不会显著改变折叠极限。同样,功能性过表达的大肠杆菌脯氨酸顺反异构酶不会改变除一种抗体片段外的所有片段的量,即使DsbA也过表达也是如此。因此,周质中的聚集步骤似乎与周质折叠相互竞争,它们可能在二硫键形成和/或脯氨酸顺反异构化发生之前就已发生,并且与它们的程度无关。