Antibody Discovery and Protein Engineering, Research, MedImmune, Cambridge, United Kingdom.
PLoS One. 2013 Dec 6;8(12):e83202. doi: 10.1371/journal.pone.0083202. eCollection 2013.
Huwentoxin-IV (HwTx-IV) is a 35-residue neurotoxin peptide with potential application as a novel analgesic. It is a member of the inhibitory cystine knot (ICK) peptide family, characterised by a compact globular structure maintained by three intramolecular disulfide bonds. Here we describe a novel strategy for producing non-tagged, fully folded ICK-toxin in a bacterial system. HwTx-IV was expressed as a cleavable fusion to small ubiquitin-related modifier (SUMO) in the cytoplasm of the SHuffle T7 Express lysY Escherichia coli strain, which allows cytosolic disulfide bond formation. Purification by IMAC with selective elution of monomeric SUMO fusion followed by proteolytic cleavage and polishing chromatographic steps yielded pure homogeneous toxin. Recombinant HwTx-IV is produced with a C-terminal acid, whereas the native peptide is C-terminally amidated. HwTx-IV(acid) inhibited Nav1.7 in a dose dependent manner (IC50 = 463-727 nM). In comparison to HwTx-IV(amide) (IC50 = 11 ± 3 nM), the carboxylate was ~50 fold less potent on Nav1.7, which highlights the impact of the C-terminus. As the amide bond of an additional amino acid may mimic the carboxamide, we expressed the glycine-extended analogue HwTx-IV(G36)(acid) in the SUMO/SHuffle system. The peptide was approximately three fold more potent on Nav1.7 in comparison to HwTx-IV(acid) (IC50 = 190 nM). In conclusion, we have established a novel system for expression and purification of fully folded and active HwTx-IV(acid) in bacteria, which could be applicable to other structurally complex and cysteine rich peptides. Furthermore, we discovered that glycine extension of HwTx-IV(acid) restores some of the potency of the native carboxamide. This finding may also apply to other C-terminally amidated peptides produced recombinantly.
蜂毒素-IV(HwTx-IV)是一种由 35 个残基组成的神经毒素肽,具有作为新型镇痛药的应用潜力。它是抑制性半胱氨酸结(ICK)肽家族的成员,其特征是通过三个分子内二硫键维持紧凑的球状结构。在这里,我们描述了一种在细菌系统中生产无标签、完全折叠的 ICK-毒素的新策略。HwTx-IV 在细胞质中作为小泛素相关修饰物(SUMO)的可切割融合物在 SHuffle T7 Express lysY 大肠杆菌菌株中表达,这允许细胞内形成二硫键。通过 IMAC 进行纯化,通过选择性洗脱单体 SUMO 融合物,然后进行蛋白水解切割和抛光色谱步骤,得到纯均一的毒素。重组 HwTx-IV 带有 C 末端酸,而天然肽的 C 末端酰胺化。HwTx-IV(acid)以剂量依赖的方式抑制 Nav1.7(IC50=463-727 nM)。与 HwTx-IV(amide)(IC50=11±3 nM)相比,羧酸对 Nav1.7 的效力约低 50 倍,这突出了 C 末端的影响。由于额外氨基酸的酰胺键可能模拟羧酰胺,我们在 SUMO/SHuffle 系统中表达了甘氨酸扩展类似物 HwTx-IV(G36)(acid)。与 HwTx-IV(acid)相比,该肽对 Nav1.7 的效力约提高了三倍(IC50=190 nM)。总之,我们已经建立了一种在细菌中表达和纯化完全折叠和活性 HwTx-IV(acid)的新型系统,该系统可应用于其他结构复杂和富含半胱氨酸的肽。此外,我们发现 HwTx-IV(acid)的甘氨酸扩展恢复了天然羧酰胺的部分效力。这一发现也可能适用于其他重组产生的 C 末端酰胺化肽。