Ipsen Bioinnovation Ltd., 102 Park Drive, Milton Park, Abingdon OX14 4RY, UK.
Toxins (Basel). 2018 May 11;10(5):195. doi: 10.3390/toxins10050195.
We have purified and characterized recombinant botulinum neurotoxin serotype FA (BoNT/FA). This protein has also been named as a new serotype (serotype H), but the classification has been controversial. A lack of well-characterized, highly pure material has been a roadblock to study. Here we report purification and characterization of enzymatically active, and of inactive nontoxic, recombinant forms of BoNT/FA as tractable alternatives to purifying this neurotoxin from native . BoNT/FA cleaves the same intracellular target proteins as BoNT/F1 and other F serotype BoNTs; the intracellular targets are vesicle associated membrane proteins (VAMP) 1, 2 and 3. BoNT/FA cleaves the same site in VAMP-2 as BoNT/F5, which is different from the cleavage site of other F serotype BoNTs. BoNT/FA has slower enzyme kinetics than BoNT/F1 in a cell-free protease assay and is less potent at inhibiting ex vivo nerve-stimulated skeletal muscle contraction. In contrast, BoNT/FA is more potent at inhibiting neurotransmitter release from cultured neurons.
我们已经纯化并鉴定了重组肉毒梭菌神经毒素血清型 FA(BoNT/FA)。这种蛋白也被命名为一个新的血清型(血清型 H),但分类一直存在争议。缺乏经过充分鉴定的、高度纯化的材料是研究的一个障碍。在这里,我们报告了具有酶活性的、以及无毒性的、非活性的重组形式的 BoNT/FA 的纯化和鉴定,这是从天然 BoNT/FA 中纯化这种神经毒素的可行替代方法。BoNT/FA 切割与 BoNT/F1 和其他 F 型 BoNTs 相同的细胞内靶蛋白;细胞内靶标是囊泡相关膜蛋白(VAMP)1、2 和 3。BoNT/FA 在细胞外蛋白酶测定中,在 VAMP-2 上的切割位点与 BoNT/F5 相同,这与其他 F 型 BoNTs 的切割位点不同。与 BoNT/F1 相比,BoNT/FA 在无细胞蛋白酶测定中的酶动力学较慢,在体外神经刺激骨骼肌收缩抑制方面的效力较低。相比之下,BoNT/FA 在抑制培养神经元神经递质释放方面的效力更高。