College of Life Science, State Key Laboratory of Developmental Biology of Freshwater Fish, Hunan Normal University, Changsha 410081, People's Republic of China.
J Agric Food Chem. 2020 May 27;68(21):5816-5824. doi: 10.1021/acs.jafc.0c01172. Epub 2020 May 13.
Although the new dual model of the insecticidal mechamism indicated that both Cry1A protoxin and activated toxin have the potency to kill insects, the difference in the toxic pathways elicited by the protoxin and activated toxin was less understood at the molecular level. Through utilizing the CF-203 cell line derived from the midgut of , we found that there existed obvious differences in the binding sites and endocytosis pathways for the two forms of Cry1Ac. In addition, it was revealed that Cry1Ac protoxin existed predominantly in the midgut of at the early stage after ingesting Cry1Ac crystals, which brought about obvious damage to the midgut epithelium and exhibited different binding sites on the brush border membrane vesicle compared to the toxin. These findings supported the dual mode of action of Cry1A proteins and improved our understanding of the molecular features that contribute to the protoxin toxicity.
尽管新型杀虫机制的双重模式表明 Cry1A 原毒素和激活毒素都具有杀虫活性,但在分子水平上,原毒素和激活毒素所引发的毒性途径的差异还不太清楚。通过利用源自 的中肠的 CF-203 细胞系,我们发现两种形式的 Cry1Ac 在结合部位和内化途径上存在明显差异。此外,研究还表明,在摄入 Cry1Ac 晶体后早期,Cry1Ac 原毒素主要存在于 的中肠中,这对中肠上皮造成了明显的损伤,并与毒素相比,在刷状缘膜囊泡上表现出不同的结合部位。这些发现支持了 Cry1A 蛋白的双重作用模式,并提高了我们对导致原毒素毒性的分子特征的理解。