Pinho R T, Dutra H S, Giovanni-De-Simone S, de Carvalho L C
Departamento de Imunologia, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
Acta Trop. 1991 Nov;50(1):29-38. doi: 10.1016/0001-706x(91)90070-z.
Glass wool, hydrophilic cotton wool, non-electrically charged BIO-GEL P2 and common tissue paper columns were used to purify trypomastigotes from a mixed Trypanosoma cruzi population grown in axenic culture medium. With all these columns, highly purified (up to 98%) trypomastigote preparations were obtained. Trypomastigote yields from cotton wool, BIO-GEL P2 and common tissue paper columns were not as high as from glass wool columns, from which yields varied from 69 to 80%. Purification on glass wool did not affect trypomastigote infectivity or virulence. Dead trypomastigotes could not be purified on glass wool columns. A glass-adherent amphiphilic peptide of 45 kDa, present in the cell membrane, was isolated from epimastigote but not from trypomastigote preparations.
使用玻璃棉、亲水性棉絮、不带电的BIO - GEL P2和普通纸巾柱从在无细胞培养基中培养的混合克氏锥虫群体中纯化锥鞭毛体。使用所有这些柱子,均获得了高度纯化(高达98%)的锥鞭毛体制剂。棉絮柱、BIO - GEL P2柱和普通纸巾柱的锥鞭毛体产量不如玻璃棉柱高,玻璃棉柱的产量在69%至80%之间变化。在玻璃棉上进行纯化不影响锥鞭毛体的感染性或毒力。死的锥鞭毛体不能在玻璃棉柱上纯化。从无鞭毛体中分离出一种存在于细胞膜中的45 kDa的玻璃粘附两亲性肽,但在锥鞭毛体制剂中未分离到。