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针对溶血巴斯德氏菌白细胞毒素的中和单克隆抗体可从粗培养上清液中亲和纯化该毒素。

Neutralizing monoclonal antibodies to Pasteurella haemolytica leukotoxin affinity-purify the toxin from crude culture supernatants.

作者信息

Gentry M J, Srikumaran S

机构信息

Department of Veterinary Science, University of Nebraska, Lincoln 68583-0905.

出版信息

Microb Pathog. 1991 May;10(5):411-7. doi: 10.1016/0882-4010(91)90086-p.

Abstract

The leukotoxin of Pasteurella haemolytica is a major virulence factor of the organism. It is an unstable protein which has proven very difficult to purify using traditional techniques. Hybridomas secreting monoclonal antibodies (mAbs) to P. haemolytica leukotoxin were derived from spleen cells of a mouse immunized with crude culture supernatant. Five hybridomas secreting mAbs specific for the leukotoxin were stabilized. Each of the mAbs reacted with a protein of approximately 100 kDa in toxic culture supernatants, and two of them completely neutralized the toxin in vitro. Affinity chromatography of crude culture supernatant on a column prepared with one of the neutralizing mAbs resulted in the isolation of biologically active toxin.

摘要

溶血巴氏杆菌的白细胞毒素是该生物体的主要毒力因子。它是一种不稳定的蛋白质,事实证明,使用传统技术很难将其纯化。分泌针对溶血巴氏杆菌白细胞毒素的单克隆抗体(mAb)的杂交瘤源自用粗培养上清液免疫的小鼠的脾细胞。稳定了五个分泌对白细胞毒素具有特异性的单克隆抗体的杂交瘤。每种单克隆抗体都与有毒培养上清液中一种约100 kDa的蛋白质发生反应,其中两种在体外完全中和了毒素。用其中一种中和性单克隆抗体制备的柱子对粗培养上清液进行亲和层析,从而分离出了具有生物活性的毒素。

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