Davies J, Dawkes A C, Haymes A G, Roberts C J, Sunderland R F, Wilkins M J, Davies M C, Tendler S J, Jackson D E, Edwards J C
Kodak Clinical Diagnostics Ltd. (KCDL), Pollards Wood Laboratories, Chalfont-St.-Giles, Buckinghamshire, UK.
J Immunol Methods. 1994 Jan 3;167(1-2):263-9. doi: 10.1016/0022-1759(94)90095-7.
An antiferritin antibody was either, (a) passively adsorbed to microwells or (b) biotinylated and immobilised to streptavidin coated microwells. Scanning tunnelling microscope (STM) imaging of these well surfaces coated with a platinum (95%) carbon (5%) coating (Pt/C) conductive layer showed a randomly oriented array of antibodies for passive adsorption whereas for biotin-streptavidin immobilisation there was a more uniform and even distribution of antibodies on the well surface. On further incubation with ferritin STM imaging showed that for passive adsorption approximately 5% of the surface was functional, while for the biotinylated antibody it was greater than 60%. The images presented in this paper show graphically the loss of functionality that occurs using passive adsorption and, conversely, the preservation of antibody functionality using the biotin-streptavidin linkage for antibody immobilisation. These results correlate well with the work of others in the field.
抗铁蛋白抗体要么(a)被动吸附到微孔板上,要么(b)进行生物素化并固定到包被有链霉亲和素的微孔板上。对这些涂有铂(95%)-碳(5%)涂层(Pt/C)导电层的孔表面进行扫描隧道显微镜(STM)成像显示,对于被动吸附,抗体呈现随机排列的阵列,而对于生物素-链霉亲和素固定,孔表面抗体分布更均匀、更平整。与铁蛋白进一步孵育后,STM成像显示,对于被动吸附,约5%的表面具有功能,而对于生物素化抗体,该比例大于60%。本文展示的图像直观地显示了使用被动吸附时发生的功能丧失,相反,使用生物素-链霉亲和素连接进行抗体固定时抗体功能得以保留。这些结果与该领域其他研究人员的工作结果高度相关。