Roberts C J, Davies M C, Tendler S J, Williams P M, Davies J, Dawkes A C, Yearwood G D, Edwards J C
Department of Pharmaceutical Sciences, University of Nottingham, UK.
Ultramicroscopy. 1996 Feb;62(3):149-55. doi: 10.1016/0304-3991(95)00143-3.
We have previously employed scanning force microscopy (SFM) to study antibody-antigen molecular interactions on microtiter wells used for enzyme linked immunosorbant assays (ELISA). Here we demonstrate the ability of SFM to image and discriminate different types of antibody and antibody fragments bound to an ELISA well surface. The samples studied include a type IgG antibody with a proportion of bound IgM and two-dimensional films of whole IgG antibody, and Fab' and F(ab)2 antibody fragments. Molecular resolution is achieved in each case despite the size of substrate features exceeding most of the molecular dimensions observed. Analysis of the data shows that the SFM overestimates molecular dimensions by an approximately constant amount, which is proposed to principally result from the effects of a finite probe size and not from deformation of the molecular species due to the imaging forces employed.
我们之前已采用扫描力显微镜(SFM)来研究用于酶联免疫吸附测定(ELISA)的微量滴定板上的抗体 - 抗原分子相互作用。在此,我们展示了SFM对结合在ELISA孔表面的不同类型抗体及抗体片段进行成像和鉴别的能力。所研究的样品包括含有一定比例结合IgM的IgG型抗体、完整IgG抗体的二维膜,以及Fab'和F(ab)2抗体片段。尽管底物特征的尺寸超过了所观察到的大多数分子尺寸,但在每种情况下均实现了分子分辨率。数据分析表明,SFM对分子尺寸的高估量大致恒定,这主要是由有限的探针尺寸效应导致的,而非由于所采用的成像力使分子种类发生变形所致。