Ap. Quist et al., IMAGING OF SINGLE ANTIGENS, ANTIBODIES, AND SPECIFIC IMMUNOCOMPLEX FORMATION BY SCANNING FORCE MICROSCOPY, Scanning microscopy, 9(2), 1995, pp. 395-400
The most sensitive analytical techniques available today for detecting
immune assay complexes are radio or enzyme immune analytical techniqu
es, by which quantities of 10(7)-10(8) analyte molecules can be detect
ed. With the introduction of scanning force microscopy, a new method f
or detecting biological processes became available. Here, we examine t
he feasibility of using scanning force microscopy as a biosensitive to
ol. We demonstrate that single or multiple rabbit anti-human serum alb
umin molecules form complexes with preadsorbed single human serum albu
min molecules on mica. However, no interaction is observed between hum
an immunoglobulin G molecules and preadsorbed single albumin molecules
; only separate antigens and antibodies are observed at random positio
ns on the mica. This shows the ability of scanning force microscopy to
act as a biosensor for detection of immunocomplexes, and to act as a
very powerful tool to study molecule-surface interactions in general.