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Physics of a rapid CD4 lymphocyte count with colloidal gold
Author(s) -
Hansen P.,
Barry D.,
Restell A.,
Sylvia D.,
Magnin O.,
Dombkowski D.,
Preffer F.
Publication year - 2012
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.21139
Subject(s) - immunogold labelling , light scattering , suspension (topology) , particle (ecology) , particle size , surface charge , materials science , dynamic light scattering , colloid , particle aggregation , colloidal gold , labelling , biophysics , nanotechnology , scattering , optics , chemistry , physics , nanoparticle , biology , biochemistry , electron microscope , ecology , mathematics , homotopy , pure mathematics
Abstract The inherent surface charges and small diameters that confer colloidal stability to gold particle conjugates (immunogold) are detrimental to rapid cell surface labeling and distinct cluster definition in flow cytometric light scatter assays. Although the inherent immunogold surface charge prevents self aggregation when stored in liquid suspension, it also slows binding to cells to timeframes of hours and inhibits cell surface coverage. Although the small diameter of immunogold particles prevents settling when in liquid suspension, small particles have small light scattering cross sections and weak light scatter signals. We report a new, small particle lyophilized immunogold reagent that maintains activity after 42°C storage for a year and can be rapidly dissolved into stable liquid suspension for use in labelling cells with larger particle aggregates that have enhanced scattering cross section. Labeling requires less than 1 min at 20°C, which is ∼30 times faster than customary fluorescent antibody labeling. The labeling step involves neutralizing the surface charge of immunogold and creating specifically bound aggregates of gold on the cell surface. This process provides distinct side‐scatter cluster separation with blue laser light at 488 nm, which is further improved by using red laser light at 640 nm. Similar comparisons using LED light sources showed less improvement with red light, thereby indicating that coherent light scatter is of significance in enhancing side‐scatter cluster separation. The physical principles elucidated here for this technique are compatible with most flow cytometers; however, future studies of its clinical efficacy should be of primary interest in point‐of‐care applications where robust reagents and rapid results are important. © 2011 International Society for Advancement of Cytometry