A facile method for immunofluorescence microscopy of highly autofluorescent human retinal sections using nanoparticles with large Stokes shifts.

The human retina is rich in autofluorescent species, such as lipofuscin and melanin. Consequently, it is difficult to localize antigens in the human retina using immunofluorescence microscopy. To address this issue, we have developed a methodology to tag retinal antigens using quantum dot nanoparticles that absorb in the ultraviolet and emit in the infrared, thereby avoiding the visible spectrum. This protocol dramatically improves signal-to-background autofluorescence ratios of immunofluorescence images of human retinal sections, thus enhancing the specific fluorescence in microscopic studies. Of particular note is the ability to detect antigens within the brightly autofluorescent RPE cell layer. Copyright (c) 2010 Elsevier B.V. All rights reserved.