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Class-ii molecules; T cells; Rotational diffusion; Mast cells; Mhc; Phosphorescence; Recognition; Anisotropy; Receptors; Surface
Abstract:
Antigen presentation by MHC class II molecules can be enhanced by paraformaldehyde fixation of antigen-presenting cells prior to assay. This treatment might be expected to aggregate membrane proteins and thus stabilize and strengthen transient protein-protein interactions involved in intercellular cooperation. Lateral and rotational dynamics of the MHC class II antigen I-A(d) on A20 cells fixed with various concentrations of paraformaldehyde were examined by fluorescence photobleaching recovery and time-resolved phosphorescence anisotropy, respectively. Probes were tetramethylrhodamine and erythrosin conjugates of MKD6 Fab fragments. Increasing concentrations of paraformaldehyde led to a progressive increase in the limiting anisotropy of I-A(d) at 4 degrees C from the value of 0.042 for untreated cells, indicative of large aggregate formation, while leaving the rotational correlation time of 29 mu s unchanged, a measure of the unperturbed molecule. On the other hand, the translational diffusion constants decreased from similar to 2 x 10(-10) cm(2) s(-1), while me fractional recovery remained unchanged at about 40-50%. Taken together, these results suggest that fixation crosslinks class II molecules to each other or to other membrane proteins into structures large enough (> 500,000 kDa) to diffuse translationally with perceptibly size-dependent rates. The fixation effects on both class II rotation and lateral diffusion were half-maximal at paraformaldehyde concentrations of similar to 0.2%, Possible relations between the biological effector functions of class II and the physical sizes of fixation-induced aggregates are discussed. (C) 1999 Elsevier Science Ltd. All rights reserved.
