Dynamics of molecules involved in antigen presentation: effects of fixation

Antigen presentation by MHC class II molecules can be enhanced by paraforma ldehyde fixation of antigen-presenting cells prior to assay. This treatment might be expected to aggregate membrane proteins and thus stabilize and st rengthen transient protein-protein interactions involved in intercellular c ooperation. 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 phospho rescence anisotropy, respectively. Probes were tetramethylrhodamine and ery throsin conjugates of MKD6 Fab fragments. Increasing concentrations of para formaldehyde 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 tim e 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 abo ut 40-50%. Taken together, these results suggest that fixation crosslinks c lass II molecules to each other or to other membrane proteins into structur es large enough (> 500,000 kDa) to diffuse translationally with perceptibly size-dependent rates. The fixation effects on both class II rotation and l ateral diffusion were half-maximal at paraformaldehyde concentrations of si milar to 0.2%, Possible relations between the biological effector functions of class II and the physical sizes of fixation-induced aggregates are disc ussed. (C) 1999 Elsevier Science Ltd. All rights reserved.