Evidence has been obtained for the existence of lateral heterogeneity in fluid bilayers composed of mixtures of saturated and unsaturated phospholipids by use of nearest-neighbor recognition ( NNR ) methods [Vigmond, S. J.; Dewa, T.; Regen, S. L. J. Am. Chem. Soc ., 1995, 117, 7838]. Disulfide-based dimers were synthesized from a homologous series of saturated phosphoethanolamines (PEs) and analogous PEs bearing one or two double bonds and were chemically equilibrated in the bilayer state via thiolate−disulfide interchange reactions. The magnitude of NNR that was observed in these systems (i.e., the thermodynamic preference for homodimer formation) was found to correlate with the difference between the gel-to-liquid crystalline phase transition temperatures of the homodimers that were present; the larger the difference, the greater the recognition. Inclusion of 40 mol % of cholesterol had very little influence on the extent of NNR . Dilution of two membranes that showed the largest extent of recognition, with a nonexchangable phospholipid (1,2-dimyristoyl- sn -glycero-3-phosphocholine), resulted in a significant reduction in NNR . These results provide compelling evidence for the existence of lateral heterogeneity in the absence of this diluent. The implications of these findings, with respect to the two-dimensional structure of biological membranes, are briefly discussed.
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Dewa et al. (1996) studied this question.
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