Slotte J Peter, Yasuda Tomokazu, Engberg Oskar, Al Sazzad Md Abdullah, Hautala Victor, Nyholm Thomas K M, Murata Michio
Department of Biochemistry, Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland.
Department of Biochemistry, Faculty of Science and Engineering, Åbo Akademi University, Turku, Finland; Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka, Japan.
Biophys J. 2017 Apr 25;112(8):1673-1681. doi: 10.1016/j.bpj.2017.03.016.
Using differential scanning calorimetry and lifetime analysis of trans-parinaric acid fluorescence, we have examined how cholesterol and cholesteryl phosphocholine (CholPC) affect gel-phase properties of palmitoyl ceramide (PCer) in 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) and 1,2-dioleyol-sn-glycero-3-phosphocholine (DOPC) bilayers. By H NMR, we also measured fluid-phase interactions among these lipids using deuterated analogs of POPC, PCer, and cholesterol. The PCer-rich gel phase in POPC bilayers (9:1 molar ratio of POPC to PCer) was partially and similarly dissolved (and thermostability decreased) by both cholesterol and CholPC (sterol was present equimolar to PCer, or in fourfold excess). In DOPC bilayers (4:1 DOPC/PCer molar ratio), CholPC was much more efficient in dissolving the PCer-rich gel phase when compared to cholesterol. This can be interpreted as indicating that PCer interaction with POPC was stronger than PCer interaction with DOPC. PCer-CholPC interactions were also more favored in DOPC bilayers compared to POPC bilayers. In the fluid POPC-rich phase, cholesterol increased the order of the acyl chain of d-PCer much more than did CholPC. In DOPC-rich fluid bilayers, both cholesterol and CholPC increased d-PCer acyl chain order, and the ordering induced by CholPC was more efficient in DOPC than in POPC bilayers. In fluid POPC bilayers, the ordering of 3-d1-cholesterol by PCer was weak. In summary, we found that in the gel phase, sterol effects on the PCer-rich gel phase were markedly influenced by the acyl chain composition of the fluid PC. The same was true for fluid-phase interactions involving the sterols. Our results further suggest that PCer did not display high affinity toward either of the sterols used. We conclude that the nature of unsaturated phospholipids (POPC versus DOPC) in bilayers has major effects on the properties of ceramide gel phases and on sterol-ceramide-phospholipid interactions in such complex bilayers.
我们使用差示扫描量热法和反式十八碳四烯酸荧光寿命分析,研究了胆固醇和胆固醇磷酸胆碱(CholPC)如何影响1-棕榈酰-2-油酰基-sn-甘油-3-磷酸胆碱(POPC)和1,2-二油酰基-sn-甘油-3-磷酸胆碱(DOPC)双层膜中棕榈酰神经酰胺(PCer)的凝胶相性质。通过氢核磁共振(H NMR),我们还使用POPC、PCer和胆固醇的氘代类似物测量了这些脂质之间的流体相相互作用。在POPC双层膜(POPC与PCer的摩尔比为9:1)中富含PCer的凝胶相,胆固醇和CholPC都能使其部分且类似地溶解(热稳定性降低)(甾醇与PCer等摩尔存在,或过量四倍)。在DOPC双层膜(DOPC/PCer摩尔比为4:1)中,与胆固醇相比,CholPC在溶解富含PCer的凝胶相方面效率更高。这可以解释为表明PCer与POPC的相互作用强于PCer与DOPC的相互作用。与POPC双层膜相比,PCer - CholPC相互作用在DOPC双层膜中也更受青睐。在富含POPC的流体相中,胆固醇比CholPC更能增加d - PCer酰基链的有序性。在富含DOPC的流体双层膜中,胆固醇和CholPC都增加了d - PCer酰基链的有序性,并且CholPC诱导的有序性在DOPC中比在POPC双层膜中更有效。在流体POPC双层膜中,PCer对3 - d1 - 胆固醇的有序化作用较弱。总之,我们发现,在凝胶相中,甾醇对富含PCer的凝胶相的影响明显受流体相PC酰基链组成的影响。涉及甾醇的流体相相互作用也是如此。我们的结果进一步表明,PCer对所使用的任何一种甾醇都没有显示出高亲和力。我们得出结论,双层膜中不饱和磷脂(POPC与DOPC)的性质对神经酰胺凝胶相的性质以及这种复杂双层膜中甾醇 - 神经酰胺 - 磷脂相互作用有重大影响。