Petruzielo Robin S, Heberle Frederick A, Drazba Paul, Katsaras John, Feigenson Gerald W
Department of Physics, Cornell University, Ithaca, NY 14853, USA.
Biochim Biophys Acta. 2013 Apr;1828(4):1302-13. doi: 10.1016/j.bbamem.2013.01.007. Epub 2013 Jan 18.
Membrane raft size measurements are crucial to understanding the stability and functionality of rafts in cells. The challenge of accurately measuring raft size is evidenced by the disparate reports of domain sizes, which range from nanometers to microns for the ternary model membrane system sphingomyelin (SM)/1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC)/cholesterol (Chol). Using Förster resonance energy transfer (FRET) and differential scanning calorimetry (DSC), we established phase diagrams for porcine brain SM (bSM)/dioleoyl-sn-glycero-3-phosphocholine (DOPC)/Chol and bSM/POPC/Chol at 15 and 25°C. By combining two techniques with different spatial sensitivities, namely FRET and small-angle neutron scattering (SANS), we have significantly narrowed the uncertainty in domain size estimates for bSM/POPC/Chol mixtures. Compositional trends in FRET data revealed coexisting domains at 15 and 25°C for both mixtures, while SANS measurements detected no domain formation for bSM/POPC/Chol. Together these results indicate that liquid domains in bSM/POPC/Chol are between 2 and 7nm in radius at 25°C: that is, domains must be on the order of the 2-6nm Förster distance of the FRET probes, but smaller than the ~7nm minimum cluster size detectable with SANS. However, for palmitoyl SM (PSM)/POPC/Chol at a similar composition, SANS detected coexisting liquid domains. This increase in domain size upon replacing the natural SM component (which consists of a mixture of chain lengths) with synthetic PSM, suggests a role for SM chain length in modulating raft size in vivo.
膜筏大小的测量对于理解细胞中膜筏的稳定性和功能至关重要。对于三元模型膜系统鞘磷脂(SM)/1-棕榈酰-2-油酰-sn-甘油-3-磷酸胆碱(POPC)/胆固醇(Chol),其结构域大小的报道差异很大,从纳米到微米不等,这证明了准确测量膜筏大小具有挑战性。利用荧光共振能量转移(FRET)和差示扫描量热法(DSC),我们建立了猪脑SM(bSM)/二油酰-sn-甘油-3-磷酸胆碱(DOPC)/Chol和bSM/POPC/Chol在15℃和25℃时的相图。通过将两种具有不同空间灵敏度的技术,即FRET和小角中子散射(SANS)相结合,我们显著缩小了bSM/POPC/Chol混合物结构域大小估计的不确定性。FRET数据中的成分趋势表明,两种混合物在15℃和25℃时均存在共存结构域,而SANS测量未检测到bSM/POPC/Chol形成结构域。这些结果共同表明,bSM/POPC/Chol中的液滴结构域在25℃时半径为2至7纳米:也就是说,结构域必须在FRET探针2 - 6纳米的Förster距离范围内,但小于SANS可检测到的约7纳米的最小簇尺寸。然而,对于具有相似组成的棕榈酰SM(PSM)/POPC/Chol,SANS检测到共存的液滴结构域。用合成的PSM取代天然SM成分(其由链长混合物组成)后,结构域大小增加,这表明SM链长在体内调节膜筏大小中起作用。