NBD荧光探针对含POPC和DPPC模型膜的影响。

Q3 Biochemistry, Genetics and Molecular Biology Molecular Membrane Biology Pub Date : 2016-03-01 Epub Date: 2016-07-25 DOI:10.1080/09687688.2016.1185175
Chi-Jung Weng, Ju-Ping Wu, Ming-Yen Kuo, Ya-Wei Hsueh
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引用次数: 5

摘要

为了研究荧光探针对膜性能的影响,我们研究了在存在和不存在荧光探针的情况下,由1,2-双棕榈酰- n-甘油-3-磷酸胆碱(DPPC)和1-棕榈酰- 2-油基- n-甘油-3-磷酸胆碱(POPC)组成的模型膜。以NBD-DOPE或C6-NBD-PC为探针,用荧光显微镜观察了巨型单层囊泡(GUVs)的形态与温度和组成的关系。采用2H-NMR研究了不含荧光探针的模型膜的相行为。我们发现在guv上观察到的亮相是富含POPC的流体相,暗相是富含DPPC的凝胶相。当guv处于凝胶+流体共存状态时,NBD-DOPE和C6-NBD-PC优先参与液相域。两种荧光探针(1 mol%)的加入降低了POPC/DPPC膜的转变温度。此外,C6-NBD-PC比NBD-DOPE的作用更强,这可能与荧光分子的结构有关。
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The influence of NBD fluorescent probe on model membranes containing POPC and DPPC.

To investigate the effect of fluorescent probe on the properties of membranes, we studied model membranes composed of 1,2- dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and 1-palmitoyl 2-oleoyl-sn-glycero-3-phosphocholine (POPC) in the presence and absence of fluorescent probe. The morphology of giant unilamellar vesicles (GUVs) has been observed as a function of temperature and composition by fluorescence microscopy using NBD-DOPE or C6-NBD-PC as the probe. The phase behavior of model membranes containing no fluorescent probe was investigated by 2H-NMR spectroscopy. We found that the bright phase observed on GUVs was the fluid phase enriched in POPC and the dark phase was the gel phase enriched in DPPC. NBD-DOPE and C6-NBD-PC preferentially participated in the fluid-phase domains when GUVs were in the gel + fluid phase coexistence. Inclusion of both fluorescent probes (1 mol%) lowered the transition temperature of POPC/DPPC membranes. In addition, C6-NBD-PC exhibited a stronger effect than NBD-DOPE, which was considered to be associated with the structures of fluorescent molecules.

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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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