scholarly journals Morphological Estimation of DMPC/DHPC Self-Assemblies in Diluted Condition: Based on Physicochemical Membrane Properties

Author(s):  
Shogo Taguchi ◽  
Keishi Suga ◽  
Keita Hayashi ◽  
Yukihiro Okamoto ◽  
Hidemi Nakamura ◽  
...  

Self-assembly membranes, composed of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and 1,2-dihexanoyl-sn-glycero-3-phosphocholine (DHPC), were characterized at the total lipid concentration below 20 mM. The sizes of the assemblies varied depending on the molar ratio of DMPC and DHPC (q = [DMPC]/[DHPC]). The small assemblies with diameter of ca. 10 nm were formed at q ≤ 2.0 at 20 ºC (below phase transition temperature of DMPC). The physicochemical membrane properties were then studied using fluorescence probes, 1,6-diphenyl-1,3,5-hexatriene and 6-dodecanoyl-N,N-dimethyl-2-naphthylamine, upon the dilution. DHPC micelle showed a higher membrane fluidity, while the DMPC/DHPC membranes at q ≥ 0.5 showed lower membrane fluidities as well as DMPC vesicle in gel (ordered) phase. Upon dilution, the ordered membrane properties were maintained while the solution turbidities increased, implying the morphological change of the self-assembly, bicelle to the vesicle in gel phase. Based on the obtained results, a phase diagram of DMPC/DHPC binary system (at 20 ºC) is described: (i) the bicelle suspension is transparent and the membrane is in ordered state, (ii) the micelle suspension is transparent and the membrane is in disordered state, (iii) the vesicle suspension is turbid and the membrane is in ordered state.

Molecules ◽  
2019 ◽  
Vol 24 (6) ◽  
pp. 1084 ◽  
Author(s):  
Shaoming Jin ◽  
Zhongyao Du ◽  
Pengjie Wang ◽  
Huiyuan Guo ◽  
Hao Zhang ◽  
...  

Folic acid has been widely introduced into nano-drug delivery systems to give nanoparticle-targeted characteristics. However, the poor water solubility of folic acid may hinder the exploitation of its ability to load antineoplastic drugs. In the present study, we designed a new folate derivative (FA-2-DG) synthesized from folic acid and 2-Deoxyglucose (2-DG). The aim of this study was to evaluate the self-assembly characteristics of FA-2-DG, and its ability of loading cisplatin. The critical micelle concentration was 7.94 × 10−6 mol L−1. Fourier transform infrared spectroscopy indicated that hydrogen bonding interaction is a main driving force for the self–assembly of FA-2-DG. The particle was stable in pure water or 0.5% bovine serum albumin dispersions. By forming a coordination bond, the particles assembled from FA-2-DG can load cisplatin. The loading efficiency was maximal when the molar ratio of FA-2-DG to cisplatin was 2:1.


RSC Advances ◽  
2016 ◽  
Vol 6 (63) ◽  
pp. 58160-58172 ◽  
Author(s):  
Y. Chen ◽  
Y. X. Zhang ◽  
Z. F. Wu ◽  
X. Y. Peng ◽  
T. Su ◽  
...  

The self-assembly and drug release of the three PEG–PCL copolymers with different topologies but identical molar ratio between PEG to PCL.


Author(s):  
R. Hutterer ◽  
M. Hof

The emission behaviour of the two polarity sensitive probes Prodan and Patman in phospholipid vesicles was studied as a function of the concentration of ethanol. Comparing the spectral shifts in both the symmetric lipid 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC) showing a phase transition from a normal to a fully interdigitated gel phase and the strongly asymmetric lipid 1-stearoyl-2-lauroyl-sn-glycero-3-phosphatidylcholine (C(18):C(12)-PC) favouring a mixed interdigitated gel phase we show that the huge red shifts of Prodan in presence of higher ethanol concentrations cannot be easily attributed to a specific lipid phase transition. Rather, probe relocation and a pronounced increase in solvent relaxation (SR) as monitored by time-resolved emission spectra (TRES) in presence of ethanol contribute to the large shifts observable in both lipid systems in case of Prodan. While Patman exhibits a red shift caused by increased SR due to the ethanol induced formation of a fully interdigitated phase in DPPC, hardly any shift occurs in C(18):C(12)-PC, which is supposed not to undergo an ethanol-induced phase transition.


2018 ◽  
Vol 2 (4) ◽  
pp. 73 ◽  
Author(s):  
Shogo Taguchi ◽  
Keishi Suga ◽  
Keita Hayashi ◽  
Yukihiro Okamoto ◽  
Ho-Sup Jung ◽  
...  

Self-assemblies composed of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and 1,2-dihexanoyl-sn-glycero-3-phosphocholine (DHPC) form several kinds of structures, such as vesicle, micelle, and bicelle. Their morphological properties have been studied widely, but their interfacial membrane properties have not been adequately investigated. Herein, we report a systematic characterization of DMPC/DHPC assemblies at 20 °C. To investigate the phase behavior, optical density OD500, size (by dynamic light scattering), membrane fluidity 1/PDPH (using 1,6-diphenyl-1,3,5-hexatriene), and membrane polarity GP340 (using 6-dodecanoyl-N,N-dimethyl-2-naphthylamine) were measured as a function of molar ratio of DHPC (XDHPC). Based on structural properties (OD500 and size), large and small assemblies were categorized into Region (i) (XDHPC < 0.4) and Region (ii) (XDHPC ≥ 0.4), respectively. The DMPC/DHPC assemblies with 0.33 ≤ XDHPC ≤ 0.67 (Region (ii-1)) showed gel-phase-like interfacial membrane properties, whereas DHPC-rich assemblies (XDHPC ≥ 0.77) showed disordered membrane properties (Region (ii-2)). Considering the structural and interfacial membrane properties, the DMPC/DHPC assemblies in Regions (i), (ii-1), and (ii-2) can be determined to be vesicle, bicelle, and micelle, respectively.


2002 ◽  
Vol 724 ◽  
Author(s):  
Chrystelle S. Cazalis ◽  
Vincent P. Conticello

AbstractSpider dragline silk fiber displays a unique and technologically significant combination of high tensile and compressive strength. The structural origin of these properties arises from the alternating sequence of crystalline alanine-rich domains and amorphous glycine-rich domains, which undergo microscopic phase separation in the silk fiber. We previously reported the synthesis and the self-assembly of a novel polypeptide 1, which emulates the modular structure of crystalline and amorphous elastomeric domains in dragline silk proteins. The sequence of this polypeptide comprises an alternating arrangement of a self-complementary, amphiphilic silk-mimetic oligopeptide (Ala-Glu-Ala-Glu-Ala-Lys-Ala-Lys) and environmentally-responsive elastin-mimetic segment (Val-Pro-Gly-Val-Gly). We report herein the synthesis and the self-assembly of an analogous polypeptide (2) with an higher content of elastin mimetic pentapeptides. A synthetic gene encoding four repeats of the alternating sequence was expressed in E. coli strain BL21(DE3) as a C-terminal fusion to a decahistidine leader sequence to afford a polypeptide with a molar mass of approximately 39 kDa. The regularly alternating pattern of elastin-mimetic and silk-mimetic blocks within the protein allowed the copolymer to spontaneously self-assemble upon heating above the phase transition of the elastin-mimetic block. The self-assembly process was studied using a combination of CD and solid-state NMR spectroscopy, which suggested that the alanine-rich domains undergo a conformational rearrangement from α-helix to β-sheet. This rearrangement coincides with the macromolecular phase transition of the elastin-mimetic domains, which resulted in irreversible aggregation of the polypeptide above the Tt of the elastin-mimetic domains.


Soft Matter ◽  
2011 ◽  
Vol 7 (1) ◽  
pp. 110-117 ◽  
Author(s):  
William Edwards ◽  
Cecile A. Lagadec ◽  
David K. Smith

2018 ◽  
Vol 510 ◽  
pp. 133-141 ◽  
Author(s):  
Audrey Arnould ◽  
Fabrice Cousin ◽  
Léa Chabas ◽  
Anne-Laure Fameau

2012 ◽  
Vol 84 (12) ◽  
pp. 2569-2578 ◽  
Author(s):  
Chunhui Luo ◽  
Chongyi Chen ◽  
Zhibo Li

A new type of hetero-grafted molecular bottlebrush with polypeptide as backbone was synthesized using graft-onto strategy. Poly(γ-propargyl-L-glutamate) (PPLG) as backbone was firstly synthesized via ring-opening polymerization (ROP) of γ-propargyl-L-glutamate (PLG) N-carboxyanhydride (NCA). Next, polystyrene-N3 (PS-N3) and monomethoxy poly(ethylene glycol)-N3 (mPEG-N3) as side chains were grafted onto the PPLG backbone using copper-catalyzed click reaction, which afforded good grafting density and efficiency. Two polypeptide bottlebrushes with PS-to-mPEG molar ratio at 70/30 and 30/70 were prepared. The self-assembly behaviors of these two polypeptide bottlebrushes were investigated using the cosolvent method, and their supramolecular structures were characterized using light scattering (LS) and electron microscopy.


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