排序方式: 共有113条查询结果,搜索用时 15 毫秒
101.
Dr. Haitao Yu Dr. Angelina Angelova Dr. Borislav Angelov Dr. Brendan Dyett Dr. Lauren Matthews Yiran Zhang Mohamad El Mohamad Xudong Cai Dr. Sepideh Valimehr Prof. Calum J. Drummond Dr. Jiali Zhai 《Angewandte Chemie (International ed. in English)》2023,62(35):e202304977
Ionisable amino-lipid is a key component in lipid nanoparticles (LNPs), which plays a crucial role in the encapsulation of RNA molecules, allowing efficient cellular uptake and then releasing RNA from acidic endosomes. Herein, we present direct evidence for the remarkable structural transitions, with decreasing membrane curvature, including from inverse micellar, to inverse hexagonal, to two distinct inverse bicontinuous cubic, and finally to a lamellar phase for the two mainstream COVID-19 vaccine ionisable ALC-0315 and SM-102 lipids, occurring upon gradual acidification as encountered in endosomes. The millisecond kinetic growth of the inverse cubic and hexagonal structures and the evolution of the ordered structural formation upon ionisable lipid-RNA/DNA complexation are quantitatively revealed by in situ synchrotron radiation time-resolved small angle X-ray scattering coupled with rapid flow mixing. We found that the final self-assembled structural identity, and the formation kinetics, were controlled by the ionisable lipid molecular structure, acidic bulk environment, lipid compositions, and nucleic acid molecular structure/size. The implicated link between the inverse membrane curvature of LNP and LNP endosomal escape helps future optimisation of ionisable lipids and LNP engineering for RNA and gene delivery. 相似文献
102.
Seyed Majid Hashemianzadeh Shirin Faraji Amir Hossein Amin Sepideh Ketabi 《Monatshefte für Chemie / Chemical Monthly》2008,139(2):89-100
Summary. Interactions of the DNA bases adenine (A), guanine (G), cytosine (C), and thymine (T) with various metal ions (M) of groups IA and IIA of the periodic table of the elements were studied at the HF, MP2, and DFT levels of theory. The structures and thermodynamic stabilities of these species were studied at the gas phase. The calculations
uphold that there exist two active sites in G and one in A, C, and T. The calculations also show that the O2 atom in T is a more active site for metal ion bindings than that in C. The stability energies for G … M complexes are larger than those for A … M complexes and the stability energies for T … M complexes are larger than those for C … M complexes. As z/r ratio for the metal ion increases, the interaction energy for the complex increases systematically. Thermodynamic quantities
such as ΔH, ΔG, ΔS, and ln K were determined for each complexation reaction, [Base+M
n+ →(Base … M)
n+]. A, G, and C complexation reactions except for C … Rb+ are exothermic. The situation is quite different for T complexation reactions and all except for T … Be2+ and T … Mg2+ are endothermic. 相似文献
103.
Sepideh Khoee Somayeh Zamani Masoumeh Tajik 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2009,72(5):1054-1061
Several diamines with remarkable different polarities were used to produce photoactive poly(amide–imide)s (PAI)s in a quantitative yield. The absorption, fluorescence and photophysical properties of series of poly(amide–imide)s containing fused aromatic systems as energy donor and energy acceptor with different diamines cores are described. Poly(amide–imide)s exhibit broad fluorescent characteristic, and its fluorescent intensity is related to the intermolecular chain–chain or chain–solvent interaction. The fluorescence spectra confirmed an efficient singlet–singlet energy transfer between fused aromatic systems. The self-quenching mechanism was studied according to the specific behavior of these polymers in different solvents. The self-quenching rate constant for the association reaction in the excited state (Kq) could be measured from the Stern–Volmer equation. The kind of fused system and diamines show different electron migration mechanisms and photoluminescent properties in the singlet-excited states. By using the exothermic energy transfer as a function of diamine polarity, the electron transfer mechanism was evaluated for aromatic poly(amide–imide)s. In principle, the fluorescence energy is absorbed by different (PAI)s and raises the molecules to one of its excited states. Afterwards this excitation energy transfers through the different relaxation channels, i.e. columbic or exchange energy transfer. 相似文献
104.
105.
In this study, a dual wavelength spectrophotometric method was presented on the basis of Cu2+‐NH3 complex decomposition by the citrate ion and the formation of Cu2+‐citrate complex. Sum of the absorbance decreasing at 600 nm (λmax for Cu2+‐NH3 complex) and the absorbance increasing at 750 nm (λmax for Cu2+‐citrate complex) was used in quantification. This method is very selective, fast and inexpensive but relatively less sensitive. The calibration curve is linear in the range of 0.4–8 mmol/L with a detection limit of 0.13 mmol/L. The relative standard deviation (RSD%) for the six repeated determinations (2 mmol/L) is 1.75%. Interference studies of more than twenty common compounds, which are present in the studied samples, were carried out. Only oxalic and ascorbic acids are serious interferes and which interferences were eliminated by simple procedures. Finally, the proposed method was successfully applied in the determination of citric acid content in ORS powder and some fruit juices. 相似文献
106.
Yaser Ghazi Akbar Vaseghi Sepideh Ahmadi Fatemeh Haddadi 《Journal of fluorescence》2018,28(2):633-638
Gene expression analysis is considered to be extremely important in many different biological researches. DNA-based diagnostic test, which contributes to DNA identification, has higher specificity, cost, and speed than some biochemical and molecular methods. In this study, we try to use the novel nano technology approach with Multiplex RT-PCR and Gold nano particular probes (GNPs-probes) in order to get gene expression in Curcumas melons. We used Agrobacterium tumefactions for gene transfer and GUS reporter gene as a reporter. After cDNA synthesis, Multiplex PCR and Multiplex RT-PCR techniques were used. Finally, probes were designed for RNA of GUS and Actin genes, and then the analysis of the gene expression using the probes attached to GNPs was carried out and the color changes in the GNPs were applied. In the following, probes hybridization was checked with DNA between 400 to 700 nm wavelengths and the highest rate was observed in the 550 to 650 nm. The results show that the simultaneous use of GNP-attached detectors and Multiplex RT-PCRcan reduce time and costmore considerably than somelaboratory methods for gene expiration investigation. Additionally, it can be seen thatthere is an increase in sensitivity and specificity of our investigation. Based on our findings, this can bea novel study doneusingMultiplex RT-PCRand unmodified AuNPs for gene transfer and expression detection to plants. We can claim that this assay has a remarkable advantage including rapid, cost-effectiveness, specificity and accuracy to detect transfer and expression genes in plants. Also,we can use this technique from other gene expressionsin many different biology samples. 相似文献
107.
Rahmani Ali Reza Poormohammadi Ali Zamani Fahime Tahmasebi Birgani Yaser Jorfi Sahand Gholizadeh Sepideh Mohammadi Mohammad Javad Almasi Halime 《Research on Chemical Intermediates》2018,44(9):5501-5519
Research on Chemical Intermediates - Due to its high toxicity, phenol is classified as a priority. In this paper, the removal of phenol from aqueous solutions was investigated using EDTA and... 相似文献
108.
Beran GJ Chronister EL Daemen LL Moehlig AR Mueller LJ Oomens J Rice A Santiago-Dieppa DR Tham FS Theel K Yaghmaei S Morton TH 《Physical chemistry chemical physics : PCCP》2011,13(45):20380-20392
Vibrational spectra of the conjugate acid of Me(2)NCH(2)CH(2)CH(2)CH(2)NMe(2) (N,N,N',N'-tetramethylputrescine) have been examined in the gaseous and crystalline phases using Infrared Multiple Photon Dissociation (IRMPD) spectroscopy, Inelastic Neutron Scattering (INS), and high pressure Raman spectroscopy. A band observed near 530 cm(-1) is assigned to the asymmetric stretch of the bridging proton between the two nitrogens, based on deuterium substitution and pressure dependence. The NN distance measured by X-ray crystallography gives a good match to DFT calculations, and the experimental band position agrees with the value predicted from theory using a 2-dimensional potential energy surface. The reduced dimensionality potential energy surface, which treats the ion as though it possesses a linear NHN geometry, shows low barriers to proton transit from one nitrogen to the other, with zero point levels close to the barrier tops. In contrast, two other related systems containing strong hydrogen bonds do not exhibit the same spectroscopic signature of a low barrier hydrogen bond (LBHB). On the one hand, the IRMPD spectra of the conjugate acid ions of the amino acid N,N,N',N'-tetramethylornithine (in which the two nitrogens have different basicities) show fewer bands and no comparable isotopic shifts in the low frequency domain. On the other hand, the IRMPD spectrum of the shorter homologue Me(2)NCH(2)CH(2)CH(2)NMe(2) (N,N,N',N'-tetramethyl-1,3-propanediamine), for which the NHN bond angle deviates substantially from linearity, displays more than one band in the 1100-1400 cm(-1) domain, which vanish as a consequence of deuteration. 相似文献
109.
Seyyed Javad Sabounchei A. R. Dadrass Sepideh Samiee 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):1331-1337
The reaction of the title ylide {PhCOCHP(p-tolyl)3} with Pd(II), Pt(II). Hg(II), and Ag(I) in equimolar ratios using CH3CN, CH3OH, and CH2Cl2 as solvents have yielded [{(p-tolyl)3PCHCOC6H5} PdCl2]2 (I), [{(p-tolyl)3 PCHCOC6H5} PtCl2]2(2), [Hg(NO3)2 {(p-tolyl)3 PCHCOC6H5}](3), and [Ag{(p-tolyl)3 PCHCOC6H5 < eqid1 > 2]+ (4). The IR, 1H 13C, and 31P NMR together with micro analysis data of the products were obtained. 相似文献
110.
Sepideh Sharif Dr. Richard P. Rucker Dr. Nalin Chandrasoma Dr. David Mitchell Dr. Michael J. Rodriguez Dr. Robert D. J. Froese Prof. Michael G. Organ 《Angewandte Chemie (International ed. in English)》2015,54(33):9507-9511
A single set of reaction conditions for the palladium‐catalyzed amination of a wide variety of (hetero)aryl halides using primary alkyl amines has been developed. By combining the exceptionally high reactivity of the Pd‐PEPPSI‐IPentCl catalyst (PEPPSI=pyridine enhanced precatalyst preparation, stabilization, and initiation) with the soluble and nonaggressive sodium salt of BHT (BHT=2,6‐di‐tert‐butyl‐hydroxytoluene), both six‐ and five‐membered (hetero)aryl halides undergo efficient and selective amination. 相似文献