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41.
Interaction of PiB‐Derivative Metal Complexes with Beta‐Amyloid Peptides: Selective Recognition of the Aggregated Forms 下载免费PDF全文
Dr. André F. Martins David M. Dias Dr. Jean‐François Morfin Dr. Sara Lacerda Dr. Douglas V. Laurents Dr. Éva Tóth Prof. Carlos F. G. C. Geraldes 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(14):5413-5422
Metal complexes are increasingly explored as imaging probes in amyloid peptide related pathologies. We report the first detailed study on the mechanism of interaction between a metal complex and both the monomer and the aggregated form of Aβ1–40 peptide. We have studied lanthanide(III) chelates of two PiB‐derivative ligands (PiB=Pittsburgh compound B), L1 and L2, differing in the length of the spacer between the metal‐complexing DO3A macrocycle (DO3A= 1,4,7,10‐tetraazacyclododecane‐1,4,7‐triacetic acid) and the peptide‐recognition PiB moiety. Surface plasmon resonance (SPR) and saturation transfer difference (STD) NMR spectroscopy revealed that they both bind to aggregated Aβ1–40 (KD=67–160 μM ), primarily through the benzothiazole unit. HSQC NMR spectroscopy on the 15N‐labeled, monomer Aβ1–40 peptide indicates nonsignificant interaction with monomeric Aβ. Time‐dependent circular dichroism (CD), dynamic light scattering (DLS), and TEM investigations of the secondary structure and of the aggregation of Aβ1–40 in the presence of increasing amounts of the metal complexes provide coherent data showing that, despite their structural similarity, the two complexes affect Aβ fibril formation distinctly. Whereas GdL1, at higher concentrations, stabilizes β‐sheets, GdL2 prevents aggregation by promoting α‐helical structures. These results give insight into the behavior of amyloid‐targeted metal complexes in general and contribute to a more rational design of metal‐based diagnostic and therapeutic agents for amyloid‐ associated pathologies. 相似文献
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We use recent work on spectral synthesis in multiplier algebras to give an intrinsic characterization of the separable C*-algebras A for which Orc(M(A)) = 1, i.e., for which the relation of inseparability on the topological space of primitive ideals of the multiplier algebra M(A) is an equivalence relation. This characterization has applications to the calculation of norms of inner derivations and other elementary operators on A and M(A). For example, we give necessary and sufficient conditions on the ideal structure of a separable C*-algebra A for the norm of every inner derivation to be twice the distance of the implementing element to the centre of M(A). 相似文献
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Kimberley L. Anderson Wigen Nazarov Christopher S. A. Musgrave Nick Bazin Douglas Faith 《Journal of Radioanalytical and Nuclear Chemistry》2014,299(2):969-975
PolyHIPE foams with densities of 0.05–0.1 g cm?3 have been prepared by the polymerisation of the continuous phase of high internal phase emulsions (HIPEs). The internal aqueous phase in HIPE occupies more than 74 % of the total volume, which leads to highly porous and open-cell morphologies. In this paper a method of preparing polyHIPE foams by using reversible addition-fragmentation chain transfer (RAFT) polymerisation has been investigated. Polystyrene-co-polymethyl methacrylate (PS-co-PMMA) has been studied and by using a variety of characterisation methods, it was possible to compare the polyHIPEs prepared by the conventional free radical polymerisation (FRP) to those by RAFT polymerisation. Scanning electron microscopy images have confirmed the presence of a cellular polyHIPE structure. PS-co-PMMA polyHIPEs made by RAFT have significantly narrower molecular weight distribution with values for the polydispersity index (PDI) for PS-co-PMMA between 1.46 and 2.08 compared to 4.68 observed by FRP. The effects of different concentrations of the RAFT agent on structure, glass transition temperature (T g) and PDI of PS-co-PMMA polyHIPE foams are presented. 相似文献
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Kevin M. Szkop Dr. Andrew R. Jupp Hlib Razumkov Maotong Xu Prof. Dr. Douglas W. Stephan 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(43):10084-10087
The phosphaketene Ph3GePCO is shown to react with the phosphide KP(tBu)2 to generate the anion [Ph3GePC(O)P(tBu)2]− 1 . This species reacts with CH3I or ClGePh3 to give the dissymmetric diphospha-ureas (tBu)2PC(O)P(GePh3)(CH3) 2 and (Ph3Ge)2PC(O)P(tBu)2 3 respectively. Sequential treatment of 2 with a base and CH3I affords a route to (tBu)2PC(O)P(CH3)2 5 . These species are products of the first modular diphospha-urea synthesis. The subsequent thermal and photochemical reactivity of these species was also probed and described. 相似文献
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Christopher L. Douglas 《Communications in Mathematical Physics》2013,319(2):395-423
We compute the fusion rings of positive energy representations of the loop groups of the simple, simply connected Lie groups. 相似文献