Maleimide-Functionalized Thiol Reactive Copolymer Brushes: Fabrication and Post-Polymerization Modification

Polymer brushes that present side chain functional reactive groups are attractive platforms for the development of functional surface coatings. From the wide spectrum of possible postpolymerization modification reactions, thiol-based conjugation chemistries are particularly appealing as they can be performed reagent-less under mild conditions and can allow the site-selective conjugation of biomolecules. This manuscript reports a direct approach for the preparation of maleimide-functionalized polymer brushes. These brushes were obtained by surface-initiated atom transfer radical copolymerization of poly(ethylene glycol) methacrylate and a furan-protected, maleimide containing monomer, followed by a thermally induced retro DielsAlder reaction to unmask the maleimide groups. The feasibility of these brushes to serve as a platform for postpolymerization functionalization was explored in a series of model experiments using a variety of low molecular weight thiols, including a fluorescent dye and a thiol-modified biotin-derivative. The biotinylated brushes were subsequently used for the immobilization of streptavidin-coated quantum-dots. The copolymer brushes presented in this manuscript are attractive since they combine the nonbiofouling properties of the poly(ethylene glycol) methacrylate monomer with the chemoselective reactivity of the maleimide containing monomer, which makes them an attractive platform, e.g., for the immobilization of biomolecules

Inhibition of glycogen synthase kinase-3 beta reduces ROS production and alters antioxidant enzyme activities in MPP plus -induced neuronal cell death

OCC World Congress / Annual SFRR-E Conference -- JUN 21-23, 2017 -- Berlin, GERMANYWOS: 000403716100099OCC, SFRR-ETUBITAK (The Scientific and Technical Research Council of Turkey)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [215S528]; Ege University Scientific Research FoundationEge University [15-ECZ-012]This study was supported by TUBITAK (The Scientific and Technical Research Council of Turkey) (Project Number: 215S528) and the Ege University Scientific Research Foundation (Project Number: 15-ECZ-012)

Design, Synthesis, and Biological Evaluation of Novel Tomentosin Derivatives in NMDA-Induced Excitotoxicity

N-methyl-D-aspartate (NMDA) receptor stimulation may lead to excitotoxicity, which triggers neuronal death in brain disorders. In addition to current clinical therapeutic approaches, treatment strategies by phytochemicals or their derivatives are under investigation for neurodegenerative diseases. In the present study, novel amino and 1,2,3-triazole derivatives of tomentosin were prepared and tested for their protective and anti-apoptotic effects in NMDA-induced excitotoxicity. Amino-tomentosin derivatives were generated through a diastereoselective conjugate addition of several secondary amines to the alpha-methylene-gamma-butyrolactone function, while the 1,2,3-triazolo-tomentosin was prepared by a regioselective Michael-type addition carried out in the presence of trimethylsilyl azide (TMSN3) and the alpha-methylene-gamma-lactone function. The intermediate key thus obtained underwent 1,3-dipolar Huisgen cycloaddition using a wide range of terminal alkynes. The possible effects of the derivatives on cell viability and free-radical production following NMDA treatment were measured by Water-Soluble Tetrazolium Salts (WST-1) and Dichlorofluorescein Diacetate (DCF-DA) assays, respectively. The alterations in apoptosis-related proteins were examined by Western blot technique. Our study provides evidence that synthesized triazolo- and amino-tomentosin derivatives show neuroprotective effects by increasing cellular viability, decreasing ROS production, and increasing the Bcl-2/Bax ratio in NMDA-induced excitotoxicity. The findings highlight particularly 2e, 2g, and 6d as potential regulators and neuroprotective agents in NMDA overactivation.Region Centre, France through the ValPAMMeT Program with the Meknes-Tafilalet area of MoroccoThis research was supported by the Region Centre, France through the ValPAMMeT Program with the Meknes-Tafilalet area of Morocco

EFFECTS OF GENETIC VARIATIONS OF MLCK2, AMPD1, AND COL5A1 ON MUSCLE ENDURANCE

Introduction: Although potential relationships with genetic variants of MLCK2, AMPD1 and COL5A1 have been detected in molecular studies evaluating sports performance from the genetic perspective, there are limited data in terms of muscle endurance and physical fitness. Materials and Methods:This study aimed to evaluate these variants in terms of lower limb muscle endurance and physical fitness in thirty-three soccer players. Genotypes were determined by High Resolution Melting (HRM) analysis in qPCR after genomic DNA was isolated from buccal swab samples from the participants. Measurements of lower limb muscle endurance, the dynamic leap and balance test (DLBT), and the standing broad jump test (SBJ) were taken for all the participants. Results: Greater height (p = 0.006), higher DLBT (p = 0.016) and SBJ (p = 0.033) scores, as well as greater left hip adduction (p <0.001), were detected in those with the CT genotype for AMPD1 as compared to those with CC. For MLCK rs28497577, it was found that the players carrying the AA genotype were taller (p = 0.046), heavier (p = 0.049), and had greater left knee extension (p=0.014) and left foot plantar flexion (p =0.040) than those carrying the C allele.Those with the CT genotype for COL5A1 rs12722 had greater right hip extension (p = 0.040) and right knee extension (p = 0.048) than those with the CC genotype. Conclusions: Our results showed that MLCK2 and COL5A1 gene variants are associated with body composition and lower limb muscle endurance, and the presence of the AMPD1 CT genotype may contribute positively to balance, correct positioning, controlled strength, and hip mobility. Evidence level II; Comparative prospective study

The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice

Background The genetic and epidemiological features of hereditary ataxias have been reported in several populations; however, Turkey is still unexplored. Due to high consanguinity, recessive ataxias are more common in Turkey than in Western European populations