Search results for "Sarcosine"

showing 10 items of 26 documents

Polymeric Nanoparticles with Neglectable Protein Corona

2020

Small : nano micro 16(18), 1907574 (2020). doi:10.1002/smll.201907574

540 Chemistry and allied sciencesDispersity610 Medizinmicellar structuresNanoparticleProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsBiomaterialschemistry.chemical_compoundAdsorption610 Medical sciencesHumansGeneral Materials ScienceParticle SizeGel electrophoresisChemistryasymmetrical flow field-flow fractionationSarcosineGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineering540 Chemiedrug deliveryNanoparticlesParticleProtein CoronaParticle sizePeptides0210 nano-technologyHydrophobic and Hydrophilic InteractionsEthylene glycolBiotechnologySmall
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Efficient Shielding of Polyplexes Using Heterotelechelic Polysarcosines

2018

Shielding agents are commonly used to shield polyelectrolyte complexes, e.g. polyplexes, from agglomeration, precipitation in complex media, like blood, and thus enhance their circulation times in vivo. Since up to now primarily poly(ethylene glycol) (PEG) has been investigated to shield non-viral carriers for systemic delivery, we report on the use of polysarcosine (pSar) as a potential alternative for steric stabilization. A redox-sensitive, cationizable lipo-oligomer structure (containing two cholanic acids attached via a bioreducible disulfide linker to an oligoaminoamide backbone in T-shape configuration) was equipped with azide-functionality by solid phase supported synthesis. After m…

BiodistributionPolymers and Plastics02 engineering and technologypolysarcosine010402 general chemistry01 natural sciencesArticlelcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPEG rationucleic acid carrierbiodistributionlipopolyplexshielding agentclick-chemistryGeneral Chemistry021001 nanoscience & nanotechnologyPolyelectrolyte0104 chemical scienceschemistryPolymerizationClick chemistryBiophysicsSurface modification0210 nano-technologyEthylene glycolLinkerbiomaterials
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Glycine receptors influence radial migration in the embryonic mouse neocortex.

2011

To investigate whether glycine receptors influence radial migration in the neocortex, we analyzed the effect of glycine and the glycinergic antagonist strychnine, on the distribution of 5-bromo-2'deoxyuridine-labeled neurons in organotypic slice cultures from embryonic mice cortices. Application of glycine impeded radial migration only in the presence of the glycine-transport blockers, ALX-5407 and ALX-1393. This effect was blocked by the specific glycine receptor antagonist strychnine, whereas application of strychnine in the absence of glycine was without effect. We conclude from these observations that an activation of glycine receptors can impede radial migration, but that the glycinerg…

GlycineCell CountNeocortexBiologychemistry.chemical_compoundMiceOrgan Culture TechniquesReceptors GlycineCell MovementGlial Fibrillary Acidic ProteinmedicineAnimalsDrug InteractionsReceptorGlycine receptorNeuronsNeocortexGeneral NeuroscienceAntagonistGlycine AgentsSarcosineGlycine receptor antagonistStrychnineStrychnineEmbryo MammalianCell biologymedicine.anatomical_structurechemistryBromodeoxyuridineCerebral cortexPhosphopyruvate HydrataseGlycineNeuroscienceNeuroreport
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PeptoSomes for Vaccination: Combining Antigen and Adjuvant in Polypept(o)ide-Based Polymersomes.

2017

In this work, the first vaccine is reported based on a PeptoSome, which contains a model antigen (SIINFEKL) and adjuvant (CpG). PeptoSomes are polypept(o)ide-based polymersomes built of a block-copolymer with polysarcosine (PSar) as the hydrophilic block (X n = 111) and poly(benzyl-glutamic acid) (PGlu(OBn)) as the hydrophobic one (X n = 46). The polypept(o)ide is obtained with low dispersity index of 1.32 by controlled ring-opening polymerization. Vesicle formation by dual centrifugation technique allows for loading of vesicles up to 40 mol%. PeptoSomes are characterized by multiangle dynamic light scattering, static light scattering, and cryogenic transmission electron microscopy (cryoTEM…

Hydrodynamic radiusPolymers and Plasticsmedicine.medical_treatmentT-LymphocytesDispersityGene ExpressionBioengineeringchemical and pharmacologic phenomenaBone Marrow Cells02 engineering and technology010402 general chemistryLymphocyte Activation01 natural sciencesBiomaterialsPeptoidsDynamic light scatteringAntigenAdjuvants ImmunologicMaterials ChemistrymedicineHumansStatic light scatteringAntigensVaccinesChemistryVesicleVaccinationSarcosineDendritic Cells021001 nanoscience & nanotechnologyMolecular biologyCoculture Techniques0104 chemical sciencesOligodeoxyribonucleotidesPolymersomeB7-1 AntigenCytokinesB7-2 Antigen0210 nano-technologyPeptidesAdjuvantBiomarkersBiotechnologyMacromolecular bioscience
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Choline Metabolism and Risk of Atrial Fibrillation and Heart Failure in the PREDIMED Study

2020

Abstract Background Few studies have examined the associations of trimethylamine-N-oxide (TMAO) and its precursors (choline, betaine, dimethylglycine, and L-carnitine) with the risk of atrial fibrillation (AF) and heart failure (HF). This study sought to investigate these associations. Methods Prospective associations of these metabolites with incident AF and HF were examined among participants at high cardiovascular risk in the PREDIMED study (PREvención con DIeta MEDiterránea) after follow-up for about 10 years. Two nested case-control studies were conducted, including 509 AF incident cases matched to 618 controls and 326 HF incident cases matched to 426 controls. Plasma levels of TMAO an…

Malemedicine.medical_specialtyClinical BiochemistryTrimethylamine N-oxide030204 cardiovascular system & hematologyGastroenterologyCholineDimethylglycineMethylamines03 medical and health scienceschemistry.chemical_compound0302 clinical medicineBetaineRisk FactorsCarnitineInternal medicineAtrial FibrillationmedicineHumansCholineProspective Studies030212 general & internal medicineAgedHeart Failurebusiness.industryBiochemistry (medical)SarcosineAtrial fibrillationArticlesOdds ratiomedicine.diseaseBetainechemistryQuartileCase-Control StudiesHeart failureFemalebusinessClinical Chemistry
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4,5-Disubstituted 1-Methylimidazoles via Cyclization of Defined α-Aminoketones: Synthesis of Fungerin and Analogues I

2016

A protocol for the chemoselective synthesis of the fungal metabolite fungerin has been developed. First the required N-methyl α-aminoketone was generated starting from sarcosine, propiolic acid, and prenyl bromide. Marckwald thioimidazole cyclization and subsequent sulfur removal delivered the target fungerin as well as an analogue, respectively, displaying defined substitution patterns.

Natural productSarcosinePropiolic acid010405 organic chemistryStereochemistryOrganic Chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesSulfurCatalysis0104 chemical scienceschemistry.chemical_compoundFungal metabolitechemistryPrenylationBromideImidazoleSynthesis
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Impact of compatible solutes on the mechanical properties of fibronectin: a single molecule analysis

2003

The influence of ectoine and sarcosine on the mechanical properties of surface bound fibronectin has been investigated by means of force microscopy. Single molecule stretching experiments of fibronectin molecules reveal that ectoine and sarcosine increase the tendency of the polypeptide to coil, thus decreasing its apparent persistence length. This behavior can be explained by means of the preferential exclusion model implying that the osmolytes are expelled from the protein surface due to the increase in chemical potential of the denatured, i.e. stretched, state forcing the protein into a more compact structure. Detailed analysis of the unfolding forces, which are extracted from the succes…

Persistence lengthSarcosinebiologyChemistryStereochemistryGeneral Physics and AstronomyEctoineFibronectinchemistry.chemical_compoundOsmolytebiology.proteinBiophysicsMoleculeOsmoprotectantPhysical and Theoretical ChemistrySurface proteinPhysical Chemistry Chemical Physics
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Polypept(o)ides: Hybrid Systems Based on Polypeptides and Polypeptoids.

2015

Polypept(o)ides combine the multifunctionality and intrinsic stimuli-responsiveness of synthetic polypeptides with the "stealth"-like properties of the polypeptoid polysarcosine (poly(N-methyl glycine)). This class of block copolymers can be synthesized by sequential ring opening polymerization of α-amino acid N-carboxy-anhydrides (NCAs) and correspondingly of the N-substituted glycine N-carboxyanhydride (NNCA). The resulting block copolymers are characterized by Poisson-like molecular weight distributions, full end group integrity, and dispersities below 1.2. While polysarcosine may be able to tackle the currently arising issues regarding the gold standard PEG, including storage diseases i…

Polymers and PlasticsChemistryPolysarcosineOrganic ChemistryGene Transfer TechniquesSarcosineCombinatorial chemistryRing-opening polymerizationProtein Structure SecondaryAnhydridesPolymerizationMolecular WeightEnd-groupPeptoidsDrug Delivery SystemsNanomedicineHybrid systemMaterials ChemistryCopolymerNanomedicineHumansAmino AcidsPeptidesProtein secondary structureMacromolecular rapid communications
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Synthesis and Sequential Deprotection of Triblock Copolypept(o)ides Using Orthogonal Protective Group Chemistry

2014

The synthesis of triblock copolymers based on polysarcosine, poly-N-ε-t-butyloxycarbonyl-l-lysine, and poly-N-ε-t-trifluoroacetyl-l-lysine by ring-opening polymerization of the corresponding α-amino acid N-carboxyanhydrides (NCAs) is described. For the synthesis of N-ε-t-butyloxycarbonyl-l-lysine (lysine(Boc)) NCAs, an acid-free method using trimethylsilylchloride/triethylamine as hydrochloric acid (HCl) scavengers is presented. This approach enables the synthesis of lysine(Boc) NCA of high purity (melting point 138.3 °C) in high yields. For triblock copolypept(o)ides, the degree of polymerization (Xn ) of the polysarcosine block is varied between 200 and 600; poly-N-ε-t-butyloxycarbonyl-l-…

Polymers and PlasticsOrganic ChemistryLysineSarcosineHydrochloric acidDegree of polymerizationcomplex mixturesPolymerizationchemistry.chemical_compoundEnd-groupchemistryPolymerizationPolymer chemistryMaterials ChemistryMelting pointCopolymerbacteriaPolylysinePeptidesTriethylamineMacromolecular Rapid Communications
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Impact of Branching on the Solution Behavior and Serum Stability of Starlike Block Copolymers.

2019

The size control of nanomedicines for tumor diagnosis and therapy is of high importance, since it enables or disables deep and sufficient tumor penetration. Amphiphilic star-shaped block copolypept(o)ides offer substantial promise to precisely adjust the hydrophobic core and the hydrophilic corona, independent of each other, and therefore simultaneously control the size dimension in the interesting size range from 10 to 30 nm. To gain access to core-shell structures of such sizes, 3-arm and 6-arm PeptoStars, based on poly(gamma-tert-butyloxycarbonyl-L-glutamate)-b-polysarcosine (pGlu(OtBu)-b-pSar), were prepared via controlled living ring-opening polymerization (ROP) of the corresponding N-…

Protein Conformation alpha-HelicalMaterials sciencePolymers and PlasticsPolysarcosineSize-exclusion chromatographyBioengineering02 engineering and technology010402 general chemistryBranching (polymer chemistry)01 natural sciencesPolymerizationBiomaterialsPlasmaAmphiphileMaterials ChemistryCopolymerHumanschemistry.chemical_classificationMolecular massSarcosinePolymer021001 nanoscience & nanotechnology0104 chemical sciencesPolymerizationchemistryChemical engineeringNanoparticlesProtein Corona0210 nano-technologyPeptidesOligopeptidesBiomacromolecules
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