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Solution nuclear magnetic resonance structure and molecular dynamics simulations of a murine 18.5 kDa myelin basic protein segment (S72-S107) in association with dodecylphosphocholine micellesMyelStones: the executive roles of myelin basic protein in myelin assembly and destabilization in multiple sclerosis.The proline-rich region of 18.5 kDa myelin basic protein binds to the SH3-domain of Fyn tyrosine kinase with the aid of an upstream segment to form a dynamic complex in vitro.Induced secondary structure and polymorphism in an intrinsically disordered structural linker of the CNS: solid-state NMR and FTIR spectroscopy of myelin basic protein bound to actin.Oxidation of low-density lipoprotein by hemoglobin-hemichrome.Structured functional domains of myelin basic protein: cross talk between actin polymerization and Ca(2+)-dependent calmodulin interactionFuzzy complexes of myelin basic protein: NMR spectroscopic investigations of a polymorphic organizational linker of the central nervous system.In vitro study of the direct effect of extracellular hemoglobin on myelin components.Correlation of geographic distributions of haptoglobin alleles with prevalence of multiple sclerosis (MS) - a narrative literature review."Back to the future" or iron in the MS brain - commentary on "perivascular iron deposits are associated with protein nitration in cerebral experimental autoimmune encephalomyelitis".Over-expression in E. coli and purification of functional full-length murine small C-terminal domain phosphatase (SCP1, or Golli-interacting protein).Phosphorylation of Thellungiella salsuginea dehydrins TsDHN-1 and TsDHN-2 facilitates cation-induced conformational changes and actin assembly.Substitutions mimicking deimination and phosphorylation of 18.5-kDa myelin basic protein exert local structural effects that subtly influence its global folding.Myelin basic protein is a glial microtubule-associated protein -- characterization of binding domains, kinetics of polymerization, and regulation by phosphorylation and a lipidic environment.Thermodynamic analysis of the disorder-to-α-helical transition of 18.5-kDa myelin basic protein reveals an equilibrium intermediate representing the most compact conformation.Solid-state NMR spectroscopy of membrane-associated myelin basic protein--conformation and dynamics of an immunodominant epitope.Misincorporation of the proline homologue Aze (azetidine-2-carboxylic acid) into recombinant myelin basic protein.Divalent cations induce a compaction of intrinsically disordered myelin basic protein.Mechanism of low-density lipoprotein oxidation by hemoglobin-derived iron.Haptoglobin phenotypes differ in their ability to inhibit heme transfer from hemoglobin to LDL.Expression and purification of the active variant of recombinant murine Golli-interacting protein (GIP)--characterization of its phosphatase activity and interaction with Golli-BG21.Proton detection for signal enhancement in solid-state NMR experiments on mobile species in membrane proteins.Potential role of ferric hemoglobin in MS pathogenesis: Effects of oxidative stress and extracellular methemoglobin or its degradation products on myelin components.The interaction of zinc with membrane-associated 18.5 kDa myelin basic protein: an attenuated total reflectance-Fourier transform infrared spectroscopic study.Cardiolipin exposure on the outer mitochondrial membrane modulates α-synuclein.Regulatory effect of the glial Golli-BG21 protein on the full-length murine small C-terminal domain phosphatase (SCP1, or Golli-interacting protein).Nitration of microtubules blocks axonal mitochondrial transport in a human pluripotent stem cell model of Parkinson's disease.Purification and spectroscopic characterization of the recombinant BG21 isoform of murine golli myelin basic protein.Hemoglobin as a source of iron overload in multiple sclerosis: does multiple sclerosis share risk factors with vascular disorders?The BG21 Isoform of Golli Myelin Basic Protein Is Intrinsically Disordered with a Highly Flexible Amino-Terminal Domain†Vascular damage by unstable hemoglobins: the role of heme-depleted globinLyme Disease Frontiers: Reconciling Borrelia Biology and Clinical Conundrums
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P50
description
researcher
@en
wetenschapper
@nl
name
Vladimir Varlen Bamm
@en
Vladimir Varlen Bamm
@nl
type
label
Vladimir Varlen Bamm
@en
Vladimir Varlen Bamm
@nl
prefLabel
Vladimir Varlen Bamm
@en
Vladimir Varlen Bamm
@nl
P106
P31
P496
0000-0002-3686-1991