The pH-dependent structures of the ferritin shell (apoferritin, 24-mer) and the ferrihydrite core, under physiological conditions that permit enzymatic activity, were investigated by synchrotron small-angle X-ray scattering (SAXS). The solution structure of apoferritin was found to be nearly identical to the crystal structure. The shell thickness and hollow core volumes were estimated. The intact hollow spherical apoferritin was stable over a wide pH range, 3.40-10.0, and the ferrihydrite core was stable over the pH range 2.10-10.0. The apoferritin subunits underwent aggregation below pH 0.80, whereas the ferrihydrite cores aggregated below pH 2.10 as a result of the disassembly of the ferritin shell under the strongly acidic conditions. As...
Ferritin proteins function to detoxify, solubilize and store cellular iron by directing the synthesi...
The structure and dynamics of the spherical protein Apoferritin in aqueous solution are studied over...
Physico-chemical characterization of biomacromolecule magnet of erritin in terms of morphology, stru...
Ferritin, a protein that is present in the human body for a controlled iron storage and release, con...
The structural stability of magnetoferritin, a synthetic analogue of ferritin, at various pH levels ...
Native, undried, crystalline apoferritin, prepared from ferritin, was studied in aqueous solution (0...
Apoferritin is a complex protein potential for drug delivery application. The advantage of apoferrit...
DoctorMolecular structure and property of various biomacromolecules were investigated by solution X-...
Ferritins are a family of proteins distributed widely in nature. In bacterial, plant, and animal cel...
THE structure of ferritin is of considerable interest because of its widespread occurrence in higher...
Synthetic biological macromolecule of magnetoferritin containing an iron oxide core inside a protein...
Ferritin is found in various mammalian tissues as well as in lower organisms and in plants. It store...
The denaturation of recombinant horse L-chain apoferritin (rLF), which is composed of 24 L-chain sub...
The assembly reaction of <i>Escherichia coli</i> ferritin A (EcFtnA) was studied using time-resolved...
Various proteins form nanostructures exhibiting unique functions, making them attractive as next-gen...
Ferritin proteins function to detoxify, solubilize and store cellular iron by directing the synthesi...
The structure and dynamics of the spherical protein Apoferritin in aqueous solution are studied over...
Physico-chemical characterization of biomacromolecule magnet of erritin in terms of morphology, stru...
Ferritin, a protein that is present in the human body for a controlled iron storage and release, con...
The structural stability of magnetoferritin, a synthetic analogue of ferritin, at various pH levels ...
Native, undried, crystalline apoferritin, prepared from ferritin, was studied in aqueous solution (0...
Apoferritin is a complex protein potential for drug delivery application. The advantage of apoferrit...
DoctorMolecular structure and property of various biomacromolecules were investigated by solution X-...
Ferritins are a family of proteins distributed widely in nature. In bacterial, plant, and animal cel...
THE structure of ferritin is of considerable interest because of its widespread occurrence in higher...
Synthetic biological macromolecule of magnetoferritin containing an iron oxide core inside a protein...
Ferritin is found in various mammalian tissues as well as in lower organisms and in plants. It store...
The denaturation of recombinant horse L-chain apoferritin (rLF), which is composed of 24 L-chain sub...
The assembly reaction of <i>Escherichia coli</i> ferritin A (EcFtnA) was studied using time-resolved...
Various proteins form nanostructures exhibiting unique functions, making them attractive as next-gen...
Ferritin proteins function to detoxify, solubilize and store cellular iron by directing the synthesi...
The structure and dynamics of the spherical protein Apoferritin in aqueous solution are studied over...
Physico-chemical characterization of biomacromolecule magnet of erritin in terms of morphology, stru...