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A thoughtful consideration of the implications of protein breathing for antibody-mediated virus neutralization in the context of flaviviruses

Overview It has long been known that one way to obtain a pool of bioavailable Fe II required for protein metalation in bacterial cells is to store it in intracellular compartments, notably heme-based bacterioferritins, ferritins, or in mini-ferritins, derived from the superfamily of DNA-binding proteins from starved cells (Dps), all of which are protein-coated biomineralized compartments of Fe II and Fe III

Yes, ultraviolet and fluorescent light cause oxidative damage to methionine and tryptophan residues in IGF-1 LR3, which compromises receptor binding affinity even in lyophilised form

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Supports tissue regeneration*