| Literature DB >> 29873848 |
Steven K Taylor1, Timothy H Tran2, Michael Z Liu3, Paul E Harris1, Yanping Sun4, Sachin R Jambawalikar3, Liang Tong2, Milan N Stojanovic5.
Abstract
High-relaxivity protein-complexes of GdIII are being pursued as MRI contrast agents in hope that they can be used at much lower doses that would minimize toxic-side effects of GdIII release from traditional contrast agents. We construct here a new type of protein-based MRI contrast agent, a proteinaceous cage based on a stable insulin hexamer in which GdIII is captured inside a water filled cavity. The macromolecular structure and the large number of "free" GdIII coordination sites available for water binding lead to exceptionally high relaxivities per one GdIII ion. The GdIII slowly diffuses out of this cage, but this diffusion can be prevented by addition of ligands that bind to the hexamer. The ligands that trigger structural changes in the hexamer, SCN- , Cl- and phenols, modulate relaxivities through an outside-in signaling that is allosterically transduced through the protein cage. Contrast-o-phores based on protein-caged metal ions have potential to become clinical contrast agents with environmentally-sensitive properties.Entities:
Keywords: contrast agent; environmentally sensitive; gadolinium; insulin hexamer; proteins
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Year: 2018 PMID: 29873848 PMCID: PMC6347121 DOI: 10.1002/chem.201801388
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236