Abstract
Human metallothionein-3 (hMT3), also named as human neuronal growth inhibitory factor (hGIF), can inhibit the outgrowth of embryonic cortical neurons in the presence of brain extracts. In order to systematically study the structure-property-reactivity-function relationship of hGIF, our laboratory designed a series of mutants and studied their structure, property, reactivity and functions by a series of chemical and biological tools including UV spectroscopy, CD spectroscopy, NMR, chemical reaction and primary neuronal culture assays. In summary, we concluded that the bioactivity of hGIF was regulated by multiple factors, including the 6CPCP9 motif, an additional threonine insert at sequence position 5, domain-domain interactions, the structure and stability of the metal-thiolate cluster and the linker. Our studies provide more and more evidences which revealed that the bioactivity of hGIF is mainly related to the essential metal release and its characteristic conformation.
Original language | English (US) |
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Pages (from-to) | 1965-1972 |
Number of pages | 8 |
Journal | Journal of Inorganic Biochemistry |
Volume | 102 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2008 |
Keywords
- Cell bioassay
- Metallothionein (MT)
- Mutation
- Neuronal growth inhibitory factor (GIF)
- Structure-function relationship
ASJC Scopus subject areas
- Biochemistry
- Inorganic Chemistry