Travelling-wave ion mobility mass spectrometry elucidates structures of gold fingers
"The zinc ions in zinc fingers bind to four sulfur or nitrogen atoms of the protein's cysteine and histidine residues," explains Nicholas P. Farrell of Virginia Commonwealth University (Richmond, USA). "Gold ions bind to just two amino acid fragments and change the conformation of the protein. The "gold fingers" are no longer able to bind to nucleic acids, which may be therapeutically useful." Although there are a variety of potential binding sites for metal ions, each metalloprotein usually prefers a single conformation. It was previously not possible to determine where the specific binding sites were in a mixture of conformers. Farrell and his team have now closely examined two gold fingers. According to Farrell, "replacing the zinc in zinc finger 3 of Sp1 transcription factor leads to only a single gold finger species." The researchers identified this as having a linear Cys-Au-His bond. In the case of the HIV nucleocapsid protein, whi...