Peculiar features in the crystal structure of the adduct formed between cis-PtI2(NH3)2 and hen egg white lysozyme

Inorg Chem. 2013 Dec 16;52(24):13827-9. doi: 10.1021/ic402611m. Epub 2013 Nov 20.

Abstract

The reactivity of cis-diamminediiodidoplatinum(II), cis-PtI2(NH3)2, the iodo analogue of cisplatin, with hen egg white lysozyme (HEWL) was investigated by electrospray ionization mass spectrometry and X-ray crystallography. Interestingly, the study compound forms a stable 1:1 protein adduct for which the crystal structure was solved at 1.99 Å resolution. In this adduct, the Pt(II) center, upon release of one ammonia ligand, selectively coordinates to the imidazole of His15. Both iodide ligands remain bound to platinum, with this being a highly peculiar and unexpected feature. Notably, two equivalent modes of Pt(II) binding are possible that differ only in the location of I atoms with respect to ND1 of His15. The structure of the adduct was compared with that of HEWL-cisplatin, previously described; differences are stressed and their important mechanistic implications discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cisplatin / analogs & derivatives
  • Cisplatin / chemistry*
  • Cisplatin / metabolism
  • Crystallography, X-Ray
  • Models, Molecular*
  • Muramidase / chemistry*
  • Muramidase / metabolism
  • Platinum* / chemistry
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Platinum
  • hen egg lysozyme
  • Muramidase
  • Cisplatin