Abstract

Bioinorganic chemists aspire to achieve the same exquisite and highly controlled inorganic chemistry featured in biology. An exciting mimetic approach involves the use of miniature artificial protein scaffolds designed de novo (often based on the coiled coil (CC) scaffold), for reproducing native metal ion sites and their function. Recently, there is increased interest, instead, in the design of xeno-metal sites within CC assemblies. This involves incorporating either non-biological metal ions, cofactors or non-proteinogenic amino acid ligands for metal ion coordination, whilst retaining a minimal CC protein scaffold. Using this approach, one should be able to create functional designs with unique and unusual properties, which combine the advantages of both biology and 'traditional' non-biological inorganic chemistry. It is the recent progress with respect to the design of xeno-metallo CCs which will be discussed in this Focus Review.

Highlights

  • Xeno-metalsMetal ions are essential for many biological processes, Nature selects from a rather limited range

  • It has been estimated that roughly a third of all native proteins contain metal ions which are essential for their function,[1] making the study of metalloproteins an attractive and worthwhile goal

  • The ability to artificially replicate challenging metal ion sites, both structurally and functionally, as well as recreating the exquisite bioselectivity and control displayed in biology, is one of the principle challenges of bioinorganic chemistry

Read more

Summary

Xeno-metals

Metal ions are essential for many biological processes, Nature selects from a rather limited range. Contrast this with the inorganic chemists’ toolbox, which has the breadth of elements across the Periodic Table to choose from, and the potential to develop systems with a much more diverse range of properties and potential applications. This section focuses on some key examples where xeno binding sites, inspired by nonbiological Inorganic Chemistry, have been engineered into a CC scaffold

Lanthanides
Rhodium
Ruthenium
Metallo-porphyrins
Non-proteinogenic amino acids
Heterocyclic derivatives
Penicillamine and D-amino acids – modification of steric bulk
Conclusions and perspectives
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call