Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils

Herein, we establish for the first time the design principles for lanthanide coordination within coiled coils, and the important consequences of binding site translation. By interrogating design requirements and by systematically translating binding site residues, one can influence coiled coil stabi...

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Main Authors: Berwick, Matthew R., Slope, Louise N., Smith, Caitlin F., King, Siobhan M., Newton, Sarah L., Gillis, Richard B., Adams, Gary G., Rowe, Arthur J., Harding, Stephen E., Britton, Melanie M., Peacock, Anna F. A.
Format: Article
Published: Royal Society of Chemistry 2015
Online Access:https://eprints.nottingham.ac.uk/41718/
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author Berwick, Matthew R.
Slope, Louise N.
Smith, Caitlin F.
King, Siobhan M.
Newton, Sarah L.
Gillis, Richard B.
Adams, Gary G.
Rowe, Arthur J.
Harding, Stephen E.
Britton, Melanie M.
Peacock, Anna F. A.
author_facet Berwick, Matthew R.
Slope, Louise N.
Smith, Caitlin F.
King, Siobhan M.
Newton, Sarah L.
Gillis, Richard B.
Adams, Gary G.
Rowe, Arthur J.
Harding, Stephen E.
Britton, Melanie M.
Peacock, Anna F. A.
author_sort Berwick, Matthew R.
building Nottingham Research Data Repository
collection Online Access
description Herein, we establish for the first time the design principles for lanthanide coordination within coiled coils, and the important consequences of binding site translation. By interrogating design requirements and by systematically translating binding site residues, one can influence coiled coil stability and more importantly, the lanthanide coordination chemistry. A 10 °A binding site translation along a coiled coil, transforms a coordinatively saturated Tb(Asp) ₃(Asn) ₃ site into one in which three exogenous water molecules are coordinated, and in which the Asn layer is no longer essential for binding, Tb(Asp)₃(H₂O ) ₃. This has a profound impact on the relaxivity of the analogous Gd(III) coiled coil, with more than a fourfold increase in the transverse relaxivity (21 to 89 mM⁻¹ s⁻¹), by bringing into play, in addition to the outer sphere mechanism present for all Gd(III) coiled coils, an inner sphere mechanism. Not only do these findings warrant further investigation for possible exploitation as MRI contrast agents, but understanding the impact of binding site translation on coordination chemistry has important repercussions for metal binding site design, taking us an important step closer to the predictable and truly de novo design of metal binding sites, for new functional applications.
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spelling nottingham-417182020-05-04T17:25:56Z https://eprints.nottingham.ac.uk/41718/ Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils Berwick, Matthew R. Slope, Louise N. Smith, Caitlin F. King, Siobhan M. Newton, Sarah L. Gillis, Richard B. Adams, Gary G. Rowe, Arthur J. Harding, Stephen E. Britton, Melanie M. Peacock, Anna F. A. Herein, we establish for the first time the design principles for lanthanide coordination within coiled coils, and the important consequences of binding site translation. By interrogating design requirements and by systematically translating binding site residues, one can influence coiled coil stability and more importantly, the lanthanide coordination chemistry. A 10 °A binding site translation along a coiled coil, transforms a coordinatively saturated Tb(Asp) ₃(Asn) ₃ site into one in which three exogenous water molecules are coordinated, and in which the Asn layer is no longer essential for binding, Tb(Asp)₃(H₂O ) ₃. This has a profound impact on the relaxivity of the analogous Gd(III) coiled coil, with more than a fourfold increase in the transverse relaxivity (21 to 89 mM⁻¹ s⁻¹), by bringing into play, in addition to the outer sphere mechanism present for all Gd(III) coiled coils, an inner sphere mechanism. Not only do these findings warrant further investigation for possible exploitation as MRI contrast agents, but understanding the impact of binding site translation on coordination chemistry has important repercussions for metal binding site design, taking us an important step closer to the predictable and truly de novo design of metal binding sites, for new functional applications. Royal Society of Chemistry 2015-12-22 Article PeerReviewed Berwick, Matthew R., Slope, Louise N., Smith, Caitlin F., King, Siobhan M., Newton, Sarah L., Gillis, Richard B., Adams, Gary G., Rowe, Arthur J., Harding, Stephen E., Britton, Melanie M. and Peacock, Anna F. A. (2015) Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils. Chemical Science, 7 (3). pp. 2207-2216. ISSN 2041-6539 http://pubs.rsc.org/en/Content/ArticleLanding/2016/SC/C5SC04101E#!divAbstract doi:10.1039/c5sc04101e doi:10.1039/c5sc04101e
spellingShingle Berwick, Matthew R.
Slope, Louise N.
Smith, Caitlin F.
King, Siobhan M.
Newton, Sarah L.
Gillis, Richard B.
Adams, Gary G.
Rowe, Arthur J.
Harding, Stephen E.
Britton, Melanie M.
Peacock, Anna F. A.
Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils
title Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils
title_full Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils
title_fullStr Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils
title_full_unstemmed Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils
title_short Location dependent coordination chemistry and MRI relaxivity, in de novo designed lanthanide coiled coils
title_sort location dependent coordination chemistry and mri relaxivity, in de novo designed lanthanide coiled coils
url https://eprints.nottingham.ac.uk/41718/
https://eprints.nottingham.ac.uk/41718/
https://eprints.nottingham.ac.uk/41718/