Metamorphic Proteins to Achieve Conformationally Selective Material Surface Binding

The controlled binding of proteins on nanoparticle surfaces remains a grand challenge required for many applications ranging from biomedical to energy storage. The difficulty in achieving this ability arises from the different functional groups of the biomolecule that can adsorb on the nanoparticle surface. While most proteins can only adopt a single structure, metamorphic proteins can access at least two different conformations, which presents intriguing opportunities to exploit such structural variations for binding to nanoparticles. Such effects are examined using calmodulin, a sensing messenger protein, that can adopt two conformations based on Ca<sup>2+</sup> binding. The affinity of the apo and holo forms of the protein for Au is examined using a highly integrated set of experimental and computation studies, which demonstrated significantly enhanced binding for the holo protein as compared to the apo. Such effects are proposed to arise from changes in the protein structure, which lead to substantially varied biomolecular surfaces that facilitate both Au adsorption and protein-protein assembly once adsorbed. Such studies provide critical information for protein structural design to control nanoparticle adsorption for wide-ranging applications.

Authors

Institutions

Publication Details

Journal
Small
Published
2025-01-10
DOI
https://doi.org/10.1002/smll.202408141
Primary Topic
Molecular Junctions and Nanostructures
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Metamorphic Proteins to Achieve Conformationally Selective Material Surface Binding

Dominic J. Glover, Lorenzo Travaglini, S. Ramamurthy, Artur Sawicki et al.
Small
Molecular Junctions and Nanostructures
article

Metamorphic Proteins to Achieve Conformationally Selective Material Surface Binding

Dominic J. Glover, Lorenzo Travaglini, S. Ramamurthy, Artur Sawicki, Tiffany R. Walsh, Hassan Monhemi, Marc R. Knecht, Patrick B. Dennis, Kyle B. Meerbott, Joseph M. Slocik
article en

Abstract

The controlled binding of proteins on nanoparticle surfaces remains a grand challenge required for many applications ranging from biomedical to energy storage. The difficulty in achieving this ability arises from the different functional groups of the biomolecule that can adsorb on the nanoparticle surface. While most proteins can only adopt a single structure, metamorphic proteins can access at least two different conformations, which presents intriguing opportunities to exploit such structural variations for binding to nanoparticles. Such effects are examined using calmodulin, a sensing messenger protein, that can adopt two conformations based on Ca<sup>2+</sup> binding. The affinity of the apo and holo forms of the protein for Au is examined using a highly integrated set of experimental and computation studies, which demonstrated significantly enhanced binding for the holo protein as compared to the apo. Such effects are proposed to arise from changes in the protein structure, which lead to substantially varied biomolecular surfaces that facilitate both Au adsorption and protein-protein assembly once adsorbed. Such studies provide critical information for protein structural design to control nanoparticle adsorption for wide-ranging applications.

SmallVol. 21(7)
United States Air Force Research Laboratory (US), University of Miami (US), Deakin University (AU), UNSW Sydney (AU), Dr. John T. Macdonald Foundation (US)
Australian National Fabrication Facility, National Computational Infrastructure, University of New South Wales, National Cancer Institute, Army Research Office
Affordable and clean energy
Openalex Percentile: Top 100%
Molecular Junctions and Nanostructures
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.