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De novo design of pH-responsive self-assembling helical protein filaments

Biology

De novo design of pH-responsive self-assembling helical protein filaments

H. Shen, E. M. Lynch, et al.

Discover the groundbreaking work of Hao Shen, Eric M. Lynch, and their colleagues as they unveil the design of pH-responsive protein filaments. These innovative subunits can swiftly transform between assembled and disassembled states in response to pH changes, paving the way for responsive nanomaterials with numerous applications.

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~3 min • Beginner • English
Abstract
Biological evolution has led to precise and dynamic nanostructures that reconfigure in response to pH and other environmental conditions. However, designing micrometre-scale protein nanostructures that are environmentally responsive remains a challenge. Here we describe the de novo design of pH-responsive protein filaments built from subunits containing six or nine buried histidine residues that assemble into micrometre-scale, well-ordered fibres at neutral pH. The cryogenic electron microscopy structure of an optimized design is nearly identical to the computational design model for both the subunit internal geometry and the subunit packing into the fibre. Electron, fluorescent and atomic force microscopy characterization reveal a sharp and reversible transition from assembled to disassembled fibres over 0.3 pH units, and rapid fibre disassembly in less than 1 s following a drop in pH. The midpoint of the transition can be tuned by modulating buried histidine-containing hydrogen bond networks. Computational protein design thus provides a route to creating unbound nanomaterials that rapidly respond to small pH changes.
Publisher
Nature Nanotechnology
Published On
Jul 01, 2024
Authors
Hao Shen, Eric M. Lynch, Susrut Akkineni, Joseph L. Watson, Justin Decarreau, Neville P. Bethel, Issa Benna, William Sheffler, Daniel Farrell, Frank DiMaio, Emmanuel Derivery, James J. De Yoreo, Justin Kollman, David Baker
Tags
pH-responsive
protein filaments
nanomaterials
computational design
histidine residues
micrometre-scale fibres
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