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Updated: Mar 23, 2026

Study of Protein Dynamics via Neutron Spin Echo Spectroscopy
Published on: April 13, 2022
Fast antibody fragment motion: flexible linkers act as entropic spring
Laura R Stingaciu1, Oxana Ivanova2, Michael Ohl1
1Jülich Centre for Neutron Science JCNS, Forschungszentrum Jülich GmbH, outstation at SNS, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.
Abstract:
A flexible linker region between three fragments allows antibodies to adjust their binding sites to an antigen or receptor. Using Neutron Spin Echo Spectroscopy we observed fragment motion on a timescale of 7 ns with motional amplitudes of about 1 nm relative to each other. The mechanistic complexity of the linker region can be described by a spring model with Brownian motion of the fragments in a harmonic potential. Displacements, timescale, friction and force constant of the underlying dynamics are accessed. The force constant exhibits a similar strength to an entropic spring, with friction of the fragment matching the unbound state. The observed fast motions are fluctuations in pre-existing equilibrium configurations. The Brownian motion of domains in a harmonic potential is the appropriate model to examine functional hinge motions dependent on the structural topology and highlights the role of internal forces and friction to function.
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