The theory of frame ordering: observing motions in calmodulin complexes. (2019)

• Record Type: Journal Article
• Authors: d'Auvergne, Edward James; Griesinger, Christian
• Is Part Of: Quarterly reviews of biophysics. Volume 52(2019)
• Publication Date: 2019
• Subjects: Biophysics, -- calmodulin, -- frame order, -- molecular dynamics, -- statistical mechanics; Biophysics -- Periodicals; 571.405
• DOI: 10.1017/S0033583519000015
• Languages: English
• ISSNs: 0033-5835

Abstract

Abstract: Large scale functional motions of molecules are studied experimentally using numerous molecular and biophysics techniques, the data from which are subsequently interpreted using diverse models of Brownian molecular dynamics. To unify all rotational physics techniques and motional models, the frame order tensor – a universal statistical mechanics theory based on the rotational ordering of rigid body frames – is herein formulated. The frame ordering is the fundamental physics that governs how motions modulate rotational molecular physics and it defines the properties and maximum information content encoded in the observable physics. Using the tensor to link residual dipolar couplings and pseudo-contact shifts, two distinct information-rich and atomic-level biophysical measurements from the field of nuclear magnetic resonance spectroscopy, to a number of basic mechanical joint models, a highly dynamic state of calmodulin (CaM) bound to a target peptide in a tightly closed conformation was observed. Intra- and inter-domain motions reveal the CaM complex to be entropically primed for peptide release.