J
Jack H. Freed
Researcher at Cornell University
Publications - 468
Citations - 24789
Jack H. Freed is an academic researcher from Cornell University. The author has contributed to research in topics: Electron paramagnetic resonance & Relaxation (NMR). The author has an hindex of 82, co-authored 459 publications receiving 23392 citations. Previous affiliations of Jack H. Freed include Dartmouth College & University of Freiburg.
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Journal ArticleDOI
An Assessment of the Applicability of Multifrequency ESR to Study the Complex Dynamics of Biomolecules
Zhichun Liang,Jack H. Freed +1 more
TL;DR: In this article, it was shown that the commonly used models for analyzing ESR spectra from spin-labeled proteins or DNA systems are special cases of the more general slowly relaxing local structure (SRLS) model, wherein the nitroxide spin probe is taken as reorienting in a restricted local environment, which itself is relaxing on a longer time scale.
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Solvent Effects in Electron Spin Resonance Spectra
TL;DR: In this paper, it was shown that the changes in splittings arise entirely from a redistribution of the pi-electron spin density, and that the spin density is affected only by localized complexes between the solvent and polar substituents or heteroatoms in the radical.
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Anisotropic Rotational Diffusion and Electron Spin Resonance Linewidths
TL;DR: In this paper, the authors extended the theory of ESR linewidths for dilute solutions of free radicals developed by Freed and Fraenkel to cover the possibility that the rotational motions of the free radicals are anisotropic.
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Maximum entropy: A complement to Tikhonov regularization for determination of pair distance distributions by pulsed ESR
TL;DR: The maximum entropy regularization method (MEM) is regarded as a complement to TikR by securing a positive pair distance distribution and enhancing the accuracy of TIKR.
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Transport domain unlocking sets the uptake rate of an aspartate transporter
Nurunisa Akyuz,Elka R. Georgieva,Zhou Zhou,Sebastian Stolzenberg,Michel A. Cuendet,George Khelashvili,Roger B. Altman,Daniel S. Terry,Jack H. Freed,Harel Weinstein,Olga Boudker,Scott C. Blanchard +11 more
TL;DR: It is shown that GltPh bearing two mutations introduced to impart characteristics of the human transporter exhibits markedly increased transport domain dynamics, which parallels an increased rate of substrate transport, thereby establishing a direct temporal relationship between transport domain motion and substrate uptake.