| Literature DB >> 34664948 |
Olav Schiemann1, Caspar A Heubach1, Dinar Abdullin1, Katrin Ackermann2, Mykhailo Azarkh3, Elena G Bagryanskaya4, Malte Drescher3, Burkhard Endeward5, Jack H Freed6, Laura Galazzo7, Daniella Goldfarb8, Tobias Hett1, Laura Esteban Hofer9, Luis Fábregas Ibáñez9, Eric J Hustedt10, Svetlana Kucher7, Ilya Kuprov11, Janet Eleanor Lovett12, Andreas Meyer13, Sharon Ruthstein14, Sunil Saxena15, Stefan Stoll16, Christiane R Timmel17, Marilena Di Valentin18, Hassane S Mchaourab10, Thomas F Prisner5, Bela Ernest Bode2, Enrica Bordignon7, Marina Bennati13, Gunnar Jeschke9.
Abstract
Distance distribution information obtained by pulsed dipolar EPR spectroscopy provides an important contribution to many studies in structural biology. Increasingly, such information is used in integrative structural modeling, where it delivers unique restraints on the width of conformational ensembles. In order to ensure reliability of the structural models and of biological conclusions, we herein define quality standards for sample preparation and characterization, for measurements of distributed dipole-dipole couplings between paramagnetic labels, for conversion of the primary time-domain data into distance distributions, for interpreting these distributions, and for reporting results. These guidelines are substantiated by a multi-laboratory benchmark study and by analysis of data sets with known distance distribution ground truth. The study and the guidelines focus on proteins labeled with nitroxides and on double electron-electron resonance (DEER aka PELDOR) measurements and provide suggestions on how to proceed analogously in other cases.Entities:
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Year: 2021 PMID: 34664948 DOI: 10.1021/jacs.1c07371
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 16.383