Gd3 + Spin Labeling for Measuring Distances in Biomacromolecules
dc.contributor.author | Feintuch, Akiva | en |
dc.contributor.author | Otting, Gottfried | en |
dc.contributor.author | Goldfarb, Daniella | en |
dc.date.accessioned | 2025-05-27T21:20:32Z | |
dc.date.available | 2025-05-27T21:20:32Z | |
dc.date.issued | 2015 | en |
dc.description.abstract | Applications of distance measurements by pulse dipolar electron-paramagnetic resonance (PD-EPR) spectroscopy to structural biology are based on introducing spin labels (SLs) at well-defined locations in the biomacromolecule. The most commonly used SLs are nitroxyl radicals, but recently SLs based on high-spin Gd3 + (S = 7/2) complexes have been shown to be an attractive alternative for PD-EPR, particularly double electron-electron resonance (DEER), at spectrometer frequencies higher than 30 GHz. In this chapter, we describe the advantage of using this new family of SLs in terms of sensitivity, stability, and chemical diversity. We present current labeling strategies for proteins, discuss the approximations under which DEER data analysis of a pair of Gd3 + SLs (GdSLs) is equivalent to that of a pair of S = 1/2 SLs, and discuss the reduction in multispin effects in a cluster of GdSLs, as opposed to a cluster of nitroxide labels, which can be found in oligomeric systems. In addition, we provide a brief overview of the current, rather limited, knowledge of Gd3 + phase relaxation behavior and describe experimental strategies in terms of optimizing sensitivity. The possibility of using several types of SLs in a system allows one to isolate effects due to the chemical nature of the SL itself; several such examples are presented, focusing on comparing nitroxide and GdSLs. Finally, we will discuss the initial results on in-cell DEER with GdSLs. | en |
dc.description.sponsorship | Financial support by the ISF (Israel Science Foundation), the BSF (USA-Israel bi-national science foundation), the Australian Research Council, and an Australia-Weizmann Making Connections grant are gratefully acknowledged. In part, this research was made possible by the historic generosity of the Harold Perlman family. D.G. holds the Erich Klieger Professorial Chair in Chemical Physics. | en |
dc.description.status | Peer-reviewed | en |
dc.format.extent | 43 | en |
dc.identifier.issn | 0076-6879 | en |
dc.identifier.other | Scopus:84944355772 | en |
dc.identifier.other | PubMed:26478494 | en |
dc.identifier.other | ARIES:U3488905xPUB5818 | en |
dc.identifier.uri | http://www.scopus.com/inward/record.url?scp=84944355772&partnerID=8YFLogxK | en |
dc.identifier.uri | https://dspace-test.anu.edu.au/handle/1885/733758774 | |
dc.language.iso | en | en |
dc.publisher | Academic Press Inc. | en |
dc.relation.ispartofseries | Methods in Enzymology | en |
dc.rights | Publisher Copyright: © 2015 Elsevier Inc. | en |
dc.subject | DEER | en |
dc.subject | Distance measurements | en |
dc.subject | EPR spectroscopy | en |
dc.subject | Gd tags | en |
dc.subject | High-field EPR | en |
dc.subject | Spin labels | en |
dc.title | Gd3 + Spin Labeling for Measuring Distances in Biomacromolecules | en |
dc.type | Book chapter | en |
local.bibliographicCitation.lastpage | 457 | en |
local.bibliographicCitation.startpage | 415 | en |
local.contributor.affiliation | Feintuch, Akiva; Weizmann Institute of Science | en |
local.contributor.affiliation | Otting, Gottfried; Wearable and Portable Devices, Research School of Chemistry, ANU College of Science and Medicine, The Australian National University | en |
local.contributor.affiliation | Goldfarb, Daniella; Weizmann Institute of Science | en |
local.identifier.doi | 10.1016/bs.mie.2015.07.006 | en |
local.identifier.essn | 1557-7988 | en |
local.identifier.pure | 2164a90a-dad5-4fac-9479-83cd3a42971a | en |
local.type.status | Published | en |