Structural dynamics of the chromo-shadow domain and chromodomain of HP1 bound to histone H3K9 methylated peptide, as measured by site-directed spin-labeling EPR spectroscopy

2021 ◽  
Vol 567 ◽  
pp. 42-48
Author(s):  
Isao Suetake ◽  
Shigeaki Nakazawa ◽  
Kazunobu Sato ◽  
Risa Mutoh ◽  
Yuichi Mishima ◽  
...  
2021 ◽  
Vol 120 (3) ◽  
pp. 293a
Author(s):  
William D. Carbo ◽  
Matthew Scheyer ◽  
Alberto Perez ◽  
Samuel Haralu ◽  
Gary A. Lorigan ◽  
...  

2020 ◽  
Vol 11 (35) ◽  
pp. 9655-9664
Author(s):  
Yan Wang ◽  
Venkatesan Kathiresan ◽  
Yaoyi Chen ◽  
Yanping Hu ◽  
Wei Jiang ◽  
...  

Site-directed spin labeling (SDSL) of large RNAs for electron paramagnetic resonance (EPR) spectroscopy has remained challenging to date.


2007 ◽  
Vol 37 (4) ◽  
pp. 483-493 ◽  
Author(s):  
Marcin Sarewicz ◽  
Sebastian Szytuła ◽  
Małgorzata Dutka ◽  
Artur Osyczka ◽  
Wojciech Froncisz

2013 ◽  
Vol 394 (10) ◽  
pp. 1281-1300 ◽  
Author(s):  
Johann P. Klare

Abstract Site-directed spin labeling (SDSL) in combination with electron paramagnetic resonance (EPR) spectroscopy has emerged as an efficient tool to elucidate the structure and the conformational dynamics of proteins under conditions close to the native state. This review article summarizes the basics as well as the recent progress in SDSL and EPR methods, especially for investigations on protein structure, protein function, and interaction of proteins with other proteins or nucleic acids. Labeling techniques as well as EPR methods are introduced and exemplified with applications to systems that have been studied in the author’s laboratory in the past 15 years, headmost the sensory rhodopsin-transducer complex mediating the photophobic response of the halophilic archaeum Natronomonas pharaonis. Further examples underline the application of SDSL EPR spectroscopy to answer specific questions about the system under investigation, such as the nature and influence of interactions of proteins with other proteins or nucleic acids. Finally, it is discussed how SDSL EPR can be combined with other biophysical techniques to combine the strengths of the different methodologies.


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