| Literature DB >> 27017575 |
Manoj Kumar Pandey1, Jayasubba Reddy Yarava1, Rongchun Zhang2, Ayyalusamy Ramamoorthy2, Yusuke Nishiyama3.
Abstract
Chemical shift anisotropy (CSA) tensors offer a wealth of information for structural and dynamics studies of a variety of chemical and biological systems. In particular, CSA of amide protons can provide piercing insights into hydrogen-bonding interactions that vary with the backbone conformation of a protein and dynamics. However, the narrow span of amide proton resonances makes it very difficult to measure (1)H CSAs of proteins even by using the recently proposed 2D (1)H/(1)H anisotropic/isotropic chemical shift (CSA/CS) correlation technique. Such difficulties due to overlapping proton resonances can in general be overcome by utilizing the broad span of isotropic chemical shifts of low-gamma nuclei like (15)N. In this context, we demonstrate a proton-detected 3D (15)N/(1)H/(1)H CS/CSA/CS correlation experiment at fast MAS frequency (70kHz) to measure (1)H CSA values of unresolved amide protons of N-acetyl-(15)N-l-valyl-(15)N-l-leucine (NAVL).Entities:
Keywords: (1)H CSA; (1)H detection; 3D NMR; Amide proton; Solid-state NMR; Ultrafast MAS; peptide
Year: 2016 PMID: 27017575 PMCID: PMC4903906 DOI: 10.1016/j.ssnmr.2016.03.001
Source DB: PubMed Journal: Solid State Nucl Magn Reson ISSN: 0926-2040 Impact factor: 2.293