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Blahut, J.* ; Brandl, M.J.* ; Sarkar, R. ; Reif, B. ; Tošner, Z.*

Optimal control derived sensitivity-enhanced CA-CO mixing sequences for MAS solid-state NMR – Applications in sequential protein backbone assignments.

J. Magn. Reson. Open 16-17:100122 (2023)
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We have recently introduced optimal-control derived pulse sequences for sensitivity-enhanced heteronuclear correlation NMR experiments of solid proteins. Preservation of equivalent coherence transfer pathways using transverse-mixing pulses (TROP) in multidimensional pulse schemes allows to increase the sensitivity of the experiments by more than a factor of 2 per each indirect dimension. In this article, we present homonuclear CA-CO transverse-mixing elements (homoTROP) that are based on dipolar interactions and achieve similar gains as the heteronuclear TROP pulses described previously. Both transfer elements were subsequently implemented in 3D se-hCAcoNH and se-hCOcaNH, that together with the previously introduced 3D se-hCANH and se-hCONH experiments yield a complete set of sensitivity-enhanced protein backbone assignment experiments. In contrast to the J-coupling based methods that are used at fast (60 kHz) and ultrafast MAS (>100 kHz), the homoTROP experiments employ about 10-times shorter mixing times making use of the larger magnitude of the dipolar coupling in comparison to the J couplings. The experiments are demonstrated using a microcrystalline, perdeuterated sample of the chicken alpha-spectrin SH3 domain in which all exchangeable sites are fully back-substituted with protons. We evaluated the gains in efficiency in all experiments site-specifically observing that the se-hCAcoNH and se-hCOcaNH experiments yield an increase in sensitivity by a factor of 1.36±0.09 and at least a factor of 1.8 with respect to the conventional hcoCAcoNH and hCOcaNH J-based experiments.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Fully Protonated Proteins; Cross-polarization; Spectroscopy; Resonance; Dynamics; Simulation; Nco
Language english
Publication Year 2023
HGF-reported in Year 2023
ISSN (print) / ISBN 2666-4410
e-ISSN 2666-4410
Quellenangaben Volume: 16-17, Issue: , Pages: , Article Number: 100122 Supplement: ,
Publisher Elsevier
Publishing Place Radarweg 29, 1043 Nx Amsterdam, Netherlands
Reviewing status Peer reviewed
POF-Topic(s) 30203 - Molecular Targets and Therapies
Research field(s) Enabling and Novel Technologies
PSP Element(s) G-503090-001
Grants European Regional Development Fund-Project "UP CIISB"
CF NMR of CIISB, Instruct -CZ center
MEYS CR
Czech Science Foundation
German Research Foundation
Scopus ID 85164037970
Erfassungsdatum 2023-10-18