Literature DB >> 20022272

Group epitope mapping considering relaxation of the ligand (GEM-CRL): including longitudinal relaxation rates in the analysis of saturation transfer difference (STD) experiments.

Sebastian Kemper1, Mitul K Patel, James C Errey, Benjamin G Davis, Jonathan A Jones, Timothy D W Claridge.   

Abstract

In the application of saturation transfer difference (STD) experiments to the study of protein-ligand interactions, the relaxation of the ligand is one of the major influences on the experimentally observed STD factors, making interpretation of these difficult when attempting to define a group epitope map (GEM). In this paper, we describe a simplification of the relaxation matrix that may be applied under specified experimental conditions, which results in a simplified equation reflecting the directly transferred magnetisation rate from the protein onto the ligand, defined as the summation over the whole protein of the protein-ligand cross-relaxation multiplied by with the fractional saturation of the protein protons. In this, the relaxation of the ligand is accounted for implicitly by inclusion of the experimentally determined longitudinal relaxation rates. The conditions under which this "group epitope mapping considering relaxation of the ligand" (GEM-CRL) can be applied were tested on a theoretical model system, which demonstrated only minor deviations from that predicted by the full relaxation matrix calculations (CORCEMA-ST) [7]. Furthermore, CORCEMA-ST calculations of two protein-saccharide complexes (Jacalin and TreR) with known crystal structures were performed and compared with experimental GEM-CRL data. It could be shown that the GEM-CRL methodology is superior to the classical group epitope mapping approach currently used for defining ligand-protein proximities. GEM-CRL is also useful for the interpretation of CORCEMA-ST results, because the transferred magnetisation rate provides an additional parameter for the comparison between measured and calculated values. The independence of this parameter from the above mentioned factors can thereby enhance the value of CORCEMA-ST calculations. Copyright (c) 2009 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 20022272     DOI: 10.1016/j.jmr.2009.11.015

Source DB:  PubMed          Journal:  J Magn Reson        ISSN: 1090-7807            Impact factor:   2.229


  11 in total

1.  Evaluation of ligand-based NMR screening methods to characterize small molecule binding to HIV-1 glycoprotein-41.

Authors:  Shidong Chu; Guangyan Zhou; Miriam Gochin
Journal:  Org Biomol Chem       Date:  2017-06-07       Impact factor: 3.876

2.  Detecting and Characterizing Interactions of Metabolites with Proteins by Saturation Transfer Difference Nuclear Magnetic Resonance (STD NMR) Spectroscopy.

Authors:  Ruslan Nedielkov; Heiko M Möller
Journal:  Methods Mol Biol       Date:  2023

3.  Probing the Functional Interaction Interface of Lipopolysaccharide and Antimicrobial Peptides: A Solution-State NMR Perspective.

Authors:  Karishma Biswas; Anirban Bhunia
Journal:  Methods Mol Biol       Date:  2022

4.  Development of inhibitors of heterotrimeric Gαi subunits.

Authors:  Kathryn M Appleton; Kevin J Bigham; Christopher C Lindsey; Starr Hazard; Jonel Lirjoni; Stuart Parnham; Mirko Hennig; Yuri K Peterson
Journal:  Bioorg Med Chem       Date:  2014-04-26       Impact factor: 3.641

5.  Solution structure of a bacterial microcompartment targeting peptide and its application in the construction of an ethanol bioreactor.

Authors:  Andrew D Lawrence; Stefanie Frank; Sarah Newnham; Matthew J Lee; Ian R Brown; Wei-Feng Xue; Michelle L Rowe; Daniel P Mulvihill; Michael B Prentice; Mark J Howard; Martin J Warren
Journal:  ACS Synth Biol       Date:  2014-02-24       Impact factor: 5.110

6.  Conformational Changes in Tyrosine 11 of Neurotensin Are Required to Activate the Neurotensin Receptor 1.

Authors:  Fabian Bumbak; Trayder Thomas; Billy J Noonan-Williams; Tasneem M Vaid; Fei Yan; Alice R Whitehead; Shoni Bruell; Martina Kocan; Xuan Tan; Margaret A Johnson; Ross A D Bathgate; David K Chalmers; Paul R Gooley; Daniel J Scott
Journal:  ACS Pharmacol Transl Sci       Date:  2020-04-29

7.  Optimising selective excitation pulses to maximise saturation transfer difference NMR spectroscopy.

Authors:  Nathan B Ley; Michelle L Rowe; Richard A Williamson; Mark J Howard
Journal:  RSC Adv       Date:  2014-01-08       Impact factor: 3.361

8.  Q2DSTD NMR deciphers epitope-mapping variability for peptide recognition of integrin αvβ6.

Authors:  Jessica L Sorge; Jane L Wagstaff; Michelle L Rowe; Richard A Williamson; Mark J Howard
Journal:  Org Biomol Chem       Date:  2015-06-29       Impact factor: 3.876

9.  The role of 2,4-dihydroxyquinoline (DHQ) in Pseudomonas aeruginosa pathogenicity.

Authors:  Jordon D Gruber; Wei Chen; Stuart Parnham; Kevin Beauchesne; Peter Moeller; Patrick A Flume; Yong-Mei Zhang
Journal:  PeerJ       Date:  2016-01-07       Impact factor: 2.984

10.  Fluorinated Carbohydrates as Lectin Ligands: (19)F-Based Direct STD Monitoring for Detection of Anomeric Selectivity.

Authors:  João P Ribeiro; Tammo Diercks; Jesús Jiménez-Barbero; Sabine André; Hans-Joachim Gabius; Francisco Javier Cañada
Journal:  Biomolecules       Date:  2015-11-13
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.