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      HACANCOi: a new H α-detected experiment for backbone resonance assignment of intrinsically disordered proteins

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          Abstract

          Unidirectional coherence transfer is highly efficient in intrinsically disordered proteins (IDPs). Their elevated ps-ns timescale dynamics ensures long transverse (T 2) relaxation times allowing sophisticated coherence transfer pathway selection in comparison to folded proteins. 1H α-detection ensures non-susceptibility to chemical exchange with the solvent and enables chemical shift assignment of consecutive proline residues, typically abundant in IDPs. However, many IDPs undergo a disorder-to-order transition upon interaction with their target protein, which leads to the loss of the favorable relaxation properties. Long coherence transfer routes now result in prohibitively large decrease in sensitivity. We introduce a novel 4D 1H α-detected experiment HACANCOi, together with its 3D implementation, which warrant high sensitivity for the assignment of proline-rich regions in IDPs in complex with a globular protein. The experiment correlates 1H α i, 13C α i, 15N i and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$^{13} C^{\prime}_{i}$$\end{document} spins by transferring the magnetization concomitantly from 13C α i to 15N i and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$^{13} C^{\prime}_{i}$$\end{document} . The B1 domain of protein G (GB1), and the enteropathogenic E. coli EspF in complex with human SNX9 SH3, serve as model systems to demonstrate the attainable sensitivity and successful sequential assignment.

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          The CCPN data model for NMR spectroscopy: development of a software pipeline.

          To address data management and data exchange problems in the nuclear magnetic resonance (NMR) community, the Collaborative Computing Project for the NMR community (CCPN) created a "Data Model" that describes all the different types of information needed in an NMR structural study, from molecular structure and NMR parameters to coordinates. This paper describes the development of a set of software applications that use the Data Model and its associated libraries, thus validating the approach. These applications are freely available and provide a pipeline for high-throughput analysis of NMR data. Three programs work directly with the Data Model: CcpNmr Analysis, an entirely new analysis and interactive display program, the CcpNmr FormatConverter, which allows transfer of data from programs commonly used in NMR to and from the Data Model, and the CLOUDS software for automated structure calculation and assignment (Carnegie Mellon University), which was rewritten to interact directly with the Data Model. The ARIA 2.0 software for structure calculation (Institut Pasteur) and the QUEEN program for validation of restraints (University of Nijmegen) were extended to provide conversion of their data to the Data Model. During these developments the Data Model has been thoroughly tested and used, demonstrating that applications can successfully exchange data via the Data Model. The software architecture developed by CCPN is now ready for new developments, such as integration with additional software applications and extensions of the Data Model into other areas of research.
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            Pure absorption gradient enhanced heteronuclear single quantum correlation spectroscopy with improved sensitivity

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              A general enhancement scheme in heteronuclear multidimensional NMR employing pulsed field gradients.

              General pulse sequence elements that achieve sensitivity-enhanced coherence transfer from a heteronucleus to protons of arbitrary multiplicity are introduced. The building blocks are derived from the sensitivity-enhancement scheme introduced by Cavanagh et al. ((1991) J. Magn. Reson., 91, 429-436), which was used in conjunction with gradient coherence selection by Kay et al. ((1992) J. Am. Chem. Soc., 114, 10663-10665), as well as from a multiple-pulse sequence effecting a heteronuclear planar coupling Hamiltonian. The building blocks are incorporated into heteronuclear correlation experiments, in conjunction with coherence selection by the formation of a heteronuclear gradient echo. This allows for efficient water suppression without the need for water presaturation. The methods are demonstrated in HSQC-type experiments on a sample of a decapeptide in H2O. The novel pulse sequence elements can be incorporated into multidimensional experiments.
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                Author and article information

                Contributors
                perttu.permi@jyu.fi
                Journal
                J Biomol NMR
                J Biomol NMR
                Journal of Biomolecular Nmr
                Springer Netherlands (Dordrecht )
                0925-2738
                1573-5001
                28 October 2020
                28 October 2020
                2020
                : 74
                : 12
                : 741-752
                Affiliations
                [1 ]GRID grid.9681.6, ISNI 0000 0001 1013 7965, Department of Chemistry, Nanoscience Center, , University of Jyväskylä, ; Jyväskylä, Finland
                [2 ]GRID grid.9681.6, ISNI 0000 0001 1013 7965, Department of Biological and Environmental Science, , University of Jyväskylä, ; Jyväskylä, Finland
                Author information
                http://orcid.org/0000-0003-3154-7570
                http://orcid.org/0000-0002-1609-1651
                http://orcid.org/0000-0002-6281-1138
                Article
                347
                10.1007/s10858-020-00347-5
                7701164
                33118136
                982d402b-3bfc-4f6a-809a-e5fee37e8a29
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 11 June 2020
                : 18 September 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100005877, Luonnontieteiden ja Tekniikan Tutkimuksen Toimikunta;
                Award ID: 288235
                Award Recipient :
                Funded by: University of Jyväskylä (JYU)
                Categories
                Article
                Custom metadata
                © Springer Nature B.V. 2020

                Molecular biology
                e.coli,espf,gb1,intrinsically disordered protein,idp,resonance assignment,snx9 sh3
                Molecular biology
                e.coli, espf, gb1, intrinsically disordered protein, idp, resonance assignment, snx9 sh3

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