DNP-Supported Solid-State NMR Spectroscopy of Proteins Inside Mammalian Cells

被引:57
作者
Narasimhan, Siddarth [1 ]
Scherpe, Stephan [2 ,3 ]
Paioni, Alessandra Lucini [1 ]
van der Zwan, Johan [1 ]
Folkers, Gert E. [1 ]
Ovaa, Huib [2 ,3 ]
Baldus, Marc [1 ]
机构
[1] Univ Utrecht, NMR Spect Grp, Bijvoet Ctr Biomol Res, Padualaan 8, NL-3584 CH Utrecht, Netherlands
[2] LUMC, Oncode Inst, Einthovenweg 20, NL-2333 ZC Leiden, Netherlands
[3] LUMC, Dept Cell & Chem Biol, Einthovenweg 20, NL-2333 ZC Leiden, Netherlands
基金
欧盟地平线“2020”;
关键词
dynamic nuclear polarization; in-cell NMR; protein-protein interactions; solid-state NMR; ubiquitination; DYNAMIC NUCLEAR-POLARIZATION; MEMBRANE-PROTEINS; UBIQUITIN; COMPLEX; TOOL;
D O I
10.1002/anie.201903246
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Elucidating at atomic level how proteins interact and are chemically modified in cells represents a leading frontier in structural biology. We have developed a tailored solid-state NMR spectroscopic approach that allows studying protein structure inside human cells at atomic level under high-sensitivity dynamic nuclear polarization (DNP) conditions. We demonstrate the method using ubiquitin (Ub), which is critically involved in cellular functioning. Our results pave the way for structural studies of larger proteins or protein complexes inside human cells, which have remained elusive to in-cell solution-state NMR spectroscopy due to molecular size limitations.
引用
收藏
页码:12969 / 12973
页数:5
相关论文
共 41 条
  • [1] Dynamic Nuclear Polarization Nuclear Magnetic Resonance in Human Cells Using Fluorescent Polarizing Agents
    Albert, Brice J.
    Gao, Chukun
    Sesti, Erika L.
    Saliba, Edward P.
    Alaniva, Nicholas
    Scott, Faith J.
    Sigurdsson, Snorri Th
    Barnes, Alexander B.
    [J]. BIOCHEMISTRY, 2018, 57 (31) : 4741 - 4746
  • [2] [Anonymous], 2011, Angew. Chem, DOI DOI 10.1002/ANGE.201100886
  • [3] Combined 1H-DetectedSolid-StateNMRSpectroscopy and Electron Cryotomography to Study Membrane Proteins across Resolutions in Native Environments
    Baker, Lindsay A.
    Sinnige, Tessa
    Schellenberger, Pascale
    de Keyzer, Jeanine
    Siebert, C. Alistair
    Driessen, Arnold J. M.
    Baldus, Marc
    Grunewald, Kay
    [J]. STRUCTURE, 2018, 26 (01) : 161 - +
  • [4] A dynamic ubiquitin equilibrium couples proteasomal activity to chromatin remodeling
    Dantuma, NP
    Groothuis, TAM
    Salomons, FA
    Neefjes, J
    [J]. JOURNAL OF CELL BIOLOGY, 2006, 173 (01) : 19 - 26
  • [5] El Oualid F., 2010, Angewandte Chemie, V122, P10347
  • [6] Chemical Synthesis of Ubiquitin, Ubiquitin-Based Probes, and Diubiquitin
    El Oualid, Farid
    Merkx, Remco
    Ekkebus, Reggy
    Hameed, Dharjath S.
    Smit, Judith J.
    de Jong, Annemieke
    Hilkmann, Henk
    Sixma, Titia K.
    Ovaa, Huib
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (52) : 10149 - 10153
  • [7] Sensitivity-Enhanced NMR Reveals Alterations in Protein Structure by Cellular Milieus
    Frederick, Kendra K.
    Michaelis, Vladimir K.
    Corzilius, Bjoern
    Ong, Ta-Chung
    Jacavone, Angela C.
    Griffin, Robert G.
    Lindquist, Susan
    [J]. CELL, 2015, 163 (03) : 620 - 628
  • [8] In-Cell NMR and EPR Spectroscopy of Biomacromolecules
    Haensel, Robert
    Luh, Laura M.
    Corbeski, Ivan
    Trantirek, Lukas
    Doetsch, Volker
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (39) : 10300 - 10314
  • [9] Hansel R., 2014, ANGEW CHEM, V126, P10466
  • [10] 3D NMR spectroscopy for resonance assignment and structure elucidation of proteins under MAS: novel pulse schemes and sensitivity considerations
    Heise, H
    Seidel, K
    Etzkorn, M
    Becker, S
    Baldus, M
    [J]. JOURNAL OF MAGNETIC RESONANCE, 2005, 173 (01) : 64 - 74