Critical evaluation of a crystal structure of nitrogenase with bound N


Journal

Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
ISSN: 1432-1327
Titre abrégé: J Biol Inorg Chem
Pays: Germany
ID NLM: 9616326

Informations de publication

Date de publication:
05 2021
Historique:
received: 21 01 2021
accepted: 10 02 2021
pubmed: 14 3 2021
medline: 7 9 2021
entrez: 13 3 2021
Statut: ppublish

Résumé

Recently, a 1.83 Å crystallographic structure of nitrogenase was suggested to show N

Identifiants

pubmed: 33713183
doi: 10.1007/s00775-021-01858-8
pii: 10.1007/s00775-021-01858-8
pmc: PMC8068654
doi:

Substances chimiques

Ligands 0
Nitrogenase EC 1.18.6.1
Nitrogen N762921K75

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

341-353

Références

Hoffman BM, Lukoyanov D, Yang Z-Y et al (2014) Mechanism of nitrogen fixation by nitrogenase: the next stage. Chem Rev 114:4041–4062. https://doi.org/10.1021/cr400641x
doi: 10.1021/cr400641x pubmed: 24467365 pmcid: 4012840
Thorneley RNF, Lowe DJ (1984) The mechanism of Klebsiella pneumoniae nitrogenase action. Pre-steady-state kinetics of an enzyme-bound intermediate in N
doi: 10.1042/bj2240887 pubmed: 6395862 pmcid: 1144525
Thorneley RNF, Lowe DJ (1985) Kinetics and mechanism of the nitrogenase enzyme system. In: Spiro TG (ed) Molybdenum enzymes. Wiley, New York, pp 221–284
Spatzal T, Aksoyoglu M, Zhang L et al (2011) Evidence for Interstitial Carbon in Nitrogenase FeMo cofactor. Science (80-) 120:940. https://doi.org/10.1126/science.1214025
doi: 10.1126/science.1214025
Einsle O, Rees DC (2020) Structural enzymology of nitrogenase enzymes. Chem Rev 120:4969–5004. https://doi.org/10.1021/acs.chemrev.0c00067
doi: 10.1021/acs.chemrev.0c00067 pubmed: 32538623
Spatzal T, Perez KA, Einsle O et al (2014) Ligand binding to the FeMo-cofactor: Structures of CO-bound and reactivated nitrogenase. Science 345:1620–1623. https://doi.org/10.1126/science.1256679
doi: 10.1126/science.1256679 pubmed: 25258081 pmcid: 4205161
Sippel D, Einsle O (2017) The structure of vanadium nitrogenase reveals an unusual bridging ligand. Nat Chem Biol 13:956–960. https://doi.org/10.1038/nchembio.2428
doi: 10.1038/nchembio.2428 pubmed: 28692069 pmcid: 5563456
Benediktsson B, Thorhallsson AT, Bjornsson R (2018) QM/MM calculations reveal a bridging hydroxo group in a vanadium nitrogenase crystal structure. Chem Commun 54:7310–7313. https://doi.org/10.1039/C8CC03793K
doi: 10.1039/C8CC03793K
Cao L, Caldararu O, Ryde U (2020) Does the crystal structure of vanadium nitrogenase contain a reaction intermediate? Evidence from quantum refinement. J Biol Inorg Chem 25:847–861. https://doi.org/10.1007/s00775-020-01813-z
doi: 10.1007/s00775-020-01813-z pubmed: 32856107 pmcid: 7511287
Varley JB, Wang Y, Chan K et al (2015) Mechanistic insights into nitrogen fixation by nitrogenase enzymes. Phys Chem Chem Phys 17:29541–29547. https://doi.org/10.1039/C5CP04034E
doi: 10.1039/C5CP04034E pubmed: 26366854
Cao L, Ryde U (2020) Putative reaction mechanism of nitrogenase after dissociation of a sulfide ligand. J Catal 391:247–259. https://doi.org/10.1016/j.jcat.2020.08.028
doi: 10.1016/j.jcat.2020.08.028
Kang W, Lee CC, Jasniewski AJ et al (2020) Structural evidence for a dynamic metallocofactor during N
doi: 10.1126/science.aaz6748
Ryde U, Olsen L, Nilsson K (2002) Quantum chemical geometry optimizations in proteins using crystallographic raw data. J Comput Chem 23:1058–1070. https://doi.org/10.1002/jcc.10093
doi: 10.1002/jcc.10093 pubmed: 12116392
Kang W, Lee CC, Jasniewski AJ et al (2020) Anomalous datasets for 6UG0 and 6VXT. Zenodo. https://doi.org/10.5281/zenodo.3756201
doi: 10.5281/zenodo.3756201
Kleywegt GJ, Jones TA (1997) Model building and refinement practice. Meth Enzym 227:208–230
doi: 10.1016/S0076-6879(97)77013-7
Engh RA, Huber R (1991) Accurate bond and angle parameters for X-ray protein structure refinement. Acta Crystallogr Sect A 47:392–400. https://doi.org/10.1107/S0108767391001071
doi: 10.1107/S0108767391001071
Pannu NS, Read RJ (1996) Improved structure refinement through maximum likelihood. Acta Crystallogr Sect A A52:659–668. https://doi.org/10.1107/S0108767396004370
doi: 10.1107/S0108767396004370
Adams PD, Pannu NS, Read RJ, Brünger AT (1997) Cross-validated maximum likelihood enhances crystallographic simulated annealing refinement. Proc Natl Acad Sci USA 94:5018–5023. https://doi.org/10.1073/pnas.94.10.5018
doi: 10.1073/pnas.94.10.5018 pubmed: 9144182
Kleywegt GJ (2007) Crystallographic refinement of ligand complexes. Acta Crystallogr Sect D 63:94–100. https://doi.org/10.1107/S0907444906022657
doi: 10.1107/S0907444906022657
Hu L, Ryde U (2011) Comparison of methods to obtain force-field parameters for metal sites. J Chem Theory Comput 7:2452–2463. https://doi.org/10.1021/ct100725a
doi: 10.1021/ct100725a pubmed: 26606619
Senn HM, Thiel W (2009) QM/MM methods for biomolecular systems. Angew Chem Int Ed 48:1198–1229. https://doi.org/10.1002/anie.200802019
doi: 10.1002/anie.200802019
Ryde U (2016) QM/MM calculations on proteins. Methods Enzymol 577:119–158. https://doi.org/10.1016/bs.mie.2016.05.014
doi: 10.1016/bs.mie.2016.05.014 pubmed: 27498637
Furche F, Ahlrichs R, Hättig C et al (2014) Turbomole. Wiley Interdiscip Rev Comput Mol Sci 4:91–100. https://doi.org/10.1002/wcms.1162
doi: 10.1002/wcms.1162
Brunger AT, Adams PD, Clore GM et al (1998) Crystallography & NMR system: a new software suite for macromolecular structure determination. Acta Crystallogr D 54:905–921. https://doi.org/10.1107/S0907444998003254
doi: 10.1107/S0907444998003254 pubmed: 9757107
Brunger AT (2007) Version 1.2 of the Crystallography and NMR system. Nat Protoc 2:2728–2733. https://doi.org/10.1038/nprot.2007.406
doi: 10.1038/nprot.2007.406 pubmed: 18007608
Tao J, Perdew JP, Staroverov VN, Scuseria GE (2003) Climbing the density functional ladder: non-empirical meta-generalized gradient approximation designed for molecules and solids. Phys Rev Lett 91:146401. https://doi.org/10.1103/PhysRevLett.91.146401
doi: 10.1103/PhysRevLett.91.146401 pubmed: 14611541
Weigend F, Ahlrichs R (2005) Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy. Phys Chem Chem Phys 7:3297–3305. https://doi.org/10.1039/b508541a
doi: 10.1039/b508541a
Eichkorn K, Treutler O, Öhm H et al (1995) Auxiliary basis-sets to approximate coulomb potentials. Chem Phys Lett 240:283–289. https://doi.org/10.1016/0009-2614(95)00621-a
doi: 10.1016/0009-2614(95)00621-a
Eichkorn K, Weigend F, Treutler O, Ahlrichs R (1997) Auxiliary basis sets for main row atoms and transition metals and their use to approximate Coulomb potentials. Theor Chem Acc 97:119–124. https://doi.org/10.1007/s002140050244
doi: 10.1007/s002140050244
Caldeweyher E, Bannwarth C, Grimme S (2017) Extension of the D3 dispersion coefficient model. J Chem Phys 147:34112. https://doi.org/10.1063/1.4993215
doi: 10.1063/1.4993215
Caldeweyher E, Ehlert S, Hansen A et al (2019) A generally applicable atomic-charge dependent London dispersion correction. J Chem Phys 150:154122. https://doi.org/10.1063/1.5090222
doi: 10.1063/1.5090222 pubmed: 31005066
Bjornsson R, Lima FA, Spatzal T et al (2014) Identification of a spin-coupled Mo(III) in the nitrogenase iron–molybdenum cofactor. Chem Sci 5:3096–3103. https://doi.org/10.1039/C4SC00337C
doi: 10.1039/C4SC00337C
Bjornsson R, Neese F, DeBeer S (2017) Revisiting the Mössbauer isomer shifts of the FeMoco cluster of nitrogenase and the cofactor charge. Inorg Chem 56:1470–1477. https://doi.org/10.1021/acs.inorgchem.6b02540
doi: 10.1021/acs.inorgchem.6b02540 pubmed: 28071903
Lovell T, Li J, Liu T et al (2001) FeMo cofactor of nitrogenase: a density functional study of states MN, Mox, MR, and MI. J Am Chem Soc 123:12392–12410. https://doi.org/10.1021/ja011860y
doi: 10.1021/ja011860y pubmed: 11734043
Cao L, Caldararu O, Ryde U (2018) Protonation and reduction of the FeMo cluster in nitrogenase studied by quantum mechanics/molecular mechanics (QM/MM) calculations. J Chem Theory Comput 14:6653–6678. https://doi.org/10.1021/acs.jctc.8b00778
doi: 10.1021/acs.jctc.8b00778 pubmed: 30354152
Cao L, Ryde U (2018) Influence of the protein and DFT method on the broken-symmetry and spin states in nitrogenase. Int J Quantum Chem 118:e25627. https://doi.org/10.1002/qua.25627
doi: 10.1002/qua.25627
Szilagyi RK, Winslow MA (2006) On the accuracy of density functional theory for iron—sulfur clusters. J Comput Chem 27:1385–1397. https://doi.org/10.1002/jcc.20449
doi: 10.1002/jcc.20449 pubmed: 16788911
Greco C, Fantucci P, Ryde U, de Gioia L (2011) Fast generation of broken-symmetry states in a large system including multiple iron–sulfur assemblies: Investigation of QM/MM energies, clusters charges, and spin populations. Int J Quantum Chem 111:3949–3960. https://doi.org/10.1002/qua.22849
doi: 10.1002/qua.22849
Tickle IJ, Sharff A, Flensburg C, et al (2020) The STARANISO/PDBpeep Server. http://staraniso.globalphasing.org/172cgi-bin/PDBpeep.cgi?crit=tism&tval=1.20&ID=6ug0 . Accessed 15 Dec 2020

Auteurs

Justin Bergmann (J)

Department of Theoretical Chemistry, Lund University, Chemical Centre, P. O. Box 124, 221 00, Lund, Sweden.

Esko Oksanen (E)

European Spallation Source ESS ERIC, Lund, Sweden.

Ulf Ryde (U)

Department of Theoretical Chemistry, Lund University, Chemical Centre, P. O. Box 124, 221 00, Lund, Sweden. Ulf.Ryde@teokem.lu.se.

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