Investigating Protein–Ligand Interactions by Solution Nuclear Magnetic Resonance Spectroscopy
Open accessAbstract
Protein–ligand interactions are of fundamental importance in almost all processes in living organisms. The ligands comprise small molecules, drugs or biological macromolecules and their interaction strength varies over several orders of magnitude. Solution NMR spectroscopy offers a large repertoire of techniques to study such complexes. Here, we give an overview of the different NMR approaches available. The information they provide ranges from the simple information about the presence of binding or epitope mapping to the complete 3 D structure of the complex. NMR spectroscopy is particularly useful for the study of weak interactions and for the screening of binding ligands with atomic resolution.
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NMR spectroscopy has a long-standing history of being used to effectively detect and measure a wide range of protein-ligand interactions, applicable in high-throughput fashion.
“An example of the employment of NMR in functional analysis is the detection of protein–metabolite interactions, in fact NMR spectroscopy has a long-standing history of being used to effectively detect and measure a wide range of protein–ligand interactions,144–146 which is also applicable in a high-throughput fashion.”
From Connecting metabolome and phenotype: recent advances in functional metabolomics tools for the identification of bioactive natural products (2024) · cites this paper as [144]
The Introduction (page unavailable) describes NMR as an efficient way to investigate protein–ligand interactions across a wide range of partners and says it allows fast screening. The Summary and Outlook (page unavailable) likewise describes techniques for weakly and tightly bound ligands. The paper does not establish the claim’s more specific high-throughput applicability; fast screening alone does not demonstrate high throughput. (LLM, conf=0.82)
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Cites
Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of Functionality
Sletten, E. M., & Bertozzi, C. R. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200900942 · Cited by 3,165 · see citing works
Pervushin, K. V., Riek, R., Wider, G., & Kurt Wüthrich, A. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.23.12366 · Cited by 2,450 · see citing works
Discovering High-Affinity Ligands for Proteins: SAR by NMR
Shuker, S. B., Hajduk, P. J., Meadows, R. P., & Fesik, S. W. (1996) · Science · doi:10.1126/science.274.5292.1531 · Cited by 2,045 · see citing works
Tjandra, N., & Bax, A. (1997) · Science · doi:10.1126/science.278.5340.1111 · Cited by 1,720 · see citing works
Expanding the Genetic Code of Escherichia coli
Wang, L., Brock, A., Herberich, B., & Schultz, P. G. (2001) · Science · doi:10.1126/science.1060077 · Cited by 1,504 · see citing works
Using chemical shift perturbation to characterise ligand binding
Williamson, M. P. (2013) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2013.02.001 · Cited by 1,471 · see citing works
Structure-Based Virtual Screening for Drug Discovery: Principles, Applications and Recent Advances
Lionta, E., Spyrou, G. M., Vassilatis, D. K., & Cournia, Z. (2014) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026614666140929124445 · Cited by 1,220 · see citing works
NMR Spectroscopy Techniques for Screening and Identifying Ligand Binding to Protein Receptors
Meyer, B., & Peters, T. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200390233 · Cited by 1,042 · see citing works
Pervushin, K. V., Riek, R., Wider, G., & Kurt Wüthrich, A. (2021) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789811235795_0006 · Cited by 951 · see citing works
The maximal affinity of ligands
Kuntz, I. D., Chen, K., Sharp, K. A., & Kollman, P. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.9997 · Cited by 859 · see citing works
Conformational entropy in molecular recognition by proteins
Frederick, K. K., Marlow, M. S., Valentine, K. G., & Wand, A. J. (2007) · Nature · doi:10.1038/nature05959 · Cited by 663 · see citing works
Tugarinov, V., Hwang, P. M., Ollerenshaw, J. E., & Kay, L. E. (2003) · Journal of the American Chemical Society · doi:10.1021/ja030153x · Cited by 651 · see citing works
Zwahlen, C., Legault, P., Vincent, S. J. F., Greenblatt, J., Konrat, R., & Kay, L. E. (1997) · Journal of the American Chemical Society · doi:10.1021/ja970224q · Cited by 606 · see citing works
THE USE OF 2 H, 13 C, 15 N MULTIDIMENSIONAL NMR GTO STUDY THE STRUCTURE AND DYNAMICS OF PROTEINS
Gardner, K. H., & Kay, L. E. (1998) · Annual Review of Biophysics and Biomolecular Structure · doi:10.1146/annurev.biophys.27.1.357 · Cited by 600 · see citing works
WaterLOGSY as a method for primary NMR screening: Practical aspects and range of applicability
Dalvit, C., Fogliatto, G., Stewart, A., Veronesi, M., & Stockman, B. J. (2001) · Journal of Biomolecular NMR · doi:10.1023/a:1013302231549 · Cited by 570 · see citing works
Bioorthogonale Chemie – oder: in einem Meer aus Funktionalität nach Selektivität fischen
Sletten, E. M., & Bertozzi, C. R. (2009) · Angewandte Chemie · doi:10.1002/ange.200900942 · Cited by 564 · see citing works
A Solution-Phase Chemical Approach to a New Crystal Structure of Cobalt
Dinega, D. P., & Bawendi, M. G. (1999) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(19990614)38:12 · Cited by 526 · see citing works
Order matrix analysis of residual dipolar couplings using singular value decomposition.
Losonczi, J., Andrec, M., Fischer, M. W. F., & Prestegard, J. (1999) · Journal of magnetic resonance (San Diego, Calif. 1997 : Print) · doi:10.1006/jmre.1999.1754 · Cited by 522 · see citing works
Optimal isotope labelling for NMR protein structure determinations
Kainosho, M., Torizawa, T., Iwashita, Y., Terauchi, T., Ono, A. M., & Güntert, P. (2006) · Nature · doi:10.1038/nature04525 · Cited by 485 · see citing works
Dalvit, C., Pevarello, P., Tatò, M., Veronesi, M., Vulpetti, A., & Sundström, M. (2000) · Journal of Biomolecular NMR · doi:10.1023/a:1008354229396 · Cited by 470 · see citing works
Magnetically-oriented phospholipid micelles as a tool for the study of membrane-associated molecules
Sanders, C. R., Hare, B. J., Howard, K. P., & Prestegard, J. H. (1994) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/0079-6565(94)80012-x · Cited by 420 · see citing works
Clore, G. M., & Gronenborn, A. M. (1982) · Journal of Magnetic Resonance (1969) · doi:10.1016/0022-2364(82)90073-7 · Cited by 403 · see citing works
Hajduk, P. J., Olejniczak, E. T., & Fesik, S. W. (1997) · Journal of the American Chemical Society · doi:10.1021/ja9715962 · Cited by 372 · see citing works
Quantitative NMR spectroscopy in pharmaceutical applications
Holzgrabe, U. (2010) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2010.05.001 · Cited by 364 · see citing works
Otting, G., & Wüthrich, K. (1990) · Quarterly Reviews of Biophysics · doi:10.1017/s0033583500005412 · Cited by 354 · see citing works
Zangger, K. (2015) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2015.02.002 · Cited by 337 · see citing works
Self-citationOtting, G., & Wuethrich, K. (1989) · Journal of the American Chemical Society · doi:10.1021/ja00187a050 · Cited by 314 · see citing works
A novel NMR method for determining the interfaces of large protein-protein complexes.
Shimada, I., Takahashi, H., Nakanishi, T., Kami, K., & Arata, Y. (2000) · Nature Structural Biology · doi:10.1038/73331 · Cited by 312 · see citing works
Current applications of 19F NMR to studies of protein structure and dynamics
Kitevski-LeBlanc, J. L., & Prosser, R. S. (2011) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2011.06.003 · Cited by 295 · see citing works
Recent developments in transferred NOE methods
Ni, F. (1994) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/0079-6565(94)90000-0 · Cited by 290 · see citing works
Clore, G. M., & Gronenborn, A. M. (1983) · Journal of Magnetic Resonance (1969) · doi:10.1016/0022-2364(83)90215-9 · Cited by 287 · see citing works
Direct Proline‐Catalyzed Asymmetric α‐Aminoxylation of Ketones
Hayashi, Y., Yamaguchi, J., Sumiya, T., & Shoji, M. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200353085 · Cited by 278 · see citing works
Spiteri, C., & Moses, J. E. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200905322 · Cited by 246 · see citing works
Solution NMR of Paramagnetic Molecules
(2016) · Elsevier eBooks · doi:10.1016/c2013-0-18690-4 · Cited by 242 · see citing works
A Graphene‐Based Platform for the Assay of Duplex‐DNA Unwinding by Helicase
Jang, H., Kim, Y., Kwon, H., Yeo, W., Kim, D., & Min, D. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.201001332 · Cited by 241 · see citing works
NMR studies of water bound to biological molecules
Otting, G. (1997) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/s0079-6565(97)00012-5 · Cited by 231 · see citing works
Gossert, A. D., & Jahnke, W. (2016) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2016.09.001 · Cited by 229 · see citing works
Identification of Protein Surfaces by NMR Measurements with a Paramagnetic Gd(III) Chelate
Pintacuda, G., & Otting, G. (2001) · Journal of the American Chemical Society · doi:10.1021/ja016985h · Cited by 216 · see citing works
Virus−Ligand Interactions: Identification and Characterization of Ligand Binding by NMR Spectroscopy
Benie, A. J., Moser, R., Bäuml, E., Blaas, D., & Peters, T. (2002) · Journal of the American Chemical Society · doi:10.1021/ja027691e · Cited by 215 · see citing works
New frontiers and developing applications in 19F NMR
Yu, J.-X., Hallac, R. R., Chiguru, S., & Mason, R. P. (2012) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2012.10.001 · Cited by 198 · see citing works
An Antibody Binding Site on Cytochrome C Defined by Hydrogen Exchange and Two-Dimensional NMR
Paterson, Y. Y. W., Englander, S. W., & Röder, H. (1990) · Science · doi:10.1126/science.1697101 · Cited by 186 · see citing works
Complete Assignment of Heteronuclear Protein Resonances by Protonless NMR Spectroscopy
Bermel, W., Bertini, I., Duma, L., Felli, I. C., Emsley, L., Pierattelli, R., & Vasos, P. R. (2005) · Angewandte Chemie International Edition · doi:10.1002/anie.200461794 · Cited by 183 · see citing works
Biosynthesis of Proteins Incorporating a Versatile Set of Phenylalanine Analogues
Kirshenbaum, K., Carrico, I. S., & Tirrell, D. A. (2002) · ChemBioChem · doi:10.1002/1439-7633(20020301)3:2/3 · Cited by 172 · see citing works
The INPHARMA Method: Protein‐Mediated Interligand NOEs for Pharmacophore Mapping
Sánchez‐Pedregal, V. M., Reese, M., Meiler, J., Blommers, M. J. J., Griesinger, C., & Carlomagno, T. (2005) · Angewandte Chemie International Edition · doi:10.1002/anie.200500503 · Cited by 170 · see citing works
Pseudocontact shifts in biomolecular NMR using paramagnetic metal tags
Nitsche, C., & Otting, G. (2016) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2016.11.001 · Cited by 167 · see citing works
NMR‐Techniken zum Screening und zur Identifizierung der Bindung von Liganden an Proteinrezeptoren
Meyer, B., & Peters, T. (2003) · Angewandte Chemie · doi:10.1002/ange.200390202 · Cited by 150 · see citing works
Applications of saturation transfer difference NMR in biological systems
Bhunia, A., Bhattacharjya, S., & Chatterjee, S. (2011) · Drug Discovery Today · doi:10.1016/j.drudis.2011.12.016 · Cited by 137 · see citing works
Luy, B., Kobzar, K. M., & Kessler, H. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200352860 · Cited by 137 · see citing works
Pintacuda, G., Park, A. Y., Keniry, M. A., Dixon, N. E., & Otting, G. (2006) · Journal of the American Chemical Society · doi:10.1021/ja057008z · Cited by 135 · see citing works
Arai, M., Ferreon, J. C., & Wright, P. E. (2012) · Journal of the American Chemical Society · doi:10.1021/ja209936u · Cited by 135 · see citing works
Hydrogen exchange and protein folding
Clarke, J., & Itzhaki, L. S. (1998) · Current Opinion in Structural Biology · doi:10.1016/s0959-440x(98)80018-3 · Cited by 121 · see citing works
Mapping the Orientation of Helices in Micelle-Bound Peptides by Paramagnetic Relaxation Waves
Respondek, M., Madl, T., Göbl, C., Golser, R., & Zangger, K. (2007) · Journal of the American Chemical Society · doi:10.1021/ja069004f · Cited by 121 · see citing works
Self-citationStructural Basis for Nucleic Acid and Toxin Recognition of the Bacterial Antitoxin CcdA
Madl, T., Melderen, L. V., Mine, N., Respondek, M., Oberer, M., Keller, W., Khatai, L., & Zangger, K. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.08.082 · Cited by 120 · see citing works
Self-citationBalaram, P., Bothner‐By, A. A., & Breslow, E. (1972) · Journal of the American Chemical Society · doi:10.1021/ja00766a064 · Cited by 118 · see citing works
Quantification of the Cellular Uptake of Cell‐Penetrating Peptides by MALDI‐TOF Mass Spectrometry
Burlina, F., Sagan, S., Bolbach, G., & Chassaing, G. (2005) · Angewandte Chemie International Edition · doi:10.1002/anie.200500477 · Cited by 117 · see citing works
Estimating Protein−Ligand Binding Affinity Using High-Throughput Screening by NMR
Shortridge, M. D., Hage, D. S., Harbison, G. S., & Powers, R. (2008) · Journal of Combinatorial Chemistry · doi:10.1021/cc800122m · Cited by 111 · see citing works
Quantitative analysis of protein–ligand interactions by NMR
Furukawa, A., Konuma, T., Yanaka, S., & Sugase, K. (2016) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2016.02.002 · Cited by 111 · see citing works
Nakanishi, T., Miyazawa, M., Sakakura, M., Terasawa, H., Takahashi, H. K., & Shimada, I. (2002) · Journal of Molecular Biology · doi:10.1016/s0022-2836(02)00018-9 · Cited by 110 · see citing works
Mari, S., Serrano‐Gómez, D., Cañada, F. J., Corbí, A. L., & Jiménez‐Barbero, J. (2004) · Angewandte Chemie International Edition · doi:10.1002/anie.200461574 · Cited by 105 · see citing works
Small-Molecule Binding Sites on Proteins Established by Paramagnetic NMR Spectroscopy
Guan, J., Keizers, P. H. J., Liu, W.-M., Löhr, F., Skinner, S. P., Heeneman, E. A., Schwalbe, H., Ubbink, M., & Siegal, G. (2013) · Journal of the American Chemical Society · doi:10.1021/ja401323m · Cited by 100 · see citing works
Brutscher, B., Felli, I. C., Gil‐Caballero, S., Hošek, T., Kümmerle, R., Piai, A., Pierattelli, R., & Sólyom, Z. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-20164-1_3 · Cited by 100 · see citing works
Applications of 19F-NMR in Fragment-Based Drug Discovery
Norton, R. S., Leung, E. W. W., Chandrashekaran, I. R., & MacRaild, C. A. (2016) · Molecules · doi:10.3390/molecules21070860 · Cited by 100 · see citing works
Madl, T., Bermel, W., & Zangger, K. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200902561 · Cited by 93 · see citing works
Self-citationProtein interaction patterns in different cellular environments are revealed by in-cell NMR
Barbieri, L., Luchinat, E., & Banci, L. (2015) · Scientific Reports · doi:10.1038/srep14456 · Cited by 93 · see citing works
Bolon, P. J., Al‐Hashimi, H. M., & Prestegard, J. H. (1999) · Journal of Molecular Biology · doi:10.1006/jmbi.1999.3133 · Cited by 80 · see citing works
Screening of Small Molecule Interactor Library by Using In-Cell NMR Spectroscopy (SMILI-NMR)
Xie, J., Thapa, R., Reverdatto, S., Burz, D. S., & Shekhtman, A. G. (2009) · Journal of Medicinal Chemistry · doi:10.1021/jm9000743 · Cited by 79 · see citing works
Structural Analysis of Large Protein Complexes Using Solvent Paramagnetic Relaxation Enhancements
Madl, T., Guettler, T., Görlich, D., & Sattler, M. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201007168 · Cited by 78 · see citing works
Novel methods based on 13C detection to study intrinsically disordered proteins
Felli, I. C., & Pierattelli, R. (2014) · Journal of Magnetic Resonance · doi:10.1016/j.jmr.2013.10.020 · Cited by 76 · see citing works
Assadi‐Porter, F. M., Tonelli, M., Maillet, É. L., Hallenga, K., Benard, O., Max, M., & Markley, J. L. (2008) · Journal of the American Chemical Society · doi:10.1021/ja8016939 · Cited by 75 · see citing works
Reliable high-throughput functional screening with 3-FABS
Dalvit, C., Ardini, E., Fogliatto, G., Mongelli, N., & Veronesi, M. (2004) · Drug Discovery Today · doi:10.1016/s1359-6446(04)03161-7 · Cited by 64 · see citing works
Felli, I. C., & Pierattelli, R. (2012) · IUBMB Life · doi:10.1002/iub.1045 · Cited by 62 · see citing works
Spiteri, C., & Moses, J. E. (2009) · Angewandte Chemie · doi:10.1002/ange.200905322 · Cited by 61 · see citing works
Studying the Structure and Dynamics of Biomolecules by Using Soluble Paramagnetic Probes
Hocking, H. G., Zangger, K., & Madl, T. (2013) · ChemPhysChem · doi:10.1002/cphc.201300219 · Cited by 61 · see citing works
Self-citationSERF Protein Is a Direct Modifier of Amyloid Fiber Assembly
Falsone, S. F., Meyer, N. H., Schrank, E., Leitinger, G., Pham, C. L., Fodero-Tavoletti, M., Holmberg, M. A., Dulle, M., Scicluna, B. J., Gesslbauer, B., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.06.012 · Cited by 61 · see citing works
Self-citationReuben, J., & LEIGH, J. S. J. (1972) · Journal of the American Chemical Society · doi:10.1021/ja00763a042 · Cited by 59 · see citing works
A Graphene‐Based Platform for the Assay of Duplex‐DNA Unwinding by Helicase
Jang, H., Kim, Y., Kwon, H., Yeo, W., Kim, D., & Min, D. (2010) · Angewandte Chemie · doi:10.1002/ange.201001332 · Cited by 58 · see citing works
An NMR strategy for fragment-based ligand screening utilizing a paramagnetic lanthanide probe
Saio, T., Ogura, K., Shimizu, K., Yokochi, M., Burke, T. R., & Inagaki, F. (2011) · Journal of Biomolecular NMR · doi:10.1007/s10858-011-9566-5 · Cited by 57 · see citing works
Koenig, B. W., Mitchell, D. C., König, S., Grzesiek, S., Litman, B. J., & Bax, A. (2000) · Journal of Biomolecular NMR · doi:10.1023/a:1008378523816 · Cited by 54 · see citing works
Positioning of Micelle-Bound Peptides by Paramagnetic Relaxation Enhancements
Zangger, K., Respondek, M., Göbl, C., Hohlweg, W., Rasmussen, K., Grampp, G., & Madl, T. (2009) · The Journal of Physical Chemistry B · doi:10.1021/jp808501x · Cited by 50 · see citing works
Self-citationCanales, Á., Rodríguez‐Salarichs, J., Trigili, C., Nieto, L., Coderch, C., Andreu, J. M., Paterson, I., Jiménez‐Barbero, J., & Díaz, J. F. (2011) · ACS Chemical Biology · doi:10.1021/cb200099u · Cited by 50 · see citing works
Luy, B., Kobzar, K. M., & Kessler, H. (2004) · Angewandte Chemie · doi:10.1002/ange.200352860 · Cited by 48 · see citing works
Unione, L., Galante, S., Díaz, D., Cañada, F. J., & Jiménez‐Barbero, J. (2014) · MedChemComm · doi:10.1039/c4md00138a · Cited by 48 · see citing works
Martín‐Santamaría, S., André, S., Buzamet, E., Caraballo, R., Fernández‐Cureses, G., Morando, M. A., Ribeiro, J. P., Ramírez‐Gualito, K., de Pascual‐Teresa, B., Cañada, F. J., et al. (2011) · Organic & Biomolecular Chemistry · doi:10.1039/c0ob01235a · Cited by 48 · see citing works
The INPHARMA Method: Protein‐Mediated Interligand NOEs for Pharmacophore Mapping
Sánchez‐Pedregal, V. M., Reese, M., Meiler, J., Blommers, M. J. J., Griesinger, C., & Carlomagno, T. (2005) · Angewandte Chemie · doi:10.1002/ange.200500503 · Cited by 48 · see citing works
Meyer, N. H., & Zangger, K. (2013) · Chemical Communications · doi:10.1039/c3cc48135b · Cited by 45 · see citing works
Self-citationNMR in natural products: understanding conformation, configuration and receptor interactions
Carlomagno, T. (2012) · Natural Product Reports · doi:10.1039/c2np00098a · Cited by 40 · see citing works
Complete Assignment of Heteronuclear Protein Resonances by Protonless NMR Spectroscopy
Bermel, W., Bertini, I., Duma, L., Felli, I. C., Emsley, L., Pierattelli, R., & Vasos, P. R. (2005) · Angewandte Chemie · doi:10.1002/ange.200461794 · Cited by 40 · see citing works
Identification of a protein-binding surface by differential amide hydrogen-exchange measurements
Werner, M. H., & Wemmer, D. E. (1992) · Journal of Molecular Biology · doi:10.1016/0022-2836(92)90407-b · Cited by 37 · see citing works
Wildes, D. P., & Marqusee, S. (2004) · Protein Science · doi:10.1110/ps.04990205 · Cited by 36 · see citing works
Glanzer, S., Pulido, S., Tutz, S., Wagner, G. E., Kriechbaum, M., Gubensäk, N., Trifunović, J., Dorn, M., Fabian, W. M. F., Novak, P., et al. (2015) · Chemistry - A European Journal · doi:10.1002/chem.201406413 · Cited by 35 · see citing works
Self-citationDetection of intermolecular NOE interactions in large protein complexes
Anglister, J., Srivastava, G., & Naider, F. R. (2016) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/j.pnmrs.2016.08.002 · Cited by 35 · see citing works
Mari, S., Serrano‐Gómez, D., Cañada, F. J., Corbí, A. L., & Jiménez‐Barbero, J. (2004) · Angewandte Chemie · doi:10.1002/ange.200461574 · Cited by 34 · see citing works
Probing the Interactions of Macrolide Antibiotics with Membrane-Mimetics by NMR Spectroscopy
Kosol, S., Schrank, E., Krajačić, M. B., Wagner, G. E., Meyer, N. H., Göbl, C., Rechberger, G. N., Zangger, K., & Novak, P. (2012) · Journal of Medicinal Chemistry · doi:10.1021/jm300647f · Cited by 33 · see citing works
Self-citationRibeiro, J. P., André, S., Cañada, F. J., Gabius, H., Butera, A. P., Alves, R. J., & Jiménez‐Barbero, J. (2010) · ChemMedChem · doi:10.1002/cmdc.200900476 · Cited by 32 · see citing works
Visualizing an Ultra‐Weak Protein–Protein Interaction in Phosphorylation Signaling
Xing, Q., Huang, P., Yang, J. H., Sun, J., Gong, Z., Xu, D., Guo, D., Chen, S., Yang, Y., Wang, Y., et al. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201405976 · Cited by 31 · see citing works
Pershina, L., & Hvidt, A. (1974) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1974.tb03774.x · Cited by 28 · see citing works
Studies of lysozyme binding to histamine as a ligand for hydrophobic charge induction chromatography
Shi, Q., Shen, F., & Sun, S. (2009) · Biotechnology Progress · doi:10.1002/btpr.295 · Cited by 25 · see citing works
Cross-saturation and transferred cross-saturation experiments
Ueda, T., Takeuchi, K., Nishida, N., Stampoulis, P., Kofuku, Y., Osawa, M., & Shimada, I. (2014) · Quarterly Reviews of Biophysics · doi:10.1017/s0033583514000043 · Cited by 22 · see citing works
Koculi, E., Horst, R., Horwich, A. L., & Kurt Wüthrich, A. (2011) · Protein Science · doi:10.1002/pro.665 · Cited by 21 · see citing works
Stickstoffmonoxid: die rätselhafte Chemie eines biologischen Botenstoffes
Pfeiffer, S., Mayer, B., & Hemmens, B. (1999) · Angewandte Chemie · doi:10.1002/(sici)1521-3757(19990614)111:12 · Cited by 18 · see citing works
Madl, T., Bermel, W., & Zangger, K. (2009) · Angewandte Chemie · doi:10.1002/ange.200902561 · Cited by 17 · see citing works
Self-citationBrandt, P., & Woodward, C. K. (1987) · Biochemistry · doi:10.1021/bi00385a032 · Cited by 17 · see citing works
Hydrogen exchange kinetics changes upon formation of the soybean trypsin inhibitor-trypsin complex
Woodward, C. K., & Ellis, L. M. (1975) · Biochemistry · doi:10.1021/bi00686a020 · Cited by 16 · see citing works
Martinez‐Farina, C. F., McCormick, N. E., Robertson, A. W., Clement, H. A., Jee, A., Ampaw, A. A., Chan, N., Syvitski, R. T., & Jakeman, D. L. (2015) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob01508a · Cited by 15 · see citing works
X-filtering for a range of coupling constants: application to the detection of intermolecular NOEs
Zangger, K., Oberer, M., Keller, W., & Sterk, H. (2003) · Journal of Magnetic Resonance · doi:10.1016/s1090-7807(02)00176-3 · Cited by 14 · see citing works
Self-citationNakamura, T., Takahashi, H. K., Takahashi, M., Shimba, N., Suzuki, E., & Shimada, I. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm901099v · Cited by 12 · see citing works
Structural Analysis of Large Protein Complexes Using Solvent Paramagnetic Relaxation Enhancements
Madl, T., Guettler, T., Görlich, D., & Sattler, M. (2011) · Angewandte Chemie · doi:10.1002/ange.201007168 · Cited by 10 · see citing works
Weimar, T., Petersen, B. O., Svensson, B., & Pinto, B. M. (2000) · Carbohydrate Research · doi:10.1016/s0008-6215(00)00021-5 · Cited by 7 · see citing works
Visualizing an Ultra‐Weak Protein–Protein Interaction in Phosphorylation Signaling
Xing, Q., Huang, P., Yang, J. H., Sun, J., Gong, Z., Xu, D., Guo, D., Chen, S., Yang, Y., Wang, Y., et al. (2014) · Angewandte Chemie · doi:10.1002/ange.201405976 · Cited by 4 · see citing works
Flagged first, then by citations
1 of the 110 references couldn’t be matched to a known paper.
Research works printed but not linked: 17
- S. Martín-Santamaría, S. André, E. Buzamet, R. Caraballo, G. Fernández-Cureses, M. Morando, J. P. Ribeiro, K. Ramírez-Gualito, B. de Pascual-Teresa, F. J. Cañada, M. Menendez, O. Ramstrom, J. Jimenez-Barbero, D. Solis, H.-J. Gabius, Org. Biomol. Chem. 2011, 9, 5445– 5455; 21660340
- L. Unione, S. Galante, D. Díaz, F. J. Cañada, J. Jiménez-Barbero, MedChemComm 2014, 5, 1280– 1289.
- [40]F. M. Assadi-Porter, M. Tonelli, E. Maillet, K. Hallenga, O. Benard, M. Max, J. L. Markley, J. Am. Chem. Soc. 2008, 130, 7212– 7213. 18481853 PMC2759897
- [45]G. Otting, Prog. Nucl. Magn. Reson. Spectrosc. 1997, 31, 259– 285. 28283085
- [46]G. Otting, K. Wüthrich, J. Am. Chem. Soc. 1989, 111, 1871– 1875.
- [47]C. F. Martinez-Farina, N. McCormick, A. W. Robertson, H. Clement, A. Jee, A. Ampaw, N.-L. Chan, R. T. Syvitski, D. L. Jakeman, Org. Biomol. Chem. 2015, 13, 10324– 10327. 26309036
- [48]H. Takahashi, T. Nakanishi, K. Kami, Y. Arata, I. Shimada, Nat. Struct. Biol. 2000, 7, 220– 223. 10700281
- [51]D. Neuhaus, M. P. Williamson, The nuclear Overhauser effect in structural and conformational analysis, 2nd ed., Wiley-VCH, Weinheim, 2000.
- G. M. Clore, A. M. Gronenborn, J. Magn. Reson. 1983, 53, 423– 442;
- G. M. Clore, A. M. Gronenborn, J. Magn. Reson. 1982, 48, 402– 417;
- P. Balaram, A. A. Bothner-By, E. Breslow, J. Am. Chem. Soc. 1972, 94, 4017– 4018;5037990
- F. Ni, Prog. Nucl. Magn. Reson. Spectrosc. 1994, 26, 517– 606.
- V. M. Sánchez-Pedregal, M. Reese, J. Meiler, M. J. J. Blommers, C. Griesinger, T. Carlomagno, Angew. Chem. Int. Ed. 2005, 44, 4172– 4175; 15929149 Angew. Chem. 2005, 117, 4244– 4247.
- C. Zwahlen, P. Legault, S. J. F. Vincent, J. Greenblatt, R. Konrat, L. E. Kay, J. Am. Chem. Soc. 1997, 119, 6711– 6721;
- [59]P. J. Hajduk, E. T. Olejniczak, S. W. Fesik, J. Am. Chem. Soc. 1997, 119, 12257– 12261.
- [61]J. Reuben, J. S. Leigh, J. Am. Chem. Soc. 1972, 94, 2789– 2793.
- C. R. Sanders, B. J. Hare, K. P. Howard, J. H. Prestegard, Prog. Nucl. Magn. Reson. Spectrosc. 1994, 26, 421– 444;
Cited by
Sorted by citations
Fu, Y., Zhao, J., & Chen, Z. (2018) · Computational and Mathematical Methods in Medicine · doi:10.1155/2018/3502514 · Cited by 253 · see citing works
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Hanks, G. E., Hanlon, A., Pinover, W. H., Horwitz, E. M., & Schultheiss, T. E. (1999) · PubMed · Cited by 110 · see citing works
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Self-citationRotem‐Bamberger, S., Fahoum, J., Keinan‐Adamsky, K., Tsaban, T., Avraham, O., Shalev, D. E., Chill, J. H., & Schueler‐Furman, O. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102145 · Cited by 14 · see citing works
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Lucero, D. A., Cantoia, A., Sánchez‐López, C., Binolfi, A., Mogk, A., Ceccarelli, E. A., & Rosano, G. L. (2021) · FEBS Letters · doi:10.1002/1873-3468.14081 · Cited by 12 · see citing works
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Eraslan, Z., Cascante, M., & Günther, U. L. (2022) · Handbook of experimental pharmacology · doi:10.1007/164_2022_619 · Cited by 8 · see citing works
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Caccamo, M. T., Mavilia, G., Mavilia, L., Calandra, P., Lombardo, D., Magazù, S., Consiglio Nazionale delle Ricerche, I. P. L. S. M. N., & CNR–IPCF, I. P. I. P. C. F. –. (. M. V. F. S. D. (2020) · AIMS Biophysics · doi:10.3934/biophy.2020030 · Cited by 7 · see citing works
Stadler, K. A., Becker, W., Darnhofer, B., Birner‐Gruenberger, R., & Zangger, K. (2022) · Amino Acids · doi:10.1007/s00726-022-03148-2 · Cited by 7 · see citing works
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Gubensäk, N., Wagner, G. E., Schrank, E., Falsone, S. F., Berger, T. M. I., Pavkov‐Keller, T., Reidl, J., & Zangger, K. (2020) · Molecular Microbiology · doi:10.1111/mmi.14673 · Cited by 7 · see citing works
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Davis, B. J. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1197-5_11 · Cited by 6 · see citing works
Gubensäk, N., Schrank, E., Hartlmüller, C., Göbl, C., Falsone, S. F., Becker, W. F., Wagner, G. E., Pulido, S., Meyer, N. H., Pavkov‐Keller, T., et al. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.101167 · Cited by 5 · see citing works
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Mateos, B., Sealey‐Cardona, M., Balazs, K., Konrat, J., Staffler, G., & Konrat, R. (2019) · Angewandte Chemie · doi:10.1002/ange.201913585 · Cited by 5 · see citing works
Hőgye, F., Farkas, L. B., Balogh, Á. K., Szilágyi, L. S., Alnukari, S., Bajza, I., Borbás, A., Fehér, K., Illyés, T. Z., & Timári, I. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031742 · Cited by 5 · see citing works
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Babiyana, S., Balachandran, V., Thirughanasambantham, N., Viji, A., Narayana, B., & Salian, V. V. (2025) · Discover Chemistry. · doi:10.1007/s44371-025-00312-x · Cited by 5 · see citing works
Toscano, G., Rosati, M., Barbieri, L., Maier, K., Banci, L., Luchinat, E., Konrat, R., & Lichtenecker, R. J. (2024) · Chemical Communications · doi:10.1039/d4cc04789c · Cited by 4 · see citing works
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Kawale, A. A., & Burmann, B. M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-99127-8.00010-6 · Cited by 4 · see citing works
Wahongan, I. F., Suoth, E. J., Fatimawali, F., Alhumaid, S., Albayat, H., Aljeldah, M. M., Shammari, B. R. A., Mashraqi, M. M., Alshehri, A. A., Sulaiman, T., et al. (2022) · Vaccines · doi:10.3390/vaccines10101734 · Cited by 4 · see citing works
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Thalhammer, A., & Broeker, N. K. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2624-5_13 · Cited by 4 · see citing works
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Bag, S. S., Gogoi, H., Roy, S., Pradhan, M. K., & Talukdar, S. (2025) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2025.116290 · Cited by 3 · see citing works
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Berrino, E., Michelet, B., Martin‐Mingot, A., Carta, F., Supuran, C. T., & Thibaudeau, S. (2021) · Angewandte Chemie · doi:10.1002/ange.202103211 · Cited by 3 · see citing works
Voigt, B., Bhatia, T., Hesselbarth, J., Baumann, M., Schmidt, C., Ott, M., & Balbach, J. (2023) · ChemPhysChem · doi:10.1002/cphc.202300439 · Cited by 3 · see citing works
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Stadler, K. A., Ortiz-Joya, L. J., Singh, A., Buhlheller, C., Gruber, K. F., Pavkov‐Keller, T., O'Hagan, T. B., Guarné, A., Pulido, S., Marín‐Villa, M., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-59654-8 · Cited by 3 · see citing works
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Vega, M. C., & Fernández, F. J. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-52193-5 · Cited by 3 · see citing works
Lü, B., Liao, S.-M., Liang, S.-J., Peng, L., Li, J., Liu, X., Huang, R., & Zhou, G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094641 · Cited by 2 · see citing works
Saberi, M., Dekkers, R., Passerini, L., Huber, M., Overhand, M., & Ubbink, M. (2025) · Journal of Biomolecular NMR · doi:10.1007/s10858-025-00459-w · Cited by 2 · see citing works
- Authors
- Becker, W., Bhattiprolu, K. C., Gubensäk, N., & Zangger, K.
- Affiliations
- University of Graz (AT)
- Corresponding author
- Zangger, Klaus
- Venue
- ChemPhysChem
- Publisher
- Wiley
- Published
- 2018-02-16
- Volume
- 19
- Issue
- 8
- Pages
- 895-906
- ISSN
- 1439-4235 (ISSN-L)
- 1439-7641
- PMC
- PMC5915746
- OpenAlex
- W2782612584
- Cited by
- 138
- References
- 110
- Citations by year
- 2026: 9 · 2025: 12 · 2024: 24 · 2023: 13 · 2022: 21 · 2021: 21 · 2020: 16 · 2019: 15 · 2018: 6
- FWCI
- 1.82
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- ChemPhysChem (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Austrian Science Fund (P30230)
- Topics
- Physical Sciences › Chemistry › Spectroscopy › Advanced NMR Techniques and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Interaction Studies and Fluorescence Analysis
- Keywords
- protein-ligand interactions, solution NMR spectroscopy, weak interaction, ligand screening, complex structure determination, drug binding, binding strength
- MeSH terms
- Animals, Ligands, Protein Binding, Proteins, Nuclear Magnetic Resonance, Biomolecular
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