Powiadomienia systemowe
- Sesja wygasła!
Tytuł artykułu
Treść / Zawartość
Pełne teksty:
Identyfikatory
Warianty tytułu
Monitoring of cellular metabolism by NMR spectroskopy
Języki publikacji
Abstrakty
Metabolomics approaches allow systematic identification and quantitation of all metabolites in biological samples analyzes. As already known metabolism is directly or indirectly related to every aspect of cell function, therefore a careful observation of every changes taking place in metabolism, for example endogenous biochemical reaction products, reflectsthe phenotype of any living cell. Monitoring the metabolite profiles using metabolomics technologies, especially nuclear magnetic resonance (NMR) spectroscopy based on cell culture, allows us to evaluate drug efficiency and outcome of experimental therapy, and most importantly, it allows us to monitor the reaction of the model cell lines to a given treatment. The continued development of metabolomic approaches, e.g. analytical technique, or chemometric software, will accelerate the widespread use of metabolomics not only in the clinical field but also in different biological fields. This work presents a use of nuclear magnetic resonance to characterize and understand the cellular metabolome in a wide range of pathophysiological and clinical contexts.
Wydawca
Czasopismo
Rocznik
Tom
Strony
323--333
Opis fizyczny
Bibliogr. 25 poz., rys.
Twórcy
autor
- studentka Katedry Biochemii, Biologii Molekularnej i Biotechnologii, Wydział Chemiczny, Politechnika Wrocławska, Wybrzeże Wyspiańskiego 27, 50-370 Wrocław
autor
- studentka Katedry Biochemii, Biologii Molekularnej i Biotechnologii, Wydział Chemiczny, Politechnika Wrocławska, Wybrzeże Wyspiańskiego 27, 50-370 Wrocław
autor
- Katedra Biochemii, Biologii Molekularnej i Biotechnologii, Wydział Chemiczny, Politechnika Wrocławska, Wybrzeże Wyspiańskiego 27, 50-370 Wrocław
Bibliografia
- [1] S.G. Oliver, M.K. Winson, D.B. Kell, F. Baganz, Trends Biotechnol., 1998, 16, 373.
- [2] R. Goodacre, J. Nutr., 2007, 137, 259.
- [3] A. Zhang, H. Sun, P. Wang, Y. Han, X. Wang, J. Proteomics, 2012, 75, 1079.
- [4] A.K. Arakaki, J. Skolnick, J.F. McDonald, Nature, 2008, 456, 443.
- [5] K.A. Mielko, N. Pudełko-Malik, A. Tarczewska, M. Piotr, Sustain. Chem. Pharm., 2021, 22, 100474.
- [6] J.K. Nicholson, I.D. Wilson, Prog. Nucl. Magn. Reson. Spectrosc., 1989, 21, 449.
- [7] A.A. Crook, R. Powers, Molecules, 2020, 25, 5128.
- [8] O. Beckonert, H.C. Keun, T.M.D. Ebbels, J. Bundy, E. Holmes, J.C. Lindon, J.K. Nicholson, Nat. Protoc., 2007, 2, 2692.
- [9] R. Ahmed, P.C. Varras, M.G. Siskos, H. Siddiqui, M.I. Choudhary, I.P. Gerothanassis, Molecules, 2020, 25, 4902.
- [10] E. Alexandri, R. Ahmed, H. Siddiqui, M.I. Choudhary, C.G. Tsiafoulis, I.P. Gerothanassis, Molecules, 2017, 22, 1663.
- [11] S. Deja, A. Litarski, K. A. Mielko, N. Pudełko-Malik, W. Wojtowicz, A. Zabek, T. Szydełko, P. Młynarz, “Gender-Specific Metabolomics Approach to Kidney Cancer,” 2021, 11, 767.
- [12] J.R. Masters, G.N. Stacey, Nat. Protoc., 2007, 2, 2276.
- [13] M. Ravi, V. Paramesh, S.R. Kaviya, E. Anuradha, F.D. Paul Solomon, J. Cell. Physiol., 2015, 230, 16.
- [14] B.D. Bennett, J. Yuan, E.H. Kimball, J.D. Rabinowitz, Nat. Protoc., 2008, 3, 1299.
- [15] U. Hofmann, K. Maier, A. Niebel, G. Vacun, M. Reuss, K. Mauch, Biotechnol. Bioeng., 2008, 100, 344.
- [16] Q. Teng, W. Huang, T.W. Collette, D.R. Ekman, C. Tan, Metabolomics, 2009, 5, 199.
- [17] C.A. Sellick, R. Hansen, A.R. Maqsood, W.B. Dunn, G.M. Stephens, R. Goodacre, A.J. Dickson, Anal. Chem., 2009, 81, 174.
- [18] U. Batista, M. Garvas, M. Nemec, M. Schara, P. Veranič, T. Koklic, Cell Biol. Int., 2010, 34, 663.
- [19] A. Artati, C. Prehn, J. Adamski, Methods Mol. Biol., 2019, 1994, 119.
- [20] S. Dietmair, N.E. Timmins, P.P. Gray, L.K. Nielsen, J.O. Krömer, Methods Mol. Biol., 2010, 404, 155.
- [21] J. Leenders, M. Frédérich, P. De Tullio, Drug Discov. Today Technol., 2015, 13, 39.
- [22] W. Xu, D. Lin, C. Huang, Acta Biochim. Biophys. Sin. (Shanghai)., 2017, 7, 617.
- [23] M. Vermathen, L.E.H. Paul, G. Diserens, P. Vermathen, J. Furrer, 1H HR-MAS NMR Based Metabolic Profiling of Cells in Response to Treatment with a Hexacationic Ruthenium 3 Metallaprism as Potential Anticancer Drug" PLoS One, [29.05.2015], https://pubmed.ncbi.nlm.nih.gov/26024484/.
- [24] S. Tiziani, A. Lodi, F.L. Khanim, M.R. Viant, C.M. Bunce, and U.L. Günther, PLoS One, 2009, 4, 1.
- [25] W. Wojtowicz, A. Wróbel, K. Puziak, R. Tarkowski, A. Balcerzak, M. Bębenek, P. Młynarz Metabolites, 2020, 10, 1.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-95fae0e6-3b85-4f8c-ba25-c4af1ad8ed62