BMDMS-NP: A comprehensive ESI-MS/MS spectral library of natural compounds

被引:12
|
作者
Lee, Sangwon [1 ,2 ]
Hwang, Sungbo [1 ,2 ]
Seo, Myungwon [1 ,2 ]
Shin, Ki Beom [1 ,2 ]
Kim, Kwang Hoe [3 ]
Park, Gun Wook [3 ]
Kim, Jin Young [3 ]
Yoo, Jong Shin [3 ,4 ]
No, Kyoung Tai [1 ,2 ]
机构
[1] Yonsei Univ, Dept Biotechnol, Seoul, South Korea
[2] Bioinformat & Mol Design Res Ctr, Incheon, South Korea
[3] Korea Basic Sci Inst, Res Ctr Bioconvergence Anal, Ochang, South Korea
[4] Chungnam Natl Univ, Grad Sch Analyt Sci & Technol, Daejeon, South Korea
关键词
Natural products; Metabolites; Tandem mass spectrum; Spectral library;
D O I
10.1016/j.phytochem.2020.112427
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Bioinformatics & Molecular Design Research Center Mass Spectral Library - Natural Products (BMDMS-NP) is a library containing the mass spectra of natural compounds, especially plant specialized metabolites. At present, the library contains the electrospray ionization tandem mass spectrometry (ESI-MS/MS) spectra of 2739 plant metabolites that are commercially available. The contents of the library were made comprehensive by incorporating data generated under various experimental conditions for compounds with diverse molecular structures. The structural diversity of the BMDMS-NP data was evaluated using molecular fingerprints, and it was sufficiently exhaustive enough to represent the structures of the natural products commercially available. The MS/MS spectra of each metabolite were obtained with different types/brands of ion traps (tandem-in-time) or combinations of mass analyzers (tandem-in-space) at multiple collision energies. All spectra were measured repeatedly in each environment because variations can occur in spectra, even under the same conditions. Moreover, the probability, separability of searching, and transferability of this spectral library were evaluated against those of MS/MS libraries, namely: NIST17 and MoNA.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] CFM-ID 4.0: More Accurate ESI-MS/MS Spectral Prediction and Compound Identification
    Wang, Fei
    Liigand, Jaanus
    Tian, Siyang
    Arndt, David
    Greiner, Russell
    Wishart, David S.
    ANALYTICAL CHEMISTRY, 2021, 93 (34) : 11692 - 11700
  • [32] Fact or artifact: the representativeness of ESI-MS for complex natural organic mixtures
    Novotny, Nicole R.
    Capley, Erin N.
    Stenson, Alexandra C.
    JOURNAL OF MASS SPECTROMETRY, 2014, 49 (04): : 316 - 326
  • [33] Low molecular weight organic compounds in atmospheric fine particles by ESI-MS and APPI-MS
    Mazurek, M
    Atkins, PL
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U418 - U418
  • [34] Analysis of 10B antitumoral compounds by means of flow-injection into ESI-MS/MS
    Basilico, F
    Sauerwein, W
    Pozzi, F
    Wattig, A
    Moss, R
    Mauri, PL
    JOURNAL OF MASS SPECTROMETRY, 2005, 40 (12): : 1546 - 1549
  • [35] Biological activities of phenolic compounds extracted from Amaranthaceae plants and their LC/ESI-MS/MS profiling
    Yasir, Muhammad
    Sultana, Bushra
    Amicucci, Matthew
    JOURNAL OF FUNCTIONAL FOODS, 2016, 26 : 645 - 656
  • [36] Lipidomics approaches for a comprehensive analysis of fatty acids and metabolites by LC/ESI-MS
    Kita, Y
    Kihara, Y
    Shimizu, T
    PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2006, 79 (1-2) : 150 - 151
  • [38] Effects of valproate on acylcarnitines in children with epilepsy using ESI-MS/MS
    Werner, Tamara
    Treiss, Irmgard
    Kohlmueller, Dirk
    Mehlem, Peter
    Teich, Martin
    Longin, Elke
    Gerstner, Thorsten
    Koenig, Stephan A.
    Schulze, Andreas
    EPILEPSIA, 2007, 48 (01) : 72 - 76
  • [39] Fragmentation studies of tetrahydropyridocarbazole derivatives by EI, ESI-MS/MS and FAB
    Romeiro, GA
    Ferreira, VF
    Costa, MD
    Joaquim, AM
    Carneiro, JWD
    Kammerer, B
    SPECTROSCOPY-AN INTERNATIONAL JOURNAL, 2001, 15 (01): : 19 - 25
  • [40] Application of direct-infusion ESI-MS/MS for toxicological screening
    Versace, Francois
    Deglon, Julien
    Mangin, Patrice
    Staub, Christian
    BIOANALYSIS, 2014, 6 (15) : 2043 - 2055