Discrimination and classification of ginsenosides and ginsengs using bis-boronic acid receptors in dynamic multicomponent indicator displacement sensor arrays.

Ginsenosides are complex natural products with a diverse array of biological activities, but their molecular recognition and sensing is challenging. A library of simple bis-boronic acid-based receptors with various spacers was synthesized for the sensing of ginsenosides. The incorporation of two boronic acids allowed the pairing of two indicators, which can simultaneously bind the receptors or two saccharides within the ginsenosides. A cross-reactive sensing array was therefore constructed using the receptors in conjunction with different pairs of indicators. LDA plots created from the colorimetric response of the hosts and indicator pairs reveal excellent classification of the ginsenosides, and the corresponding loading plots reveal the cross-reactivity of the receptors. In addition, several commercial ginseng extracts were unambiguously classified using the same sensing array. The assay reported here should be applicable to the analysis of other large saccharide-based natural products.

[1]  Khaled Radad,et al.  Use of ginseng in medicine with emphasis on neurodegenerative disorders. , 2006, Journal of pharmacological sciences.

[2]  Jian Yong Wu,et al.  Development and application of medicinal plant tissue cultures for production of drugs and herbal medicinals in China. , 2006, Natural product reports.

[3]  C. W. Gray,et al.  Boronic acid receptors for alpha-hydroxycarboxylates: high affinity of Shinkai's glucose receptor for tartrate. , 2002, The Journal of organic chemistry.

[4]  S. Shinkai,et al.  Chiral discrimination of monosaccharides using a fluorescent molecular sensor , 1995, Nature.

[5]  V. Lynch,et al.  Colorimetric enantiodiscrimination of α-amino acids in protic media , 2005 .

[6]  E. Anslyn,et al.  A competition assay for determining glucose-6-phosphate concentration with a tris-boronic acid receptor , 1999 .

[7]  J. Sessler,et al.  Boronic acid porphyrin receptor for ginsenoside sensing. , 2010, Organic letters.

[8]  E. Anslyn Supramolecular analytical chemistry. , 2007, The Journal of organic chemistry.

[9]  Eric V. Anslyn,et al.  Indicator-displacement assays , 2006 .

[10]  Philip A. Gale,et al.  Anion Recognition and Sensing: The State of the Art and Future Perspectives. , 2001, Angewandte Chemie.

[11]  Leo A. Joyce,et al.  Pattern-based recognition for the rapid determination of identity, concentration, and enantiomeric excess of subtly different threo diols. , 2009, Journal of the American Chemical Society.

[12]  S. Shinkai,et al.  Discrimination between glucose-1-phosphate and glucose-6-phosphate with a boronic-acid-appended metalloporphyrin , 1995 .

[13]  C. W. Gray,et al.  Boronate derivatives of bioactive amines: potential neutral receptors for anionic oligosaccharides , 2003 .

[14]  Jianzhang Zhao,et al.  Chiral binol-bisboronic acid as fluorescence sensor for sugar acids. , 2004, Angewandte Chemie.

[15]  Wei Wang,et al.  Boronic Acid-Based Sensors , 2002 .

[16]  V. Lynch,et al.  Using enantioselective indicator displacement assays to determine the enantiomeric excess of alpha-amino acids. , 2008, Journal of the American Chemical Society.

[17]  E. Anslyn,et al.  A colorimetric sensing ensemble for heparin. , 2002, Journal of the American Chemical Society.

[18]  Eric V Anslyn,et al.  A general protocol for creating high-throughput screening assays for reaction yield and enantiomeric excess applied to hydrobenzoin , 2009, Proceedings of the National Academy of Sciences.

[19]  Lei Zhu,et al.  Facile quantification of enantiomeric excess and concentration with indicator-displacement assays: an example in the analyses of alpha-hydroxyacids. , 2004, Journal of the American Chemical Society.

[20]  Juyoung Yoon,et al.  New fluorescent and colorimetric chemosensors based on the rhodamine and boronic acid groups for the detection of Hg2 , 2010 .

[21]  A. Schiller,et al.  Recognition of phospho sugars and nucleotides with an array of boronic acid appended bipyridinium salts. , 2008, Analytica chimica acta.

[22]  Eric V Anslyn,et al.  Threshold detection using indicator-displacement assays: an application in the analysis of malate in Pinot Noir grapes. , 2004, Journal of the American Chemical Society.

[23]  Félix Sancenón,et al.  Fluorogenic and chromogenic chemosensors and reagents for anions. , 2003, Chemical reviews.

[24]  E. Anslyn,et al.  A functional assay for heparin in serum using a designed synthetic receptor. , 2005, Angewandte Chemie.

[25]  E. Anslyn,et al.  A colorimetric boronic acid based sensing ensemble for carboxy and phospho sugars. , 2006, Organic letters.

[26]  K. Severin,et al.  Easy to optimize: dynamic combinatorial libraries of metal-dye complexes as flexible sensors for tripeptides. , 2006, Journal of combinatorial chemistry.

[27]  Jianzhang Zhao,et al.  An enantioselective fluorescent sensor for sugar acids. , 2004, Journal of the American Chemical Society.

[28]  V. Lynch,et al.  A structural investigation of the N-B interaction in an o-(N,N-dialkylaminomethyl)arylboronate system. , 2006, Journal of the American Chemical Society.

[29]  Karl J. Wallace,et al.  Slow anion exchange, conformational equilibria, and fluorescent sensing in venus flytrap aminopyridinium-based anion hosts. , 2003, Journal of the American Chemical Society.

[30]  J. McDevitt,et al.  A multicomponent sensing ensemble in solution: differentiation between structurally similar analytes. , 2003, Angewandte Chemie.

[31]  Gail Gong Cross-Validation, the Jackknife, and the Bootstrap: Excess Error Estimation in Forward Logistic Regression , 1986 .

[32]  John J. Lavigne,et al.  Neue Tricks für alte Indikatoren: ein colorimetrisches Chemosensor-Ensemble für Tartrat/Malat in Getränken , 1999 .

[33]  Jianzhang Zhao,et al.  Chiral donor photoinduced-electron-transfer (d-PET) boronic acid chemosensors for the selective recognition of tartaric acids, disaccharides, and ginsenosides. , 2011, Chemistry.

[34]  Paul M. Levine,et al.  Boronic acid-appended bis-viologens as a new family of viologen quenchers for glucose sensing , 2008 .

[35]  Francis L Martin,et al.  Derivation of a subtype-specific biochemical signature of endometrial carcinoma using synchrotron-based Fourier-transform infrared microspectroscopy. , 2009, Cancer letters.

[36]  T. Schrader,et al.  A color sensor for catecholamines. , 2005, Angewandte Chemie.

[37]  E. Anslyn,et al.  Teaching old indicators new tricks. , 2001, Accounts of chemical research.

[38]  N. Fuzzati Analysis methods of ginsenosides. , 2004, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[39]  Kay Severin,et al.  Pattern-based sensing with metal-dye complexes: sensor arrays versus dynamic combinatorial libraries. , 2010, Journal of combinatorial chemistry.

[40]  E. Anslyn,et al.  Teaching Old Indicators New Tricks: A Colorimetric Chemosensing Ensemble for Tartrate/Malate in Beverages. , 1999, Angewandte Chemie.

[41]  K. Niikura,et al.  CHEMOSENSOR ENSEMBLE WITH SELECTIVITY FOR INOSITOL-TRISPHOSPHATE , 1998 .

[42]  Philip A. Gale,et al.  Erkennung und Nachweis von Anionen: gegenwärtiger Stand und Perspektiven , 2001 .

[43]  Hildegarde Heymann,et al.  Discrimination of flavonoids and red wine varietals by arrays of differential peptidic sensors , 2011 .

[44]  Bisoxazolidine-catalyzed enantioselective alkynylation of aldehydes. , 2006, Journal of the American Chemical Society.

[45]  Binghe Wang,et al.  Progress in Boronic Acid-Based Fluorescent Glucose Sensors , 2004, Journal of Fluorescence.

[46]  Lei Zhu,et al.  Guidelines in implementing enantioselective indicator-displacement assays for alpha-hydroxycarboxylates and diols. , 2005, Journal of the American Chemical Society.

[47]  M. Adams,et al.  Differential sensing using proteins: exploiting the cross-reactivity of serum albumin to pattern individual terpenes and terpenes in perfume. , 2009, Journal of the American Chemical Society.

[48]  E. Anslyn,et al.  Using a synthetic receptor to create an optical-sensing ensemble for a class of analytes: a colorimetric assay for the aging of scotch. , 2001, Journal of the American Chemical Society.

[49]  Byron E. Collins,et al.  Probing intramolecular B-N interactions in ortho-aminomethyl arylboronic acids. , 2009, The Journal of organic chemistry.

[50]  A. W. Czarnik,et al.  Desperately seeking sensors. , 1995, Chemistry & biology.

[51]  V. Lynch,et al.  Thermodynamic analysis of receptors based on guanidinium/boronic acid groups for the complexation of carboxylates, alpha-hydroxycarboxylates, and diols: driving force for binding and cooperativity. , 2004, Chemistry.

[52]  H. Matsuda,et al.  Chemical constituents from seeds of Panax ginseng: structure of new dammarane-type triterpene ketone, panaxadione, and hplc comparisons of seeds and flesh. , 2009, Chemical & pharmaceutical bulletin.

[53]  M. Cacciarini,et al.  A new tripodal receptor for molecular recognition of monosaccharides. A paradigm for assessing glycoside binding affinities and selectivities by 1H NMR spectroscopy. , 2004, Journal of the American Chemical Society.

[54]  F. Schmidtchen,et al.  Artificial Organic Host Molecules for Anions. , 1997, Chemical reviews.

[55]  K. Bae,et al.  Ginsenosides from heat processed ginseng. , 2009, Chemical & pharmaceutical bulletin.

[56]  P. But,et al.  Differentiation and authentication of Panax ginseng, Panax quinquefolius, and ginseng products by using HPLC/MS. , 2000, Analytical chemistry.

[57]  Gregory A. Bakken,et al.  Computational methods for the analysis of chemical sensor array data from volatile analytes. , 2000, Chemical reviews.

[58]  Yu Yang,et al.  Luminescent Open Metal Sites within a Metal–Organic Framework for Sensing Small Molecules , 2007 .

[59]  Minyong Li,et al.  Synthesis and carbohydrate binding studies of fluorescent alpha-amidoboronic acids and the corresponding bisboronic acids. , 2010, Bioorganic & medicinal chemistry.

[60]  K. Severin,et al.  Sensing of peptide hormones with dynamic combinatorial libraries of metal-dye complexes: the advantage of time-resolved measurements. , 2009, Organic & biomolecular chemistry.

[61]  A. P. Silva,et al.  Newer optical-based molecular devices from older coordination chemistry , 2003 .