BindPro ™ Metabolomics Allows For Enrichment of Metabolites/Analytes By Removing Proteins From Serum or Plasma For Metabolomics Research.

BindPro ™ Metabolomics Allows For Enrichment of Metabolites/Analytes By Removing Proteins From Serum or Plasma For Metabolomics Research.

BindPro ™ Metabolomics Allows For Enrichment of Metabolites/Analytes By Removing Proteins From Serum or Plasma For Metabolomics Research.

For the determination of metabolites from human serum and plasma, sample preparation is necessary before metabolites/analytes are detected by MS/GC/LC/NMR. Because proteins interfere with metabolite/analytes analysis, it is important to remove proteins and enrich metabolites/analytes using BindPro™ Metabolomics. BindPro™ Metabolomics has higher efficiency compared to other methods like chemical precipitation or membrane filtration because BindPro™ Metabolomics lacks the disadvantages of cross contamination and shear damage. It is ideal for analytes that are water soluble. Consequently, BindPro™ Metabolomics has applications in a range of drug binding, screening(toxicology, transplant monitoring) and metabolomic research (protein-metabolite interactions, biomarker discovery, and functional annotation of both proteins and metabolites).

BindPro™ Metabolomics allows you to enrich metabolites or analytes by removing proteins from the serum or plasma samples. After using BindPro™ Metabolomics, the analysis of metabolite/analyte data profiles using MS/GC/LC/NMR is beneficial for understanding the close biological associations of metabolites/analytes. Some examples of metabolites/analytes present in biological samples are sodium, sulfur, magnesium, phosphorus, phosphates, potassium, iron, oxygen, bicarbonate, L-alanine, carbon dioxide, chlorine, L-lysine, fructosamine, calcium, urea, melanin, D-glucose, total cholesterol, ATP, glyceraldehyde , cholesterol esters, methanol, glycine, uric acid, and (R)-3-hydroxybutyric acid.

Research publications have shown that serum and plasma samples are ideal for metabolomics research. After using BindPro™ Metabolomics for protein removal, serum and plasma samples are compatible for downstream applications such as MS/GC/LC/NMR that enable metabolomics research. BindPro™ Metabolomics has an efficacious extraction technique for performing large-scale, highthroughput protein removal from serum or plasma samples.

Published Articles for BindPro™

Wolbachia Lipoprotein Stimulates Innate and Adaptive Immunity through Toll-like Receptors 2 and 6 to Induce Disease Manifestations of Filariasis

BindPro™ can eliminate the artifacts of protein contamination and improve study of amino acids, sugars, lipids, nucleotides, and other biomolecules from biological tissues and fluids. In this article, researchers used Cleanascite™ first to determine if TLR2/6 ligands of Wolbachia are lipoproteins for removing lipids and lipoproteins. Next BindPro™, a polymeric protein removal suspension reagent (Biotech Support Group)was used to ablate levels of HEK-TLR2 cell IL-8 reporter gene activity to BMFE thereby showing that the TLR2/6 activity depends on both lipid and protein moieties.

For more information: http://biotechsupportgroup.com/bindpro
Applications of BindPro™: http://biotechsupportgroup.com/applications/bindpro%E2%84%A2-applications

References for BindPro™:

  1. Wolbachia Lipoprotein Stimulates Innate and Adaptive Immunity through Toll-like Receptors 2 and 6 to Induce Disease Manifestations of Filariasis Joseph D. Turner J. Biol. Chem. 2009 284: 22364-22378.
  2. Metabolomics Research References:

  3. K. Dettmer, P.A. Aronov and B.D. Hammock, Mass spectrometry-based metabolomics, Mass Spectrom Rev 26 (2007), 51–78.
  4. Lawton KA, Berger A, Mitchell M, Milgram KE, Evans AM, et al. (2008) Analysis of the adult human plasma metabolome. Pharmacogenomics 9: 383–397.
  5. R. Breitling, A.R. Pitt and M.P. Barrett, Precision mapping of the metabolome, Trends Biotechnol 24 (2006), 543–548.
  6. R Rosewell and C Vitols. March 2006. Identifying Metabolites in Biofluids. Chenomx Inc.
  7. D Chang, J Newton, C Vitols, and AM Weljie. Identifying and Quantifying Metabolites in Blood Serum and Plasma. Chenomx Inc.
  8. Hollywood K, Brison DR, Goodacre R (2006) Metabolomics: Current technologies and future trends. Proteomics 6: 4716–4723.
  9. LH Lucas, CK Larive, PS Wilkinson, and S Huhn. Progress toward automated metabolic profiling of human serum: Comparison of CPMG and gradient-filtered NMR analytical methods. J Pharm Biomed Anal. 2005 39(1-2):156-163
  10. Fiehn, O. 2002. Metabolomics—the link between genotypes and phenotypes. Plant Mol. Biol. 48:155-171. 5. 2.) Nielsen, J., and S. Oliver. 2005.
  11. The next wave in metabolome analysis. Trends Biotechnol. 2005. 23:544-546. 6.
  12. Villas-Boas, S.G., J. Hojer-Pedersen, M. Akesson, J. Smedsgaard, and J. Nielsen. 2005. Global metabolite analysis of yeast: evaluation of sample preparation methods. Yeast 22:1155-1169.
  13. Soga, T., Y. Ohashi, Y. Ueno, H. Naraoka, M. Tomita, and T. Nishioka. 2003. Quantitative metabolome analysis using capillary electrophoresis mass spectrometry. J. Proteome Res. 2:488-494. 9.
  14. C.A. Daykin, P.J.D. Foxall, S.C. Connor, J.C. Lindon and J.K. Nicholson, The comparison of plasma deproteinization methods for the detection of low-molecular-weight metabolites by 1 H nuclear magnetic resonance spectroscopy, Anal Biochem304 (2002), 220–230.
  15. CA Daykin, PJ Foxall, SC Connor, JC Lindon, and JK Nicholson. 2002. The comparison of plasma deproteinization methods for the detection of low-molecular-weight metabolites by 1H nuclear magnetic resonance spectroscopy. Anal Biochem. 2002. 304(2):220-230
  16. Fiehn, O., J. Kopka, P. Dörmann, T. Altmann, R.N. Trethewey, and L. Willmitzer. Metabolite profiling for plant functional genomics. Nat. Biotechnol. 2000. 18:1157-1161.
  17. Plumb, R.S., C.L. Stumpf, M.V. Gorenstein, J.M. Castro-Perez, G.J. Dear, M. Anthony, B.C. Sweatman, S.C. Connor, and J.N. Haselden. 2002. Metabonomics: the use of electrospray mass spectrometry coupled to reversed-phase liquid chromatography shows potential for the screening of rat urine in drug development. Rapid Commun. Mass Spectrom. 16:1991-1996.

Comments