Methods for the differential integrative Omic analysis of plasma from a transgenic disease animal model

Eugene Davidov; Clary B. Clish; Matej Orešič; Michael Meys; Wayne Stochaj; Philip Snell; Gary Lavine; Thomas R. Londo; Aram Adourian; Xian Zhang; Mark Johnston; Nicole Morel; Edward W. Marple; Thomas N. Plasterer; Eric Neumann; Elwin Verheij; Jack T.W.E. Vogels; Louis M. Havekes; Jan Van Der Greef; Stephen Naylor

doi:10.1089/omi.2004.8.267

Methods for the differential integrative Omic analysis of plasma from a transgenic disease animal model

Eugene Davidov, Clary B. Clish, Matej Orešič, Michael Meys, Wayne Stochaj, Philip Snell, Gary Lavine, Thomas R. Londo, Aram Adourian, Xian Zhang, Mark Johnston, Nicole Morel, Edward W. Marple, Thomas N. Plasterer, Eric Neumann, Elwin Verheij, Jack T.W.E. Vogels, Louis M. Havekes, Jan Van Der Greef, Stephen Naylor

VTT Technical Research Centre of Finland

Research output: Contribution to journal › Article › Scientific › peer-review

36 Citations (Scopus)

Abstract

Multitiered quantitative analysis of biological systems is rapidly becoming the desired approach to study hierarchical functional interactions between proteins and metabolites. We describe here a novel systematic approach to analyze organisms with complex metabolic regulatory networks. By using precise analytical methods to measure biochemical constituents and their relative abundance in whole plasma of transgenic ApoE*3-Leiden mice and an isogenic wild-type control group, simultaneous snapshots of metabolic and protein states were obtained. Novel data processing and multivariate analysis tools such as Impurity Resolution Software (IMPRESS™) and Windows-based linear fit program (WINLIN™) were used to compare protein and metabolic profiles in parallel. Canonical correlations of the resulting data show quantitative relationships between heterogeneous components in the TG animals. These results, obtained solely from whole plasma analysis allowed us, in a rapid manner, to corroborate previous findings as well as find new events pertaining to dominant and peripheral events in lipoprotein metabolism of a genetically modified mammalian organism in relation to ApoE3, a key mediator of lipoprotein metabolism.

Original language	English
Pages (from-to)	267-288
Journal	OMICS: A Journal of Integrative Biology
Volume	8
Issue number	4
DOIs	https://doi.org/10.1089/omi.2004.8.267
Publication status	Published - 2004
MoE publication type	A1 Journal article-refereed

Access to Document

10.1089/omi.2004.8.267

Cite this

Davidov, E., Clish, C. B., Orešič, M., Meys, M., Stochaj, W., Snell, P., Lavine, G., Londo, T. R., Adourian, A., Zhang, X., Johnston, M., Morel, N., Marple, E. W., Plasterer, T. N., Neumann, E., Verheij, E., Vogels, J. T. W. E., Havekes, L. M., Van Der Greef, J., & Naylor, S. (2004). Methods for the differential integrative Omic analysis of plasma from a transgenic disease animal model. OMICS: A Journal of Integrative Biology, 8(4), 267-288. https://doi.org/10.1089/omi.2004.8.267

@article{d2b25dbdc3574f00acd497747d53bf89,

title = "Methods for the differential integrative Omic analysis of plasma from a transgenic disease animal model",

abstract = "Multitiered quantitative analysis of biological systems is rapidly becoming the desired approach to study hierarchical functional interactions between proteins and metabolites. We describe here a novel systematic approach to analyze organisms with complex metabolic regulatory networks. By using precise analytical methods to measure biochemical constituents and their relative abundance in whole plasma of transgenic ApoE*3-Leiden mice and an isogenic wild-type control group, simultaneous snapshots of metabolic and protein states were obtained. Novel data processing and multivariate analysis tools such as Impurity Resolution Software (IMPRESS{\texttrademark}) and Windows-based linear fit program (WINLIN{\texttrademark}) were used to compare protein and metabolic profiles in parallel. Canonical correlations of the resulting data show quantitative relationships between heterogeneous components in the TG animals. These results, obtained solely from whole plasma analysis allowed us, in a rapid manner, to corroborate previous findings as well as find new events pertaining to dominant and peripheral events in lipoprotein metabolism of a genetically modified mammalian organism in relation to ApoE3, a key mediator of lipoprotein metabolism.",

author = "Eugene Davidov and Clish, {Clary B.} and Matej Ore{\v s}i{\v c} and Michael Meys and Wayne Stochaj and Philip Snell and Gary Lavine and Londo, {Thomas R.} and Aram Adourian and Xian Zhang and Mark Johnston and Nicole Morel and Marple, {Edward W.} and Plasterer, {Thomas N.} and Eric Neumann and Elwin Verheij and Vogels, {Jack T.W.E.} and Havekes, {Louis M.} and {Van Der Greef}, Jan and Stephen Naylor",

year = "2004",

doi = "10.1089/omi.2004.8.267",

language = "English",

volume = "8",

pages = "267--288",

journal = "OMICS: A Journal of Integrative Biology",

issn = "1536-2310",

publisher = "Mary Ann Liebert",

number = "4",

}

Davidov, E, Clish, CB, Orešič, M, Meys, M, Stochaj, W, Snell, P, Lavine, G, Londo, TR, Adourian, A, Zhang, X, Johnston, M, Morel, N, Marple, EW, Plasterer, TN, Neumann, E, Verheij, E, Vogels, JTWE, Havekes, LM, Van Der Greef, J & Naylor, S 2004, 'Methods for the differential integrative Omic analysis of plasma from a transgenic disease animal model', OMICS: A Journal of Integrative Biology, vol. 8, no. 4, pp. 267-288. https://doi.org/10.1089/omi.2004.8.267

TY - JOUR

T1 - Methods for the differential integrative Omic analysis of plasma from a transgenic disease animal model

AU - Davidov, Eugene

AU - Clish, Clary B.

AU - Orešič, Matej

AU - Meys, Michael

AU - Stochaj, Wayne

AU - Snell, Philip

AU - Lavine, Gary

AU - Londo, Thomas R.

AU - Adourian, Aram

AU - Zhang, Xian

AU - Johnston, Mark

AU - Morel, Nicole

AU - Marple, Edward W.

AU - Plasterer, Thomas N.

AU - Neumann, Eric

AU - Verheij, Elwin

AU - Vogels, Jack T.W.E.

AU - Havekes, Louis M.

AU - Van Der Greef, Jan

AU - Naylor, Stephen

PY - 2004

Y1 - 2004

N2 - Multitiered quantitative analysis of biological systems is rapidly becoming the desired approach to study hierarchical functional interactions between proteins and metabolites. We describe here a novel systematic approach to analyze organisms with complex metabolic regulatory networks. By using precise analytical methods to measure biochemical constituents and their relative abundance in whole plasma of transgenic ApoE*3-Leiden mice and an isogenic wild-type control group, simultaneous snapshots of metabolic and protein states were obtained. Novel data processing and multivariate analysis tools such as Impurity Resolution Software (IMPRESS™) and Windows-based linear fit program (WINLIN™) were used to compare protein and metabolic profiles in parallel. Canonical correlations of the resulting data show quantitative relationships between heterogeneous components in the TG animals. These results, obtained solely from whole plasma analysis allowed us, in a rapid manner, to corroborate previous findings as well as find new events pertaining to dominant and peripheral events in lipoprotein metabolism of a genetically modified mammalian organism in relation to ApoE3, a key mediator of lipoprotein metabolism.

AB - Multitiered quantitative analysis of biological systems is rapidly becoming the desired approach to study hierarchical functional interactions between proteins and metabolites. We describe here a novel systematic approach to analyze organisms with complex metabolic regulatory networks. By using precise analytical methods to measure biochemical constituents and their relative abundance in whole plasma of transgenic ApoE*3-Leiden mice and an isogenic wild-type control group, simultaneous snapshots of metabolic and protein states were obtained. Novel data processing and multivariate analysis tools such as Impurity Resolution Software (IMPRESS™) and Windows-based linear fit program (WINLIN™) were used to compare protein and metabolic profiles in parallel. Canonical correlations of the resulting data show quantitative relationships between heterogeneous components in the TG animals. These results, obtained solely from whole plasma analysis allowed us, in a rapid manner, to corroborate previous findings as well as find new events pertaining to dominant and peripheral events in lipoprotein metabolism of a genetically modified mammalian organism in relation to ApoE3, a key mediator of lipoprotein metabolism.

U2 - 10.1089/omi.2004.8.267

DO - 10.1089/omi.2004.8.267

M3 - Article

SN - 1536-2310

VL - 8

SP - 267

EP - 288

JO - OMICS: A Journal of Integrative Biology

JF - OMICS: A Journal of Integrative Biology

IS - 4

ER -

Methods for the differential integrative Omic analysis of plasma from a transgenic disease animal model

Abstract

Access to Document

Fingerprint

Cite this