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  7. Topics
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We are analyzing https://link.springer.com/protocol/10.1007/978-1-60761-322-0_22.

Title:
Comprehensive Quantitative Analysis of Bioactive Sphingolipids by High-Performance Liquid Chromatography–Tandem Mass Spectrometry | SpringerLink
Description:
There has been a recent explosion in research concerning novel bioactive sphingolipids (SPLs) such as ceramide (Cer), sphingosine (Sph), and sphingosine 1-phosphate (Sph-1P) and this has necessitated the development of accurate and user-friendly methodology for...
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Education
  • Health & Fitness

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We don’t know how the website earns money.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

google, scholar, cas, mass, article, spectrometry, analysis, pubmed, sphingolipids, liquid, molecular, ceramide, method, lipid, quantitative, bioactive, chem, anal, biochem, content, highperformance, ceramides, ionization, biol, spectrom, privacy, cookies, information, publish, protocol, chromatographytandem, bielawska, methods, metabolism, cell, adams, determination, tandem, merrill, species, sphingomyelin, chromatography, research, search, lipidomics, bielawski, szulc, spls, sphingosine, simultaneous,

Topics {✒️}

maldi-qit-tof mass spectrometry maldi-ion momility-tof ms simultaneous esi/ms/ms analysis lc-ms/ms multiplexed method structure-specific collision-induced fragmentation lc/ms/ms system tandem mass spectrometry gas liquid chromatography obese insulin-resistant humans esi/ms/ms methodology maldi-ion mobility-tofms lipid/peptide/nucleotide separation springer science+business media lipid-mediated cell regulation comprehensive quantitative analysis simultaneous quantitative analysis lc–ms/ms esi-ms/ms privacy choices/manage cookies positive ionization mode collision-induced decomposition mass spectrometry lipidomics shared resource parent ion scan transcriptional activation induced author information authors collision gas flow human cerebrospinal fluid human alveolar macrophages solid-phase extraction phospholipid molecular species european economic area user-friendly methodology peak area ratios linear regression model robust analytical procedure cooperative prosurvival activity acid ceramidase activity generating death signals phosphatidylcholine-specific phospholipase complex lipid mixtures direct tissue analysis convenient structural analysis journal finder publish conditions privacy policy sphingomyelin synthase account diglyceride kinase assay protocol bielawski ceramide-centric universe eukaryotic cell signaling

Questions {❓}

  • , (1998) Sphingomyelin synthase, a potential regulator of intracellular levels of ceramide and diacylglycerol during SV40 transformation – Does sphingomyelin synthase account for the putative, phosphatidylcholine-specific phospholipase C?

Schema {🗺️}

ScholarlyArticle:
      headline:Comprehensive Quantitative Analysis of Bioactive Sphingolipids by High-Performance Liquid Chromatography–Tandem Mass Spectrometry
      pageEnd:467
      pageStart:443
      image:https://media.springernature.com/w153/springer-static/cover/book/978-1-60761-322-0.jpg
      genre:
         Springer Protocols
      isPartOf:
         name:Lipidomics
         isbn:
            978-1-60761-322-0
            978-1-60761-321-3
         type:Book
      publisher:
         name:Humana Press
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Jacek Bielawski
            affiliation:
                  name:Medical University of South Carolina
                  address:
                     name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jason S. Pierce
            affiliation:
                  name:Medical University of South Carolina
                  address:
                     name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Justin Snider
            affiliation:
                  name:Medical University of South Carolina
                  address:
                     name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Barbara Rembiesa
            affiliation:
                  name:Medical University of South Carolina
                  address:
                     name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Zdzislaw M. Szulc
            affiliation:
                  name:Medical University of South Carolina
                  address:
                     name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Alicja Bielawska
            affiliation:
                  name:Medical University of South Carolina
                  address:
                     name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
      keywords:Endogenous sphingolipid, Ceramide, Dihydroceramide, Sphingoid base, Sphingoid base phosphate, Sphingosine, Sphingosine 1-phosphate, Sphingomyelin, HPLC–MS analysis, ESI/MS/MS analysis
      description:There has been a recent explosion in research concerning novel bioactive sphingolipids (SPLs) such as ceramide (Cer), sphingosine (Sph), and sphingosine 1-phosphate (Sph-1P) and this has necessitated the development of accurate and user-friendly methodology for analyzing and quantitating the endogenous levels of these molecules. ESI/MS/MS methodology provides a universal tool used for detecting and monitoring changes in SPL levels and composition from biological materials. Simultaneous ESI/MS/MS analysis of sphingoid bases (SBs), sphingoid base 1-phosphates (SB-1Ps), ceramides (Cers), ceramide 1-phosphates (Cer-1P), glucosyl/galactosyl-ceramides (Glu-Cers), and sphingomyelins (SMs) is performed on a Thermo Fisher Scientific triple quadrupole mass spectrometer operating in a multiple reaction monitoring (MRM) positive ionization mode. Biological materials (cells, tissues, or physiological fluids) are fortified with internal standards (ISs), extracted into a one-phase neutral organic solvent system, and analyzed by a LC/MS/MS system. Qualitative analysis (identification) of SPLs is performed by a Parent Ion scan of a common fragment ion characteristic for a particular class of SPLs. Quantitative analysis is based on calibration curves generated by spiking an artificial matrix with known amounts of target analyte, synthetic standards, and an equal amount of IS. The calibration curves are constructed by plotting the peak area ratios of analyte to the respective IS against concentration, using a linear regression model. This robust analytical procedure can determine the composition of endogenous sphingolipids (ESPLs) in varied biological materials and achieve a detection limit of subpicomole level. This methodology constitutes a “Lipidomic” approach to study the SPLs metabolism, defining a function of distinct subspecies of individual bioactive SPL classes.
      datePublished:2009
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Book:
      name:Lipidomics
      isbn:
         978-1-60761-322-0
         978-1-60761-321-3
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      name:Humana Press
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Medical University of South Carolina
      address:
         name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
         type:PostalAddress
      name:Medical University of South Carolina
      address:
         name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
         type:PostalAddress
      name:Medical University of South Carolina
      address:
         name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
         type:PostalAddress
      name:Medical University of South Carolina
      address:
         name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
         type:PostalAddress
      name:Medical University of South Carolina
      address:
         name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
         type:PostalAddress
      name:Medical University of South Carolina
      address:
         name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
         type:PostalAddress
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      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Jacek Bielawski
      affiliation:
            name:Medical University of South Carolina
            address:
               name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
               type:PostalAddress
            type:Organization
      name:Jason S. Pierce
      affiliation:
            name:Medical University of South Carolina
            address:
               name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
               type:PostalAddress
            type:Organization
      name:Justin Snider
      affiliation:
            name:Medical University of South Carolina
            address:
               name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
               type:PostalAddress
            type:Organization
      name:Barbara Rembiesa
      affiliation:
            name:Medical University of South Carolina
            address:
               name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
               type:PostalAddress
            type:Organization
      name:Zdzislaw M. Szulc
      affiliation:
            name:Medical University of South Carolina
            address:
               name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
               type:PostalAddress
            type:Organization
      name:Alicja Bielawska
      affiliation:
            name:Medical University of South Carolina
            address:
               name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
      name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
      name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
      name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
      name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
      name:Department of Biochemistry and Molecular Biology, Lipidomic Core Mass Spectrometry Lab, Medical University of South Carolina, Charleston, USA
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External Links {🔗}(110)

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