Plasmalogen Analysis Service

Plasmalogens (ether phospholipids) are central to membrane dynamics, redox balance, and metabolism—but vinyl-ether bonds complicate quantification. Creative Proteomics offers high-resolution LC–MS/MS profiling with GC–MS verification to accurately distinguish plasmalogens (P-) from plasmanyl (O-) species across complex matrices.

  • Resolve isobaric ether lipids; clear P- vs O- differentiation
  • Redox-stabilized extraction to preserve vinyl-ether integrity
  • HRAM Orbitrap + Triple Quad for discovery and targeted quantification
  • GC–MS DMA confirmation for bond-type validation
  • Sensitive detection of low-abundance species with reproducible results

Tell us your matrix and goals—we'll configure a P-/O-selective workflow and hand you clean, comparable data.

Request Analysis

Submit Your Request Now

×
Boston University
University at Buffalo
UMass Medical School
Hawaii Pacific University
Medizinische Fakultät
Louisiana State University
Nyulangone
Nature's Fynd
Dietary Supplement Manufacturer
  • Solution We Provide
  • Detectable Species
  • Advantages
  • Workflow
  • Methods
  • Results and Data Analysis
  • Sample Requirements
  • FAQ

What Is Plasmalogen?

Plasmalogens are a specialized subclass of glycerophospholipids characterized by a vinyl-ether linkage at the sn-1 position and an esterified fatty acid at sn-2. They are most commonly found as phosphatidylethanolamine (PE[P-]) and phosphatidylcholine (PC[P-]) species in cellular membranes.

This vinyl-ether bond gives plasmalogens unique biochemical properties. It enhances membrane fluidity, contributes to lipid raft formation, and provides antioxidant capacity by scavenging reactive oxygen species. These functions make plasmalogens particularly relevant in studies of oxidative stress, aging, neurobiology, and lipid remodeling.

Analytically, distinguishing between plasmalogens (P-) and plasmanyl lipids (O-) is essential. Although isobaric, only plasmalogens contain the vinyl-ether bond, which requires bond-specific confirmation to avoid misidentification. As such, targeted workflows that preserve the vinyl linkage and separate isomeric species are critical for accurate measurement.

Plasmalogen Analysis Solutions at Creative Proteomics

Targeted Plasmalogen Quantification (PE[P-], PC[P-])

Quantify predefined plasmalogen species using internal standards and matrix-matched calibration. Scheduled MRM/PRM ensures reproducible absolute or relative results.

Comprehensive Ether Lipid Profiling

Profile both plasmalogens (P-) and plasmanyl (O-) lipids to reveal the balance between vinyl-ether and alkyl-ether forms in your samples.

Vinyl-Ether Bond Confirmation (Optional)

Confirm true plasmalogens via acid cleavage and GC–MS detection of dimethyl acetals (DMA), resolving isobaric O-ether interferences.

Isomer-Resolved Annotation

High-resolution LC–MS/MS distinguishes positional and structural isomers sharing the same m/z, improving annotation confidence.

Redox-Protected Extraction

Cold, antioxidant-assisted extraction prevents vinyl-ether oxidation and maintains molecular integrity throughout processing.

Custom Analytical Panel Design

Tailor compound panels by headgroup, chain length, or unsaturation level to match specific research or metabolic applications.

Complete List of Detectable Plasmalogen Species

ClassValidated species (sum composition examples)
PE-plasmalogens (PE[P-])PE(P-16:0/18:1), PE(P-16:0/18:2), PE(P-16:0/20:4), PE(P-16:0/22:6), PE(P-18:0/18:1), PE(P-18:0/18:2), PE(P-18:0/20:4), PE(P-18:0/22:6), PE(P-18:1/18:1), PE(P-18:1/20:4)
PC-plasmalogens (PC[P-])PC(P-16:0/18:1), PC(P-16:0/18:2), PC(P-16:0/20:4), PC(P-16:0/22:6), PC(P-18:0/18:1), PC(P-18:0/20:4), PC(P-18:0/22:6), PC(P-18:1/20:4)
Lyso-plasmalogens (LPE[P-], LPC[P-])LPE(P-16:0/0:0), LPE(P-18:0/0:0), LPE(P-18:1/0:0); LPC(P-16:0/0:0), LPC(P-18:0/0:0), LPC(P-18:1/0:0)
Plasmanyl ether PE (PE[O-])PE(O-16:0/18:1), PE(O-16:0/20:4), PE(O-16:0/22:6), PE(O-18:0/20:4), PE(O-18:0/22:6)
Plasmanyl ether PC (PC[O-])PC(O-16:0/18:1), PC(O-16:0/20:4), PC(O-16:0/22:6), PC(O-18:0/20:4), PC(O-18:0/22:6)

Notes: Species availability depends on matrix and standards. We confirm plasmenyl (P-) vs plasmanyl (O-) where required. Panel expansion to additional chains (e.g., 22:5, 20:1) is available on request.

Why Choose Our Plasmalogen Assay?

  • Bond-type certainty
    LC–MS/MS annotation paired with optional vinyl-ether cleavage → DMA readout (GC–MS) reduces P- vs O-ether misassignment in challenging matrices.
  • High mass accuracy & resolution
    HRAM platforms deliver ≤3 ppm typical mass error with 60k–120k resolving power at m/z 200, improving separation of isobars and adducts.
  • Targeted sensitivity for low-abundance species
    Scheduled MRM on triple quadrupoles supports sub-ng/mL level quantitation in suitable matrices when matched standards are available.
  • Redox-safe sample handling
    Cold extraction with antioxidants and metal chelators helps preserve vinyl-ether integrity and minimizes artificial oxidation.
  • Quantitative rigor
    Class-matched internal standards, matrix-matched calibration, and calibration fits targeting R2 ≥ 0.995; intra-batch QC typically CV ≤ 20% for well-behaved species.
  • Isomer-aware verification
    Diagnostic fragment ions and retention-time rulesets flag ambiguous calls; uncertain IDs are clearly annotated with confidence notes.
  • Transparent QA package
    Blanks, spikes, pooled QCs, and system-suitability checks are delivered with plots and acceptance criteria for easy review.

How Creative Proteomics Provides Plasmalogen Assay?

Workflow for Plasmalogen Analysis

What Methods are Used for Our Plasmalogen Analysis?

HRAM LC–MS Profiling (untargeted/species-resolved):

Platforms: Thermo Orbitrap Exploris 480 or Q Exactive HF-X

LC: C18 reverse-phase (2.1 × 100 mm, 1.7 µm); gradient of ACN/H₂O and IPA/ACN with ammonium formate/formic acid

Ionization & Scans: ESI±; full scan m/z 200–2,000 with data-dependent MS/MS; resolving power typically 60k–120k at m/z 200

Purpose: Comprehensive coverage for plasmalogen species annotation and isobar resolution

Targeted LC–MS/MS (absolute/relative quant):

Platforms: SCIEX Triple Quad 6500+ or equivalent.

Acquisition: Scheduled MRM of PE(P-) and PC(P-) transitions; class-specific fragments and acyl anions in confirmatory MS/MS.

Purpose: High-sensitivity quant for predefined panels.

Vinyl-Ether Confirmation (optional):

Chemistry: Acid cleavage of the vinyl-ether to form dimethyl acetals (DMAs).

GC–MS: DMA profiling confirms plasmalogen presence alongside LC–MS species calls.

Key QA/Controls: Class-matched internal standards, pooled-matrix QCs, blanks, and replicate injections.

SCIEX Triple Quad™ 6500+

SCIEX Triple Quad™ 6500+ (Figure from Sciex)

Thermo Q Exactive HF-X MS

Q Exactive HF-X MS

Orbitrap Exploris 480

Orbitrap Exploris 480 (Figure from Thermo Fisher)

Plasmalogen Analysis Service: Results and Data Analysis

Standard Deliverables

  • Quantitative Result Tables — Absolute or relative concentrations (e.g., pmol/mg tissue, ng/mL) of detected plasmalogen and related ether lipid species.
  • Lipid Class Summary Reports — Aggregated abundance of PE(P-), PC(P-), and O-ether subclasses with matrix-specific comparisons.
  • Normalized Data Matrices — Internal-standard–corrected data, adjusted for sample loading, and formatted for direct import into statistical tools (e.g., MetaboAnalyst, SIMCA).
  • Full Raw Data Files — Provided in Thermo .raw and open .mzML formats for reanalysis, transparency, or publication submission.
  • Quality Control Reports — Including internal standard recovery, RSD%, blank assessments, and calibration performance summaries.
  • Representative LC–MS/MS Chromatograms — Extracted ion traces and annotated spectra confirming plasmalogen identity and retention consistency.
LC–MS/MS figure showing chromatographic separation of PE(P-16:0/20:4) and PE(O-16:0/20:4) with labeled MS/MS fragment ions confirming plasmalogen structure.

LC–MS/MS Chromatographic & MS/MS Confirmation of Plasmalogens

Dual-panel figure with bar chart of plasmalogen class distribution and volcano plot showing upregulated PE(P-36:1) and PC(P-36:1) species between experimental groups.

Plasmalogen Class Distribution and Differential Analysis

Advanced Data Analysis (Optional)

  • Multivariate Statistics — PCA, PLS-DA, and clustering to explore group separations or treatment effects.
  • Differential Lipid Expression — Fold-change, p-value, and FDR-adjusted analyses identifying altered plasmalogen species.
  • Ether Lipid Pathway Mapping — Integration with KEGG and LIPID MAPS pathways to visualize vinyl-ether metabolism trends.
  • Structural Annotation Review — Fragment ion–based validation of positional isomers and P-/O-ether distinctions.

Data Formats

  • Excel/CSV Tables — Ready for bioinformatics and figure generation.
  • Graphical Summary (PDF) — Includes class distributions, volcano and PCA plots, and representative MS/MS spectra.
  • Technical Notes — Brief interpretation of key findings, QC metrics, and method overview for report traceability.

Explore our Lipidomics Solutions brochure to learn more about our comprehensive lipidomics analysis platform.

Download Brochure

What Our Plasmalogen Analysis Used For

Redox Biology

Evaluate vinyl-ether lipids as endogenous antioxidants and oxidative stress markers.

Neuroscience Research

Study plasmalogen remodeling in brain membranes and synaptic lipid turnover.

Aging and Metabolism Studies

Track age-related shifts in ether lipid composition and metabolic flux.

Membrane Biophysics

Correlate plasmalogen levels with changes in membrane curvature and fluidity

Microbial and Fermentation Systems

Profile ether lipid synthesis in engineered or natural microbial strains.

Nutritional and Food Lipidomics

Quantify plasmalogen content in food sources and functional lipid products.

Sample Requirements for Plasmalogen Analysis Solutions

Sample typeMinimum amountContainerStorageHandling / notes
Plasma / Serum100 µLLow-bind microtube–80 °CRecord fasting/status and anticoagulant; avoid >1 freeze–thaw.
Whole blood200 µLEDTA tube–80 °CMix gently; separate plasma if possible before freezing.
Tissue (animal/plant)50–100 mgCryovial–80 °CSnap-freeze post-collection; note tissue type/region and wet weight.
Cell pellet≥1×106 cellsLow-bind tube–80 °CWash with cold PBS; remove media; record cell count and viability.
Microbial / Fermentation broth5–10 mL or pellet from equivalentScrew-cap tube/bottle–80 °CProvide medium composition; quench rapidly; clarify particulates if needed.
Food / Ingredient / Oil100–200 mg or 100 µLSealed vial–80 °CHomogenize; note moisture/fat content; shield from light.
CSF / Other biofluids100 µLLow-bind tube–80 °CPre-clear debris by gentle spin; document collection conditions.

General: Ship on dry ice. Use amber or foil wrap to limit oxidation and light exposure. Include sample metadata (matrix, species/strain, harvest timepoint, treatments) to support normalization and interpretation.

FAQs for Plasmalogen Analysis Service

What exactly are plasmalogens and why do researchers measure them?

Plasmalogens are ether glycerophospholipids with a vinyl-ether bond at sn-1 that influence membrane organization, signaling, and redox buffering; quantifying them helps track oxidative stress and lipid remodeling in cells and tissues.

How do you distinguish true plasmalogens (P-) from plasmanyl (O-ether) lipids?

We combine chromatographic behavior and MS/MS fragments with an optional acid-cleavage step that converts the vinyl-ether into dimethyl acetals (DMAs) for GC–MS readout—an established way to discriminate P- from O-ether species.

Why is the vinyl-ether bond confirmation step (DMA) important?

The P- and O-ether subclasses can be isobaric; verifying the vinyl-ether via acid hydrolysis→DMA prevents misassignment and strengthens structural confidence for publication-grade results.

What precautions reduce plasmalogen degradation during sample prep?

Because the vinyl-ether is oxidation- and acid-sensitive, best practice uses cold, antioxidant-supported extraction, minimal freeze–thaw, and protection from light—approaches shown to limit loss and artifactual oxidation.

Which analytical platforms are suitable for plasmalogen quantification?

High-resolution Orbitrap LC–MS for species-resolved profiling and LC–MS/MS for targeted quantitation are widely used; emerging ion-mobility strategies can further separate ether subclasses when needed.

Do plasmalogens act as antioxidants?

Yes—plasmalogens can serve as "sacrificial" antioxidants: the vinyl-ether preferentially oxidizes, helping protect polyunsaturated lipids and membrane domains from damage.

What biological or applied contexts benefit most from plasmalogen profiling?

Studies of membrane biophysics, redox biology, neurobiology, metabolism/aging, microbial ether-lipid synthesis, and food/nutritional lipidomics all leverage plasmalogen measurements to interpret structural and pathway changes.

Publications

* Our services can only be used for research purposes and Not for clinical use.

Services:


Online Inquiry

CONTACT US

Copyright © 2025 Creative Proteomics. All rights reserved.