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Identification and quantification of aminophospholipid molecular species on the surface of apoptotic and activated cells

Abstract

This protocol measures externalization of aminophospholipids (APLs) to the outside of the plasma membrane using mass spectrometry (MS). APL externalization occurs in numerous events, and it is relevant for transplant medicine, immunity and cancer. In this protocol, externalized APLs are chemically modified by using a cell-impermeable reagent (sulfo-NHS-biotin), and then they are isolated via a liquid:liquid extraction and quantified by reverse-phase liquid chromatography tandem MS (LC-MS/MS) against in-house-generated standards. This protocol describes a complementary method to existing assays that are not quantitative (e.g., annexin V flow cytometry), and it is applicable to the study of membrane reorganization in all cell types during apoptosis (e.g., during development, cancer, psychiatric disorders and other conditions, aging, vesiculation and cell division). The protocol takes 2–4 d, including the generation of standards.

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Figure 1: Structures of the molecular species of PE and PS externalized by human platelets on activation, apoptosis or during aging.
Figure 2: Externalization of APLs by apoptotic neutrophils.
Figure 3: Schematic representation of the detection of externalized APLs.
Figure 4
Figure 5: Negative MS/MS of biotinylated standards showing fragmentation pattern.
Figure 6: Analysis of APLs by using direct infusion and LC-MS/MS.

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References

  1. Daleke, D.L. Phospholipid flippases. J. Biol. Chem. 282, 821–825 (2007).

    Article  CAS  Google Scholar 

  2. Ravichandran, K.S. Find-me and eat-me signals in apoptotic cell clearance: progress and conundrums. J. Exp. Med. 207, 1807–1817 (2010).

    Article  CAS  Google Scholar 

  3. Heemskerk, J.W., Bevers, E.M. & Lindhout, T. Platelet activation and blood coagulation. Thromb. Haemost. 88, 186–193 (2002).

    Article  CAS  Google Scholar 

  4. Clark, S.R. et al. Characterization of platelet aminophospholipid externalization reveals fatty acids as molecular determinants that regulate coagulation. Proc. Natl. Acad. Sci. USA 110, 5875–5880 (2013).

    Article  CAS  Google Scholar 

  5. Shi, J. & Gilbert, G.E. Lactadherin inhibits enzyme complexes of blood coagulation by competing for phospholipid-binding sites. Blood 101, 2628–2636 (2003).

    Article  CAS  Google Scholar 

  6. Otzen, D.E., Blans, K., Wang, H., Gilbert, G.E. & Rasmussen, J.T. Lactadherin binds to phosphatidylserine-containing vesicles in a two-step mechanism sensitive to vesicle size and composition. Biochim. Biophys. Acta 1818, 1019–1027 (2012).

    Article  CAS  Google Scholar 

  7. Meers, P. & Mealy, T. Phospholipid determinants for annexin V binding sites and the role of tryptophan 187. Biochemistry 33, 5829–5837 (1994).

    Article  CAS  Google Scholar 

  8. Koopman, G. et al. Annexin V for flow cytometric detection of phosphatidylserine expression on B cells undergoing apoptosis. Blood 84, 1415–1420 (1994).

    CAS  PubMed  Google Scholar 

  9. Gao, C. et al. Procoagulant activity of erythrocytes and platelets through phosphatidylserine exposure and microparticles release in patients with nephrotic syndrome. Thromb. Haemost. 107, 681–689 (2012).

    Article  CAS  Google Scholar 

  10. Daleke, D.L. Regulation of transbilayer plasma membrane phospholipid asymmetry. J. Lipid Res. 44, 233–242 (2003).

    Article  CAS  Google Scholar 

  11. Andree, H.A. et al. Binding of vascular anticoagulant α (VAC α) to planar phospholipid bilayers. J. Biol. Chem. 265, 4923–4928 (1990).

    CAS  PubMed  Google Scholar 

  12. Hullin, F., Bossant, M.J. & Salem, N. Jr. Aminophospholipid molecular species asymmetry in the human erythrocyte plasma membrane. Biochim. Biophys. Acta 1061, 15–25 (1991).

    Article  CAS  Google Scholar 

  13. Schick, P.K., Kurica, K.B. & Chacko, G.K. Location of phosphatidylethanolamine and phosphatidylserine in the human platelet plasma membrane. Clin. Invest. 57, 1221–1226 (1976).

    Article  CAS  Google Scholar 

  14. Rothman, J.E. & Kennedy, E.P. Rapid transmembrane movement of newly synthesized phospholipids during membrane assembly. Proc. Natl. Acad. Sci. USA 74, 1821–1825 (1977).

    Article  CAS  Google Scholar 

  15. Hurley, W.L. & Finkelstein, E. Identification of leukocyte surface proteins. Methods Enzymol. 184, 433–1825 (1990).

    Article  Google Scholar 

  16. Bligh, E.G. & Dyer, W.J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37, 911–917 (1959).

    Article  CAS  Google Scholar 

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Acknowledgements

The studies were funded by the Wellcome Trust (V.B.O., V.J.H., P.W.C.). C.P.T. is a Marie Curie International Outgoing Fellow.

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C.P.T., S.R.C., V.J.H. and M.A. conducted the experiments; V.B.O. and C.P.T. wrote the paper; and P.W.C. edited the paper. V.B.O., S.R.C., C.P.T. and P.W.C. designed the protocols.

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Correspondence to Valerie B O'Donnell.

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The authors declare no competing financial interests.

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Thomas, C., Clark, S., Hammond, V. et al. Identification and quantification of aminophospholipid molecular species on the surface of apoptotic and activated cells. Nat Protoc 9, 51–63 (2014). https://doi.org/10.1038/nprot.2013.163

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