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Continuous Analysis of the Mechanism of Activated Transbilayer Lipid Movement in Platelets

Williamson, Patrick, Bevers, Edouard M., Smeets, Edgar F., Comfurius, Paul, Schlegel, Robert A., Zwaal, Robert F. A.·1995·Biochemistry

Abstract

Dithionite reduction of fluorescent (NBD) phospholipids was used as the basis of a continuous assay of transbilayer lipid movement to the cell surface during platelet activation. This assay reveals that virtually all previously internalized phosphatidylserine passes through the external leaflet of the membrane within 90 s after activation with Ca2+ and ionophore or with thrombin and thapsigargin. We demonstrate that this lipid scrambling is reversible, bidirectional, and insensitive to the lipid headgroup. Prolonged activation gradually results in inactivation of the scramblase. The assay also reveals that activation of the scrambling activity is sensitive to the sulfhydryl reagent pyridyldithioethylamine, suggesting the involvement of a protein in the process of activated transbilayer lipid scrambling.

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Metadata

Authors
Williamson, P., Bevers, E. M., Smeets, E. F., Comfurius, P., Schlegel, R. A., & Zwaal, R. F. A.
Venue
Biochemistry
Published
1995-08-22
Volume
34
Issue
33
Pages
10448-10455
ISSN
  • 0006-2960 (ISSN-L)
  • 1520-4995
OpenAlex
W1981566975
Cited by
174
References
0
FWCI
3.91
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Continuous Analysis of the Mechanism of Activated Transbilayer Lipid Movement in Platelets. https://app.cochat.ai/papers/10.1021/bi00033a017
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Williamson, P., Bevers, E. M., Smeets, E. F., Comfurius, P., Schlegel, R. A., & Zwaal, R. F. A. (1995). Continuous Analysis of the Mechanism of Activated Transbilayer Lipid Movement in Platelets. Biochemistry. https://doi.org/10.1021/bi00033a017

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.