Blood bank storage of red blood cells increases RBC cytoplasmic membrane order and bending rigidity

Blood banks around the world store blood components for several weeks ensuring its availability for transfusion medicine. Red blood cells (RBCs) are known to undergo compositional changes during storage, which may impact the cells’ function and eventually the recipients’ health. We extracted the RBC...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Sebastian Himbert, Syed M. Qadri, William P. Sheffield, Peter Schubert, Angelo D’Alessandro, Maikel C. Rheinstädter
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/3ef5864f252f4669bdab478548b1ed83
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:3ef5864f252f4669bdab478548b1ed83
record_format dspace
spelling oai:doaj.org-article:3ef5864f252f4669bdab478548b1ed832021-11-25T06:11:03ZBlood bank storage of red blood cells increases RBC cytoplasmic membrane order and bending rigidity1932-6203https://doaj.org/article/3ef5864f252f4669bdab478548b1ed832021-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589153/?tool=EBIhttps://doaj.org/toc/1932-6203Blood banks around the world store blood components for several weeks ensuring its availability for transfusion medicine. Red blood cells (RBCs) are known to undergo compositional changes during storage, which may impact the cells’ function and eventually the recipients’ health. We extracted the RBC’s cytoplasmic membrane (RBCcm) to study the effect of storage on the membranes’ molecular structure and bending rigidity by a combination of X-ray diffraction (XRD), X-ray diffuse scattering (XDS) and coarse grained Molecular Dynamics (MD) simulations. Blood was stored in commercial blood bags for 2 and 5 weeks, respectively and compared to freshly drawn blood. Using mass spectrometry, we measured an increase of fatty acids together with a slight shift towards shorter tail lengths. We observe an increased fraction (6%) of liquid ordered (lo) domains in the RBCcms with storage time, and an increased lipid packing in these domains, leading to an increased membrane thickness and membrane order. The size of both, lo and liquid disordered (ld) lipid domains was found to decrease with increased storage time by up to 25%. XDS experiments reveal a storage dependent increase in the RBCcm’s bending modulus κ by a factor of 2.8, from 1.9 kBT to 5.3 kBT. MD simulations were conducted in the absence of proteins. The results show that the membrane composition has a small contribution to the increased bending rigidity and suggests additional protein-driven mechanisms.Sebastian HimbertSyed M. QadriWilliam P. SheffieldPeter SchubertAngelo D’AlessandroMaikel C. RheinstädterPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Sebastian Himbert
Syed M. Qadri
William P. Sheffield
Peter Schubert
Angelo D’Alessandro
Maikel C. Rheinstädter
Blood bank storage of red blood cells increases RBC cytoplasmic membrane order and bending rigidity
description Blood banks around the world store blood components for several weeks ensuring its availability for transfusion medicine. Red blood cells (RBCs) are known to undergo compositional changes during storage, which may impact the cells’ function and eventually the recipients’ health. We extracted the RBC’s cytoplasmic membrane (RBCcm) to study the effect of storage on the membranes’ molecular structure and bending rigidity by a combination of X-ray diffraction (XRD), X-ray diffuse scattering (XDS) and coarse grained Molecular Dynamics (MD) simulations. Blood was stored in commercial blood bags for 2 and 5 weeks, respectively and compared to freshly drawn blood. Using mass spectrometry, we measured an increase of fatty acids together with a slight shift towards shorter tail lengths. We observe an increased fraction (6%) of liquid ordered (lo) domains in the RBCcms with storage time, and an increased lipid packing in these domains, leading to an increased membrane thickness and membrane order. The size of both, lo and liquid disordered (ld) lipid domains was found to decrease with increased storage time by up to 25%. XDS experiments reveal a storage dependent increase in the RBCcm’s bending modulus κ by a factor of 2.8, from 1.9 kBT to 5.3 kBT. MD simulations were conducted in the absence of proteins. The results show that the membrane composition has a small contribution to the increased bending rigidity and suggests additional protein-driven mechanisms.
format article
author Sebastian Himbert
Syed M. Qadri
William P. Sheffield
Peter Schubert
Angelo D’Alessandro
Maikel C. Rheinstädter
author_facet Sebastian Himbert
Syed M. Qadri
William P. Sheffield
Peter Schubert
Angelo D’Alessandro
Maikel C. Rheinstädter
author_sort Sebastian Himbert
title Blood bank storage of red blood cells increases RBC cytoplasmic membrane order and bending rigidity
title_short Blood bank storage of red blood cells increases RBC cytoplasmic membrane order and bending rigidity
title_full Blood bank storage of red blood cells increases RBC cytoplasmic membrane order and bending rigidity
title_fullStr Blood bank storage of red blood cells increases RBC cytoplasmic membrane order and bending rigidity
title_full_unstemmed Blood bank storage of red blood cells increases RBC cytoplasmic membrane order and bending rigidity
title_sort blood bank storage of red blood cells increases rbc cytoplasmic membrane order and bending rigidity
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/3ef5864f252f4669bdab478548b1ed83
work_keys_str_mv AT sebastianhimbert bloodbankstorageofredbloodcellsincreasesrbccytoplasmicmembraneorderandbendingrigidity
AT syedmqadri bloodbankstorageofredbloodcellsincreasesrbccytoplasmicmembraneorderandbendingrigidity
AT williampsheffield bloodbankstorageofredbloodcellsincreasesrbccytoplasmicmembraneorderandbendingrigidity
AT peterschubert bloodbankstorageofredbloodcellsincreasesrbccytoplasmicmembraneorderandbendingrigidity
AT angelodalessandro bloodbankstorageofredbloodcellsincreasesrbccytoplasmicmembraneorderandbendingrigidity
AT maikelcrheinstadter bloodbankstorageofredbloodcellsincreasesrbccytoplasmicmembraneorderandbendingrigidity
_version_ 1718414035994542080