dc.contributor.author
Guerrero, Paula A.
dc.contributor.author
Murakami, Yoshiko
dc.contributor.author
Malik, Ankita
dc.contributor.author
Seeberger, Peter H.
dc.contributor.author
Kinoshita, Taroh
dc.contributor.author
Varón Silva, Daniel
dc.date.accessioned
2022-01-07T10:59:27Z
dc.date.available
2022-01-07T10:59:27Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/33374
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-33095
dc.description.abstract
The attachment of proteins to the cell membrane using a glycosylphosphatidylinositol (GPI) anchor is a ubiquitous process in eukaryotic cells. Deficiencies in the biosynthesis of GPIs and the concomitant production of GPI-anchored proteins lead to a series of rare and complicated disorders associated with inherited GPI deficiencies (IGDs) in humans. Currently, there is no treatment for patients suffering from IGDs. Here, we report the design, synthesis, and use of GPI fragments to rescue the biosynthesis of GPI-anchored proteins (GPI-APs) caused by mutation in genes involved in the assembly of GPI-glycolipids in cells. We demonstrated that the synthetic fragments GlcNAc-PI (1), Man-GlcN-PI (5), and GlcN-PI with two (3) and three lipid chains (4) rescue the deletion of the GPI biosynthesis in cells devoid of the PIGA, PIGL, and PIGW genes in vitro. The compounds allowed for concentration-dependent recovery of GPI biosynthesis and were highly active on the cytoplasmic face of the endoplasmic reticulum membrane. These synthetic molecules are leads for the development of treatments for IGDs and tools to study GPI-AP biosynthesis.
en
dc.format.extent
10 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Peptides and proteins
en
dc.subject
Biosynthesis
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie
dc.title
Rescue of Glycosylphosphatidylinositol-Anchored Protein Biosynthesis Using Synthetic Glycosylphosphatidylinositol Oligosaccharides
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1021/acschembio.1c00465
dcterms.bibliographicCitation.journaltitle
ACS Chemical Biology
dcterms.bibliographicCitation.number
11
dcterms.bibliographicCitation.pagestart
2297
dcterms.bibliographicCitation.pageend
2306
dcterms.bibliographicCitation.volume
16
dcterms.bibliographicCitation.url
https://doi.org/10.1021/acschembio.1c00465
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie

refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1554-8937
refubium.resourceType.provider
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