Evidence map›Paper›PMID 9689111›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

Mammalian glycophosphatidylinositol anchor transfer to proteins and posttransfer deacylation.

R Chen, E I Walter, G Parker, J P Lapurga, J L Millan, Y Ikehara, S Udenfriend, M E Medof

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Nebulized mRNA-Encoded Antibodies Protect Hamsters from SARS-CoV-2 Infection.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. The Journal of cell biology · 2018
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Biosynthesis and deficiencies of glycosylphosphatidylinositol.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2014
    Review
  15. Heritable disorders in the metabolism of the dolichols: A bridge from sterol biosynthesis to molecular glycosylation.American journal of medical genetics. Part C, Seminars in medical genetics · 2012
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 3 countries.

R ChenInstitute of Pathology, Case Western Reserve University, 2085 Adelbert Road, Cleveland, OH, 44106, USA.
E I Walter
G Parker
J P Lapurga
J L Millan
Y Ikehara
S Udenfriend
M E Medof
Cancer Research Foundation · USCase Western Reserve University · USFukuoka University · JP

Funding

ROLE OF DAF IN THE COMPLEMENT CASCADE ND IN PNHR01AI023598 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI MEDOF, MELVIN EDWARD · 1985 to 2009
$3.8M
STRUCTURE AND FUNCTION OF GLYCOINOSITOLP01DK038181 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI TARTAKOFF, ALAN MICHAEL · 1987 to 1996
–
EXPERIMENTAL MODEL OF PNHR01HL055773 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI MEDOF, MELVIN EDWARD · 1996 to 1999
–
NHLBI NIH HHS HL55773NIAID NIH HHS AI23598NIAID NIH HHS R01 AI023598NIDDK NIH HHS P01DK38181
6 · The paper itself

Abstract

The glycophosphatidylinositol (GPI) anchors of proteins expressed on human erythrocytes and nucleated cells differ with respect to acylation of an inositol hydroxyl group, a structural feature that modulates their cleavability by PI-specific phospholipase C (PI-PLC). To determine how this GPI anchor modification is regulated, the precursor and protein-associated GPIs in two K562 cell transfectants (ATCC and .48) exhibiting alternatively PI-PLC-sensitive and resistant surface proteins were analyzed and the temporal relationship between GPI protein transfer and acquisition of PI-PLC sensitivity was determined. Nondenaturing PAGE analyses demonstrated that, whereas in .48 transfectants the GPI anchors in decay accelerating factor (DAF) and placental alkaline phosphatase (PLAP) were >95% acylated, in ATCC transfectants, they were 60 and 33% unsubstituted, respectively. In contrast, TLC analyses revealed that putative GPI donors in the two lines were identical and were >/=95% acylated. Studies of de novo DAF biosynthesis in HeLa cells bearing proteins with >90% unacylated anchors showed that within 5 min at 37 degreesC (or at 18 degreesC, which does not permit endoplasmic reticilum exit), >50% of the anchor in nascent 44-kDa proDAF protein exhibited PI-PLC sensitivity. In vitro analyses of the microsomal processing of miniPLAP, a truncated PLAP reporter protein, demonstrated that the anchor donor initially transferred to prominiPLAP was acylated and then progressively was deacylated. These findings indicate that (i) the anchor moiety that initially transfers to nascent proteins is acylated, (ii) inositol acylation in mature surface proteins is regulated via posttransfer deacylation, which in general is cell-specific but also can be protein-dependent, and (iii) deacylation occurs in the endoplasmic reticulum immediately after GPI transfer.

Indexed as

Protein Processing, Post-TranslationalAcylationAlkaline PhosphataseCell LineGlycosylphosphatidylinositolsHeLa CellsHumansMembrane ProteinsTransfectionAlkaline PhosphataseGlycosylphosphatidylinositolsMembrane Proteins

Identifiers

PMID9689111
PMCPMC21369
OpenAlexW2035765497

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.