Evidence map›Paper›PMID 24586729›Full record

ArticlePloS one2014

Catalytic signature of a heat-stable, chimeric human alkaline phosphatase with therapeutic potential.

Tina Kiffer-Moreira, Campbell R Sheen, Kellen Cristina da Silva Gasque, Mayte Bolean, Pietro Ciancaglini, Andrea van Elsas, Marc F Hoylaerts, José Luis Millán

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 71 citations in OpenAlex.

  1. A randomized Phase 1b trial evaluating the pharmacodynamics of ilofotase alfa in adults with hypophosphatasia.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2026
    Trial
  2. Trial
  3. Trial
  4. Trial
  5. Hypophosphatasia-pathophysiological understanding, preclinical data looking beyond the skeleton, and upcoming treatments.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. 2-Benzylidenebenzofuran-3(2RSC advances · 2021
    Article
  19. TNAP: A New Multitask Enzyme in Energy Metabolism.International journal of molecular sciences · 2021
    Review
  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 4 institutions in 4 countries.

Tina Kiffer-MoreiraSanford Children's Health Research Center, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America.
Campbell R SheenSanford Children's Health Research Center, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America.
Kellen Cristina da Silva GasqueSanford Children's Health Research Center, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America.
Mayte BoleanDepartamento de Química, FFCLRP-USP, Ribeirão Preto, São Paulo, Brazil.
Pietro CiancagliniDepartamento de Química, FFCLRP-USP, Ribeirão Preto, São Paulo, Brazil.
Andrea van ElsasAM-Pharma BV, Bunnik, The Netherlands.
Marc F HoylaertsDepartment of Cardiovascular Sciences, Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.
José Luis MillánSanford Children's Health Research Center, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America.
Sanford Burnham Prebys Medical Discovery Institute · USUniversidade de Ribeirão Preto · BRAM–Pharma (Netherlands) · NLKU Leuven · BE

Funding

MOLECULAR PATHOGENESIS/TREATMENT OF HYPOPHOSPHATASIAR01DE012889 · NIDCR · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MILLAN, JOSE LUIS · 1999 to 2020
$9.2M
NIDCR NIH HHS R01 DE012889NIDCR NIH HHS R01 DE12889
6 · The paper itself

Abstract

Recombinant alkaline phosphatases are becoming promising protein therapeutics to prevent skeletal mineralization defects, inflammatory bowel diseases, and treat acute kidney injury. By substituting the flexible crown domain of human intestinal alkaline phosphatase (IAP) with that of the human placental isozyme (PLAP) we generated a chimeric enzyme (ChimAP) that retains the structural folding of IAP, but displays greatly increased stability, active site Zn²⁺ binding, increased transphosphorylation, a higher turnover number and narrower substrate specificity, with comparable selectivity for bacterial lipopolysaccharide (LPS), than the parent IAP isozyme. ChimAP shows promise as a protein therapeutic for indications such as inflammatory bowel diseases, gut dysbioses and acute kidney injury.

Indexed as

Alkaline PhosphataseAmino Acid SequenceCatalysisCatalytic DomainFemaleGPI-Linked ProteinsHot TemperatureHumansIsoenzymesMolecular Sequence DataPlacentaPregnancyProtein FoldingProtein StabilityRecombinant ProteinsAlkaline PhosphataseALPI protein, humanGPI-Linked ProteinsIsoenzymesRecombinant Proteins

Identifiers

PMID24586729
PMCPMC3933536
OpenAlexW2005482276

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.