Evidence map›Paper›PMID 30794381›Full record

ArticleBioconjugate chemistry2019

Interactions of an Anti-Sickling Drug with Hemoglobin in Red Blood Cells from a Patient with Sickle Cell Anemia.

Michael Brad Strader, Hongying Liang, Fantao Meng, Julia Harper, David A Ostrowski, Eric R Henry, Arun S Shet, William A Eaton, Swee L Thein, Abdu I Alayash

Open access · greenAbstract readCase Reports
In one paragraph

Article in Bioconjugate chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. 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

10 authors at 2 institutions in 1 country.

Michael Brad StraderLaboratory of Biochemistry and Vascular Biology, Center for Biologics Evaluation and Research , Food and Drug Administration (FDA) , Silver Spring , Maryland 20993 , United States.
Hongying LiangLaboratory of Biochemistry and Vascular Biology, Center for Biologics Evaluation and Research , Food and Drug Administration (FDA) , Silver Spring , Maryland 20993 , United States.
Fantao MengLaboratory of Biochemistry and Vascular Biology, Center for Biologics Evaluation and Research , Food and Drug Administration (FDA) , Silver Spring , Maryland 20993 , United States.ORCID 0000-0003-2539-0589
Julia HarperLaboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Disease , National Institutes of Health , Bethesda , Maryland 20892-0520 , United States.
David A OstrowskiLaboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Disease , National Institutes of Health , Bethesda , Maryland 20892-0520 , United States.
Eric R HenryLaboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Disease , National Institutes of Health , Bethesda , Maryland 20892-0520 , United States.
Arun S ShetSickle Cell Branch, National Heart Lung and Blood Institute , National Institutes of Health , Bethesda , Maryland 20892 , United States.
William A EatonLaboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Disease , National Institutes of Health , Bethesda , Maryland 20892-0520 , United States.
Swee L TheinSickle Cell Branch, National Heart Lung and Blood Institute , National Institutes of Health , Bethesda , Maryland 20892 , United States.
Abdu I AlayashLaboratory of Biochemistry and Vascular Biology, Center for Biologics Evaluation and Research , Food and Drug Administration (FDA) , Silver Spring , Maryland 20993 , United States.ORCID 0000-0002-2899-6757
National Institutes of Health · USCenter for Biologics Evaluation and Research · US

Funding

Sickle cell disease molecular pathogenesis and drug therapyZIADK029053 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI EATON, WILLIAM · 2009 to 2025
$24.8M
Studies of the Natural History of Sickle Cell DiseaseZIAHL006233 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI THEIN, SWEE LAY · 2017 to 2025
$10.9M
Recombinant HbAp Production for In Vivo Toxicity StudiesP01HL110900 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI FRIEDMAN, JOEL M · 2012 to 2016
$10.6M
Human Specimen Collection to Support Basic and Clinical ResearchZIAHL006241 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI THEIN, SWEE LAY · 2019 to 2025
$2.8M
Intramural NIH HHS ZIA HL006233NHLBI NIH HHS P01 HL110900
6 · The paper itself

Abstract

The pathophysiology associated with sickle cell disease (SCD) includes hemolytic anemia, vaso-occlusive events, and ultimately end organ damage set off by the polymerization of deoxygenated hemoglobin S (HbS) into long fibers and sickling of red blood cells (RBCs). One approach toward mitigating HbS polymerization is to pharmacologically stabilize the oxygenated (R) conformation of HbS and thereby reduce sickling frequency and SCD pathology. GBT440 is an α-subunit-specific modifying agent that has recently been reported to increase HbS oxygen binding affinity and consequently delay in vitro polymerization. In addition, animal model studies have demonstrated the potential for GBT440 to be a suitable therapeutic for daily oral dosing in humans. Here, we report an optimized method for detecting GBT440 intermediates in human patient hemolysate using a combination of HPLC and mass spectrometry analysis. First, oxygen dissociation curves (ODCs) analyzed from patient blood showed that oxygen affinity increased in a dose dependent manner. Second, HPLC and integrated mass spectrometric analysis collectively confirmed that GBT440 labeling was specific to the α N-terminus thereby ruling out other potential ligand binding sites. Finally, the results from this optimized analytical approach allowed us to detect a stable α-specific GBT440 adduct in the patient's hemolysate in a dose dependent manner. The results and methods presented in this report could therefore potentially help therapeutic monitoring of GBT440 induced oxygen affinity and reveal critical insight into the biophysical properties of GBT440 Hb complexes.

Indexed as

Anemia, Sickle CellAntisickling AgentsBenzaldehydesErythrocytesHemoglobin, SickleHumansMolecular Docking SimulationOxygenPyrazinesPyrazolesAntisickling AgentsBenzaldehydesHemoglobin, SickleOxygenPyrazinesPyrazolesvoxelotor

Identifiers

PMID30794381
PMCPMC9148702
OpenAlexW2916479257

What OpenQuestion holds

Textmetadata
LicenceTDM
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.