Evidence map›Paper›PMID 28874568›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Proteoliposome-based full-length ZnT8 self-antigen for type 1 diabetes diagnosis on a plasmonic platform.

Hao Wan, Chengfeng Merriman, Mark A Atkinson, Clive H Wasserfall, Kieran M Mcgrail, Yongye Liang, Dax Fu, Hongjie Dai

Abstract readEvaluation Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Autoantibodies to Zinc Transporter 8 andJournal of diabetes research · 2022
    Article
  10. Gut Microbiota: An Important Player in Type 2 Diabetes Mellitus.Frontiers in cellular and infection microbiology · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Molecular imaging of β-cells: diabetes and beyond.Advanced drug delivery reviews · 2019
    Review
  18. Genetic, Functional, and Immunological Study of ZnT8 in Diabetes.International journal of endocrinology · 2019
    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.

Hao WanDepartment of Chemistry, Bio-X, and the Biophysics Program, Stanford University, Stanford, CA 94305.
Chengfeng MerrimanDepartment of Physiology, Johns Hopkins School of Medicine, Baltimore, MD 21205.
Mark A AtkinsonDepartment of Pathology, College of Medicine, University of Florida, Gainesville, FL 32610-0275.
Clive H WasserfallDepartment of Pathology, College of Medicine, University of Florida, Gainesville, FL 32610-0275.
Kieran M McgrailDepartment of Pathology, College of Medicine, University of Florida, Gainesville, FL 32610-0275.
Yongye LiangDepartment of Materials Science and Engineering, South University of Science and Technology of China, Shenzhen 518055, China.
Dax FuDepartment of Physiology, Johns Hopkins School of Medicine, Baltimore, MD 21205; dfu3@jhmi.edu hdai@stanford.edu.
Hongjie DaiDepartment of Chemistry, Bio-X, and the Biophysics Program, Stanford University, Stanford, CA 94305; dfu3@jhmi.edu hdai@stanford.edu.

Funding

Project 3P01AI042288 · NIAID · UNIVERSITY OF FLORIDA · PI Todd Michael Brusko · 1997 to 2026
$32.9M
Structure and Mechanism of Zinc Efflux TransportersR01GM065137 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI FU, DAX · 2002 to 2018
$5.6M
Aligned Nanofibrillar Scaffolds Enhance Angiogenesis and Viability in Ischemia: Sex Differences Administrative SupplementR01HL127113 · NHLBI · STANFORD UNIVERSITY · PI HUANG, NGAN F. · 2016 to 2020
$2.5M
NHLBI NIH HHS R01 HL127113NIAID NIH HHS P01 AI042288NIGMS NIH HHS R01 GM065137
6 · The paper itself

Abstract

Identified as a major biomarker for type 1 diabetes (T1D) diagnosis, zinc transporter 8 autoantibody (ZnT8A) has shown promise for staging disease risk and disease diagnosis. However, existing assays for ZnT8 autoantibody (ZnT8A) are limited to detection by soluble domains of ZnT8, owing to difficulties in maintaining proper folding of a full-length ZnT8 protein outside its native membrane environment. Through a combined bioengineering and nanotechnology approach, we have developed a proteoliposome-based full-length ZnT8 self-antigen (full-length ZnT8 proteoliposomes; PLR-ZnT8) for efficient detection of ZnT8A on a plasmonic gold chip (pGOLD). The protective lipid matrix of proteoliposomes improved the proper folding and structural stability of full-length ZnT8, helping PLR-ZnT8 immobilized on pGOLD (PLR-ZnT8/pGOLD) achieve high-affinity capture of ZnT8A from T1D sera. Our PLR-ZnT8/pGOLD exhibited efficient ZnT8A detection for T1D diagnosis with ∼76% sensitivity and ∼97% specificity (

Indexed as

Diabetes Mellitus, Type 1HEK293 CellsHumansProtein Array AnalysisProteolipidsZinc Transporter 8ProteolipidsproteoliposomesSLC30A8 protein, humanZinc Transporter 8autoantibodyfull-length ZnT8plasmonicproteoliposometype 1 diabetes

Identifiers

PMID28874568
PMCPMC5617307

What OpenQuestion holds

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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.