Evidence map›Paper›PMID 18576649›Full record

ArticleJournal of the American Chemical Society2008

Rational design of protein-based MRI contrast agents.

Jenny J Yang, Jianhua Yang, Lixia Wei, Omar Zurkiya, Wei Yang, Shunyi Li, Jin Zou, Yubin Zhou, Anna L Wilkins Maniccia, Hui Mao and 7 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

55 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
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  12. Recent Advances in Gene Therapy for Cancer Theranostics.Current opinion in biomedical engineering · 2021
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  15. Review
  16. Molecular Sensing with Host Systems for HyperpolarizedMolecules (Basel, Switzerland) · 2020
    Review
  17. Design of Calcium-Binding Proteins to Sense Calcium.Molecules (Basel, Switzerland) · 2020
    Review
  18. Article
  19. Review
  20. Review
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

17 authors at 2 institutions in 1 country.

Jenny J YangDepartment of Chemistry, Center for Drug Design and Advanced Biotechnology, Georgia State University, Atlanta, Georgia 30303, USA. chejjy@langate.gsu.edu
Jianhua Yang
Lixia Wei
Omar Zurkiya
Wei Yang
Shunyi Li
Jin Zou
Yubin Zhou
Anna L Wilkins Maniccia
Hui Mao
Fuqiang Zhao
Russell Malchow
Shumin Zhao
Julian Johnson
Xiaoping Hu
Eirik Krogstad
Zhi-Ren Liu
Georgia State University · USEmory University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
Designing Magnetic Resonance Protein-based Contrast Agents with High RelaxivityR01EB007268 · NIBIB · GEORGIA STATE UNIVERSITY · PI YANG, JENNY J. · 2007 to 2015
$3.1M
Biochemical Characterization of p68 RNA HelicaseR01GM063874 · NIGMS · GEORGIA STATE UNIVERSITY · PI LIU, ZHI-REN · 2003 to 2007
$1.1M
Rational Design and Analysis of Calcium Binding ProteinR01GM062999 · NIGMS · GEORGIA STATE UNIVERSITY · PI YANG, JENNY J · 2001 to 2005
$991k
NCI NIH HHS CA120181NIBIB NIH HHS EB007268NIBIB NIH HHS R01 EB007268NIGMS NIH HHS GM 063874NIGMS NIH HHS GM 62999NIGMS NIH HHS R01 GM062999NIGMS NIH HHS R01 GM063874NIGMS NIH HHS T32 GM008169
6 · The paper itself

Abstract

We describe the rational design of a novel class of magnetic resonance imaging (MRI) contrast agents with engineered proteins (CAi.CD2, i = 1, 2,..., 9) chelated with gadolinium. The design of protein-based contrast agents involves creating high-coordination Gd(3+) binding sites in a stable host protein using amino acid residues and water molecules as metal coordinating ligands. Designed proteins show strong selectivity for Gd(3+) over physiological metal ions such as Ca(2+), Zn(2+), and Mg(2+). These agents exhibit a 20-fold increase in longitudinal and transverse relaxation rate values over the conventional small-molecule contrast agents, e.g., Gd-DTPA (diethylene triamine pentaacetic acid), used clinically. Furthermore, they exhibit much stronger contrast enhancement and much longer blood retention time than Gd-DTPA in mice. With good biocompatibility and potential functionalities, these protein contrast agents may be used as molecular imaging probes to target disease markers, thereby extending applications of MRI.

Indexed as

AnimalsAntibodiesCD2 AntigensContrast MediaGadoliniumGadolinium DTPAKineticsMagnetic Resonance ImagingMetalloproteinsMiceModels, MolecularAntibodiesCa1 antibodyCD2 AntigensContrast MediaGadoliniumGadolinium DTPAMetalloproteins

Identifiers

PMID18576649
PMCPMC2692035
OpenAlexW2015792302

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.