Evidence map›Paper›PMID 17373767›Full record

ArticleBioconjugate chemistry

Synthetic PEGylated glycoproteins and their utility in gene delivery.

Chang-po Chen, Ji-seon Kim, Dijie Liu, Garrett R Rettig, Marie A McAnuff, Molly E Martin, Kevin G Rice

Open access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. The reduced-charge melittin analogue MelP5 improves the transfection of non-viral DNA nanoparticles.Journal of peptide science : an official publication of the European Peptide Society · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Nano-vectors for efficient liver specific gene transfer.International journal of nanomedicine · 2008
    Review
  13. 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

7 authors at 1 institution in 1 country.

Chang-po ChenDivision of Medicinal and Natural Products Chemistry, College of Pharmacy, University of Iowa, Iowa City, Iowa 52242, USA.
Ji-seon Kim
Dijie Liu
Garrett R Rettig
Marie A McAnuff
Molly E Martin
Kevin G Rice
University of Iowa · US

Funding

Predoctoral Training in the Pharmacological SciencesT32GM067795 · NIGMS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2004 to 2021
$3.4M
RAMP Mediated Gene DeliveryR01GM087653 · NIGMS · UNIVERSITY OF IOWA · PI RICE, KEVIN G · 2009 to 2012
$1.2M
Sulfhydryl Cross-linked Targeted Gene DeliveryR01DK063196 · NIDDK · UNIVERSITY OF IOWA · PI RICE, KEVIN G · 2003 to 2006
$879k
NIDDK NIH HHS DK063196NIDDK NIH HHS R01 DK063196NIGMS NIH HHS R01 GM087653NIGMS NIH HHS T32 GM067795
6 · The paper itself

Abstract

PEGylated glycoproteins (PGPs) were synthesized by copolymerizing a Cys-terminated PEG-peptide, glycopeptide, and melittin peptide. Compositionally unique PGPs were prepared by varying the ratio of PEG-peptide (20-90%) and melittin (0-70%) with a constant amount of glycopeptide (10%). The PGPs were purified by RP-HPLC, and characterized for molecular weight and polydispersity by GPC-HPLC and SDS-PAGE and for composition by RP-HPLC following reduction to form monomeric peptides. PGPs formed DNA condensates of 200-300 nm in diameter that were administered to mice via the tail vein. Biodistribution studies confirmed their primary targeting to liver hepatocytes with a DNA metabolic half-life of 1 h. Upon stimulation by hydrodynamic dosing with saline, PGP DNA (5 microg) mediated luciferase expression in the liver detected by bioluminescence imaging (BLI) after 24 h. The level of gene expression mediated by PGP DNA was 5000-fold less than direct hydrodynamic dosing of an equivalent amount of DNA and was independent of the mol percent of melittin incorporated into the polymer, but dependent on the presence of galactose on PGP. The results establish the ability to prepare three-component gene delivery polymers that function in vivo. Further design improvements in fusogenic peptides for gene delivery and for the simultaneous use of a nuclear targeting strategy will be necessary to approach levels of expression mediated by the direct hydrodynamic dosing of DNA.

Indexed as

Drug Delivery SystemsGene TargetingAnimalsChromatography, High Pressure LiquidDNADrug CarriersGene ExpressionGene Transfer TechniquesGlycopeptidesGlycoproteinsLiverLuciferasesMelittenMiceMice, Inbred ICRMolecular WeightDNADrug CarriersGlycopeptidesGlycoproteinsLuciferasesMelittenPeptide FragmentsPolyethylene Glycols

Identifiers

PMID17373767
PMCPMC2653852
OpenAlexW2068477886

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.