Evidence map›Paper›PMID 19850928›Full record

ArticleThe Journal of biological chemistry2010

Designed auto-assembly of nanostreptabodies for rapid tissue-specific targeting in vivo.

Philippe Valadon, Bryan Darsow, Tim N Buss, Malgorzata Czarny, Noelle M Griffin, Han N Nguyen, Phil Oh, Per Borgstrom, Adrian Chrastina, Jan E Schnitzer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. A Novel Anti-CD47 Nanobody Tetramer for Cancer Therapy.Antibodies (Basel, Switzerland) · 2024
    Article
  4. Article
  5. Site-specific biotinylation of purified proteins using BirA.Methods in molecular biology (Clifton, N.J.) · 2015
    Article
  6. Article
  7. Article
  8. Particle shape enhances specificity of antibody-displaying nanoparticles.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  9. More effective nanomedicines through particle design.Small (Weinheim an der Bergstrasse, Germany) · 2011
    Review
  10. Modulation of endothelial targeting by size of antibody-antioxidant enzyme conjugates.Journal of controlled release : official journal of the Controlled Release Society · 2011
    Article
  11. Article
  12. Article
  13. Article
  14. 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.

Philippe ValadonProteogenomics Research Institute for Systems Medicine, San Diego, California 92121, USA.
Bryan Darsow
Tim N Buss
Malgorzata Czarny
Noelle M Griffin
Han N Nguyen
Phil Oh
Per Borgstrom
Adrian Chrastina
Jan E Schnitzer
Proteogenomics Research Institute for Systems Medicine · USSidney Kimmel Cancer Center · US

Funding

Targeting Vessels in TumorsP01CA104898 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$13.8M
Mapping Vascular Proteome for Organ Targeting in VivoR01HL074063 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$3.8M
Nanotechnology Platform for Targeting Solid TumorsR01CA119378 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$3.6M
TISSUE TARGETING TO ENDOTHELIUM AND ITS CAVEOLAER01HL058216 · NHLBI · SIDNEY KIMMEL CANCER CENTER · PI SCHNITZER, JAN EUGENIUSZ · 1998 to 2006
$2.8M
Proteomic Resource for Basic &Clinical Cancer ResearchR24CA095893 · NCI · SIDNEY KIMMEL CANCER CENTER · PI SCHNITZER, JAN EUGENIUSZ · 2002 to 2006
$1.9M
NCI NIH HHS P01 CA104898NCI NIH HHS P01CA104898NCI NIH HHS R01 CA119378NCI NIH HHS R01CA119378NCI NIH HHS R24 CA095893NCI NIH HHS R24CA95893NHLBI NIH HHS R01 HL058216NHLBI NIH HHS R01 HL074063NHLBI NIH HHS R01HL074063NHLBI NIH HHS R01HL58216
6 · The paper itself

Abstract

Molecular medicine can benefit greatly from antibodies that deliver therapeutic and imaging agents to select organs and diseased tissues. Yet the development of complex and defined composite nanostructures remains a challenge that requires both designed stoichiometric assembly and superior in vivo testing ability. Here, we generate nanostructures called nanostreptabodies by controlled sequential assembly of biotin-engineered antibody fragments on a streptavidin scaffold with a defined capacity for additional biotinylated payloads such as other antibodies to create bispecific antibodies as well as organic and non-organic moieties. When injected intravenously, these novel and stable nanostructures exhibit exquisite targeting with tissue-specific imaging and delivery, including rapid transendothelial transport that enhances tissue penetration. This "tinkertoy construction" strategy provides a very flexible and efficient way to link targeting vectors with reporter and/or effector agents, thereby providing virtually endless combinations potentially useful for multipurpose molecular and functional imaging in vivo as well as therapies.

Indexed as

Gene Transfer TechniquesOrgan SpecificityAnimalsAntibodiesAntibodies, BispecificAntibody FormationBase SequenceBiotinylationChromatography, High Pressure LiquidGene ExpressionGenetic VectorsHumansImmunoglobulin Fab FragmentsMiceModels, BiologicalMolecular Sequence DataAntibodiesAntibodies, BispecificImmunoglobulin Fab FragmentsStreptavidin

Identifiers

PMID19850928
PMCPMC2804220
OpenAlexW2001858511

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.