Evidence map›Paper›PMID 12646066›Full record

ArticleProteome science2003

Peptides identify multiple hotspots within the ligand binding domain of the TNF receptor 2.

Ku-Chuan Hsiao, Renee E Brissette, Pinger Wang, Paul W Fletcher, Vanessa Rodriguez, Michael Lennick, Arthur J Blume, Neil I Goldstein

Open access · goldAbstract read
In one paragraph

Article in Proteome science, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

2 citing papers in PubMed, 25 citations in OpenAlex.

  1. Neuronal PINCH is regulated by TNF-α and is required for neurite extension.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2011
    Article
  2. 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.

Ku-Chuan HsiaoDGI BioTechnologies, Inc, 40 Talmadge Road, Edison NJ 08818, USA. goldstein@dgibt.com
Renee E Brissette
Pinger Wang
Paul W Fletcher
Vanessa Rodriguez
Michael Lennick
Arthur J Blume
Neil I Goldstein

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHotspots are defined as the minimal functional domains involved in protein:protein interactions and sufficient to induce a biological response.

resultsHere we describe the use of complex and high diversity phage display libraries to isolate peptides (called Hotspot Ligands or HSPLs) which sub-divide the ligand binding domain of the tumor necrosis factor receptor 2 (TNFR2; p75) into multiple hotspots. We have shown that these libraries could generate HSPLs which not only subdivide hotspots on protein and non-protein targets but act as agonists or antagonists. Using this approach, we generated peptides which were specific for human TNFR2, could be competed by the natural ligands, TNFalpha and TNFbeta and induced an unexpected biological response in a TNFR2-specific manner.

conclusionsTo our knowledge, this is the first report describing the dissection of the TNFR2 into biologically active hotspots with the concomitant identification of a novel and unexpected biological activity.

Identifiers

PMID12646066
PMCPMC151557
OpenAlexW2129400167

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.