Evidence map›Paper›PMID 34977584›Full record

ArticleRSC chemical biology2021

Activation of a G protein-coupled receptor through indirect antibody-mediated tethering of ligands.

Ross W Cheloha, Fabian A Fischer, Thomas J Gardella, Hidde L Ploegh

Open access · goldAbstract read
In one paragraph

Article in RSC chemical biology, 2021. 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
2.2field-weighted citation impact, top 12% 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, 19 citations in OpenAlex.

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  13. Enzymatic C-to-C Protein Ligation.Angewandte Chemie (International ed. in English) · 2022
    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

4 authors at 2 institutions in 1 country.

Ross W ChelohaProgram in Cellular and Molecular Medicine, Boston Children's Hospital, 1 Blackfan Circle Boston MA 02115 USA ross.cheloha@nih.gov hidde.ploegh@childrens.harvard.edu.ORCID https://orcid.org/0000-0001-9871-8333
Fabian A FischerProgram in Cellular and Molecular Medicine, Boston Children's Hospital, 1 Blackfan Circle Boston MA 02115 USA ross.cheloha@nih.gov hidde.ploegh@childrens.harvard.edu.
Thomas J GardellaMassachusetts General Hospital and Harvard Medical School, 50 Blossom Street Boston MA 02114 USA.
Hidde L PloeghProgram in Cellular and Molecular Medicine, Boston Children's Hospital, 1 Blackfan Circle Boston MA 02115 USA ross.cheloha@nih.gov hidde.ploegh@childrens.harvard.edu.ORCID https://orcid.org/0000-0002-1090-6071
Boston Children's Hospital · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies raised against many cell surface proteins, including G protein-coupled receptors, remain important tools for their functional characterization. By linking antibodies to ligands for cell surface proteins, such adducts can be targeted to the surface of a cell type of choice. Site-specific functionalization of full-size antibodies with synthetic moieties remains challenging. Here we present new approaches in which single domain antibodies (known as VHHs or nanobodies) that target either cell surface proteins or conventional antibodies are used to indirectly deliver ligands for GPCRs to their sites of action. The combination of high yield production of nanobodies, facile site-specific functionalization, and compatibility with commercially available mouse and rabbit antibodies should enable wide application of this approach.

Identifiers

PMID34977584
PMCPMC8637866
OpenAlexW3205837077

What OpenQuestion holds

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LicenceCC BY-NC
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.