Evidence map›Paper›PMID 29044101›Full record

ArticleNature communications2017

Controlling the bioactivity of a peptide hormone in vivo by reversible self-assembly.

Myriam M Ouberai, Ana L Gomes Dos Santos, Sonja Kinna, Shimona Madalli, David C Hornigold, David Baker, Jacqueline Naylor, Laura Sheldrake, Dominic J Corkill, John Hood and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. 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
1.1field-weighted citation impact, top 26% 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, 39 citations in OpenAlex.

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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

15 authors at 2 institutions in 1 country.

Myriam M OuberaiNanoscience Centre, Department of Engineering, University of Cambridge, Cambridge, CB3 0FF, UK.
Ana L Gomes Dos SantosBiopharmaceutical Development, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
Sonja KinnaNanoscience Centre, Department of Engineering, University of Cambridge, Cambridge, CB3 0FF, UK.
Shimona MadalliCardiovascular and Metabolic Diseases, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
David C HornigoldCardiovascular and Metabolic Diseases, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
David BakerCardiovascular and Metabolic Diseases, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
Jacqueline NaylorCardiovascular and Metabolic Diseases, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
Laura SheldrakeInvivo Sciences UK, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
Dominic J CorkillRespiratory, Inflammation and Autoimmunity, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
John HoodClinical Pharmacology, Drug Metabolism and Pharmacokinetics, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
Paolo ViciniClinical Pharmacology, Drug Metabolism and Pharmacokinetics, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
Shahid UddinBiopharmaceutical Development, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
Steven BishopBiopharmaceutical development, MedImmune LLC Gaithersburg Headquarters, One MedImmune Way, Gaithersburg, MD, 20878, USA.
Paul G VarleyBiopharmaceutical Development, MedImmune Ltd., Granta Park, Cambridge, CB21 6GH, UK.
Mark E WellandNanoscience Centre, Department of Engineering, University of Cambridge, Cambridge, CB3 0FF, UK. mew10@cam.ac.uk.
University of Cambridge · GBhVIVO (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of peptides as therapeutic agents is undergoing a renaissance with the expectation of new drugs with enhanced levels of efficacy and safety. Their clinical potential will be only fully realised once their physicochemical and pharmacokinetic properties have been precisely controlled. Here we demonstrate a reversible peptide self-assembly strategy to control and prolong the bioactivity of a native peptide hormone in vivo. We show that oxyntomodulin, a peptide with potential to treat obesity and diabetes, self-assembles into a stable nanofibril formulation which subsequently dissociates to release active peptide and produces a pharmacological effect in vivo. The subcutaneous administration of the nanofibrils in rats results in greatly prolonged exposure, with a constant oxyntomodulin bioactivity detectable in serum for at least 5 days as compared to free oxyntomodulin which is undetectable after only 4 h. Such an approach is simple, cost-efficient and generic in addressing the limitations of peptide therapeutics.

Indexed as

AnimalsGlucoseInjections, SubcutaneousMaleMiceMice, Inbred C57BLObesityOxyntomodulinPeptide HormonesRatsRats, Sprague-DawleyGlucoseOxyntomodulinPeptide Hormones

Identifiers

PMID29044101
PMCPMC5647335
OpenAlexW2763066218

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.