Evidence map›Paper›PMID 26821010›Full record

ArticleMolecules (Basel, Switzerland)2016

Design of a MCoTI-Based Cyclotide with Angiotensin (1-7)-Like Activity.

Teshome Aboye, Christopher J Meeks, Subhabrata Majumder, Alexander Shekhtman, Kathleen Rodgers, Julio A Camarero

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Engineered Cyclotides with Potent Broad in Vitro and in Vivo Antimicrobial Activity.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Bioactivity-Guided Isolation of Neuritogenic Factor from the Seeds of the Gac Plant (Evidence-based complementary and alternative medicine : eCAM · 2018
    Article
  14. Review
  15. Review
  16. Cyclotides: Overview and Biotechnological Applications.Chembiochem : a European journal of chemical biology · 2017
    Review
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

6 authors at 2 institutions in 1 country.

Teshome AboyeDepartment of Pharmacology and Pharmaceutical Sciences, University of Southern California, Los Angeles, CA 90089-9121, USA. aboye@usc.edu.
Christopher J MeeksDepartment of Pharmacology and Pharmaceutical Sciences, University of Southern California, Los Angeles, CA 90089-9121, USA. meeksc@usc.edu.
Subhabrata MajumderDepartment of Chemistry, State University of New York, Albany, NY 12222, USA. smajumder@albany.edu.
Alexander ShekhtmanDepartment of Chemistry, State University of New York, Albany, NY 12222, USA. ashekhtman@albany.edu.
Kathleen RodgersDepartment of Pharmacology and Pharmaceutical Sciences, University of Southern California, Los Angeles, CA 90089-9121, USA. krodgers@usc.edu.
Julio A CamareroDepartment of Pharmacology and Pharmaceutical Sciences, University of Southern California, Los Angeles, CA 90089-9121, USA. jcamarer@usc.edu.
University of Southern California · USUniversity at Albany, State University of New York · US

Funding

Real Time (RT) In-cell NMR technology to study protein interactions in live cellsR01GM085006 · NIGMS · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI SHEKHTMAN, ALEXANDER · 2010 to 2021
$2.4M
Cell-based screening and selection of cyclotide-based capture reagents for proteiR01GM090323 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CAMARERO, JULIO A · 2009 to 2013
$2.0M
Screening and selection of specific protein-protein antagonists using ultrastable microprotein scaffoldsR01GM113636 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CAMARERO, JULIO A · 2015 to 2018
$1.3M
NIGMS NIH HHS R01 GM085006NIGMS NIH HHS R01-GM085006NIGMS NIH HHS R01 GM090323NIGMS NIH HHS R01-GM090323NIGMS NIH HHS R01-GM113363NIGMS NIH HHS R01 GM113636
6 · The paper itself

Abstract

We report for the first time the design and synthesis of a novel cyclotide able to activate the unique receptor of angiotensin (1-7) (AT1-7), the MAS1 receptor. This was accomplished by grafting an AT1-7 peptide analog onto loop 6 of cyclotide MCoTI-I using isopeptide bonds to preserve the α-amino and C-terminal carboxylate groups of AT1-7, which are required for activity. The resulting cyclotide construct was able to adopt a cyclotide-like conformation and showed similar activity to that of AT1-7. This cyclotide also showed high stability in human serum thereby providing a promising lead compound for the design of a novel type of peptide-based in the treatment of cancer and myocardial infarction.

Indexed as

Angiotensin IAnimalsCell SurvivalCHO CellsCricetulusCyclotidesHumansMyocardial InfarctionNeoplasmsPeptide FragmentsPlant ProteinsProtein ConformationProtein FoldingProtein StabilityProto-Oncogene MasProto-Oncogene ProteinsAngiotensin Iangiotensin I (1-7)CyclotidesMAS1 protein, humanMCoTI-I protein, Momordica cochinchinensisPeptide FragmentsPlant ProteinsProto-Oncogene MasProto-Oncogene ProteinsReceptors, G-Protein-CoupledangiotensincyclotideMAS1 receptor

Identifiers

PMID26821010
PMCPMC4795166
OpenAlexW2257912746

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.