Evidence map›Paper›PMID 20858197›Full record

ReviewCurrent molecular pharmacology2010

Biological activities of natural and engineered cyclotides, a novel molecular scaffold for peptide-based therapeutics.

Angie E Garcia, Julio A Camarero

Abstract readReview
In one paragraph

Review in Current molecular pharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Biotechnological Applications of Protein Splicing.Current protein & peptide science · 2019
    Review
  13. Article
  14. Review
  15. Cyclotides: Overview and Biotechnological Applications.Chembiochem : a European journal of chemical biology · 2017
    Review
  16. Article
  17. Recombinant Expression of Cyclotides Using Split Inteins.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  18. Article
  19. Article
  20. Rapid parallel synthesis of bioactive folded cyclotides by using a tea-bag approach.Chembiochem : a European journal of chemical biology · 2015
    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

2 authors at 1 institution in 1 country.

Angie E GarciaDepartment of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90033, USA.
Julio A Camarero
University of Southern California · US

Funding

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
NIGMS NIH HHS GM090323-01NIGMS NIH HHS R01 GM090323
6 · The paper itself

Abstract

Cyclotides are a growing family of large plant-derived backbone-cyclized polypeptides (≈30 amino acids long) that share a disulfide-stabilized core characterized by an unusual knotted structure. Their unique circular backbone topology and knotted arrangement of three disulfide bonds makes them exceptionally stable to thermal, chemical, and enzymatic degradation compared to other peptides of similar size. Currently more than 100 sequences of different cyclotides have been characterized and the number is expected to increase dramatically in the coming years. Considering their stability, biological activities and ability to cross the cell membrane, cyclotides can be exploited to develop new peptide-based drugs with high potential for success. The cyclotide scaffold can be engineered or evolved using molecular evolution to inhibit protein-protein interactions implicated in cancer and other human diseases, or design new antimicrobial. The present review reports the biological diversity and therapeutic potential of natural and engineered cyclotides.

Indexed as

Protein EngineeringCyclotidesHumansInteinsRecombinant ProteinsCyclotidescycloviolacin O2kalata B1Recombinant Proteinstrypsin inhibitor MCoTI-II

Identifiers

PMID20858197
PMCPMC3328131
OpenAlexW2032537132

What OpenQuestion holds

Textmetadata
LicenceTDM
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.