Evidence map›Paper›PMID 27116246›Full record

ArticlePloS one2016

Molecular Self-Assembly Strategy for Generating Catalytic Hybrid Polypeptides.

Yoshiaki Maeda, Justin Fang, Yasuhiro Ikezoe, Douglas H Pike, Vikas Nanda, Hiroshi Matsui

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. 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
0.7field-weighted citation impact, top 28% 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, 7 citations in OpenAlex.

  1. Review
  2. Catalytic peptide assemblies.Chemical Society reviews · 2018
    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 3 institutions in 1 country.

Yoshiaki MaedaDepartment of Chemistry, Hunter College and the Graduate Center, City University of New York, New York, New York, United State of America.
Justin FangDepartment of Chemistry, Hunter College and the Graduate Center, City University of New York, New York, New York, United State of America.
Yasuhiro IkezoeDepartment of Chemistry, Hunter College and the Graduate Center, City University of New York, New York, New York, United State of America.
Douglas H PikeDepartment of Biochemistry, Center for Advanced Biotechnology and Medicine and the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United State of America.
Vikas NandaDepartment of Biochemistry, Center for Advanced Biotechnology and Medicine and the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United State of America.
Hiroshi MatsuiDepartment of Chemistry, Hunter College and the Graduate Center, City University of New York, New York, New York, United State of America.
City University of New York · USHunter College · USRutgers, The State University of New Jersey · US

Funding

Basic and Translational Research Center for Reducing Health DisparitiesG12MD007599 · NIMHD · HUNTER COLLEGE · PI ANGULO, JESUS A · 2012 to 2017
$14.6M
Computational Design of a Synthetic Extracellular MatrixDP2OD006478 · OD · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI NANDA, VIKAS · 2009 to 2009
$2.3M
A Computational Approach to Developing Heterochiral Peptide TherapeuticsR01GM089949 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI NANDA, VIKAS · 2010 to 2014
$1.5M
NIGMS NIH HHS R01 GM089949NIH HHS DP2 OD006478NIMHD NIH HHS G12 MD007599
6 · The paper itself

Abstract

Recently, catalytic peptides were introduced that mimicked protease activities and showed promising selectivity of products even in organic solvents where protease cannot perform well. However, their catalytic efficiency was extremely low compared to natural enzyme counterparts presumably due to the lack of stable tertiary fold. We hypothesized that assembling these peptides along with simple hydrophobic pockets, mimicking enzyme active sites, could enhance the catalytic activity. Here we fused the sequence of catalytic peptide CP4, capable of protease and esterase-like activities, into a short amyloidogenic peptide fragment of Aβ. When the fused CP4-Aβ construct assembled into antiparallel β-sheets and amyloid fibrils, a 4.0-fold increase in the hydrolysis rate of p-nitrophenyl acetate (p-NPA) compared to neat CP4 peptide was observed. The enhanced catalytic activity of CP4-Aβ assembly could be explained both by pre-organization of a catalytically competent Ser-His-acid triad and hydrophobic stabilization of a bound substrate between the triad and p-NPA, indicating that a design strategy for self-assembled peptides is important to accomplish the desired functionality.

Indexed as

Amino Acid SequenceAmyloid beta-PeptidesCatalysisCatalytic DomainHydrophobic and Hydrophilic InteractionsMolecular Dynamics SimulationPeptide FragmentsPeptidesProtein MultimerizationRecombinant Fusion ProteinsAmyloid beta-PeptidesPeptide FragmentsPeptidesRecombinant Fusion Proteins

Identifiers

PMID27116246
PMCPMC4846159
OpenAlexW2344634632

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.