Evidence map›Paper›PMID 18996193›Full record

ReviewCurrent opinion in biotechnology2008

De novo designed synthetic mimics of antimicrobial peptides.

Richard W Scott, William F DeGrado, Gregory N Tew

Abstract readReview
In one paragraph

Review in Current opinion in biotechnology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
–field-weighted citation impact
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

57 citing papers in PubMed.

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  15. Spiers Memorial Lecture: Analysis andFaraday discussions · 2021
    Article
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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

3 authors.

Richard W ScottPolyMedix, Inc., 170 N. Radnor-Chester Road, Suite 300, Radnor, PA 19087, USA. rscott@polymedix.com
William F DeGrado
Gregory N Tew

Funding

Design and mechanistic studies of mimics of antimicrobial peptidesR01AI074866 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DEGRADO, WILLIAM · 2008 to 2012
$3.0M
Therapeutic Development of Antimicrobial BiomimeticsR44AI058407 · NIAID · POLYMEDIX, INC, · PI SCOTT, RICHARD W · 2006 to 2008
$2.9M
Design and mechanistic studies of mimics of antimicrobial peptidesR56AI074866 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DEGRADO, WILLIAM · 2013 to 2013
$573k
Animal Testing of Biomimetic Antimicrobial OligomersR43AI058407 · NIAID · POLYMEDIX, INC, · PI SCOTT, RICHARD W · 2004 to 2004
$239k
NIAID NIH HHS AI74866NIAID NIH HHS R01 AI074866NIAID NIH HHS R43 AI058407NIAID NIH HHS R44 AI058407NIAID NIH HHS R56 AI074866
6 · The paper itself

Abstract

Antimicrobial peptides are small cationic amphiphiles that play an important role in the innate immune system. Given their broad specificity, they appear to be ideal therapeutic agents. As a result, over the last decade, there has been considerable interest in developing them as intravenously administered antibiotics. However, it has proven difficult to accomplish this goal with peptide-based structures. Although it has been possible to solve some relatively simple problems such as susceptibility to proteolysis, more severe problems have included the expense of the materials, toxicity, limited efficacy, and limited tissue distribution. In an effort to overcome these problems, we developed small synthetic oligomers designed to adopt amphiphilic conformations and exhibit potent antimicrobial activity while being nontoxic to host cells. One class of these synthetic mimics of antimicrobial peptides (SMAMPs) is being developed as intravenous antibiotics.

Indexed as

Molecular MimicryAnimalsAnti-Infective AgentsDrug DesignPeptidesAnti-Infective AgentsPeptides

Identifiers

PMID18996193
PMCPMC2646611

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.