Evidence map›Paper›PMID 28816007›Full record

ArticleAngewandte Chemie (International ed. in English)2017

Fluorous Phase-Directed Peptide Assembly Affords Nano-Peptisomes Capable of Ultrasound-Triggered Cellular Delivery.

Scott H Medina, Megan S Michie, Stephen E Miller, Martin J Schnermann, Joel P Schneider

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Autohydrolysis of Diglycine-Activated Succinic Esters Boosts Cellular Uptake.Angewandte Chemie (International ed. in English) · 2023
    Article
  8. Article
  9. Review
  10. Review
  11. Fluorinated peptide biomaterials.Peptide science (Hoboken, N.J.) · 2021
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Instructed-Assembly (iA): A Molecular Process for Controlling Cell Fate.Bulletin of the Chemical Society of Japan · 2018
    Article
  17. Life at the interface: Engineering bio-nanomaterials through interfacial molecular self-assembly.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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

5 authors at 2 institutions in 1 country.

Scott H MedinaDepartment of Biomedical Engineering, The Pennsylvania State University, 223 Hallowell, University Park, PA, 16802, USA.ORCID 0000-0001-5441-2164
Megan S MichieChemical Biology Laboratory, National Cancer Institute, National Institutes of Health, 376 Boyle Street, Frederick, MD, 21702-1201, USA.
Stephen E MillerChemical Biology Laboratory, National Cancer Institute, National Institutes of Health, 376 Boyle Street, Frederick, MD, 21702-1201, USA.ORCID 0000-0002-6988-2465
Martin J SchnermannChemical Biology Laboratory, National Cancer Institute, National Institutes of Health, 376 Boyle Street, Frederick, MD, 21702-1201, USA.
Joel P SchneiderChemical Biology Laboratory, National Cancer Institute, National Institutes of Health, 376 Boyle Street, Frederick, MD, 21702-1201, USA.ORCID 0000-0002-4403-7900
National Institutes of Health · USPennsylvania State University · US

Funding

Design and Utility of Novel Protienaceous BiomaterialsZIABC011313 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SCHNEIDER, JOEL · 2010 to 2025
$19.0M
Intramural NIH HHS ZIA BC011313
6 · The paper itself

Abstract

Here, we report the design, synthesis and efficacy of a new class of ultrasound (US)-sensitive self-assembled peptide-based nanoparticle. Peptisomes are prepared via templated assembly of a de novo designed peptide at the interface of fluorinated nanodroplets. Utilizing peptide assembly allows for facile particle synthesis, direct incorporation of bioactive sequences displayed from the particle corona, and the ability to easily encapsulate biologics during particle preparation using a mild solvent exchange procedure. Further, nano-peptisome size can be precisely controlled by simply modulating the starting peptide and fluorinated solvent concentrations during synthesis. Biomolecular cargo encapsulated within the particle core can be directly delivered to the cytoplasm of cells upon US-mediated rupture of the carrier. Thus, nano-peptisomes represent a novel class of US-activated carriers that can shuttle cell-impermeable biomacromolecules into cells with spatial and temporal precision.

Indexed as

UltrasonicsA549 CellsHumansMicroscopy, FluorescenceNanoparticlesOptical ImagingPhalloidinePhalloidinedrug deliverynanostructurespeptidesself-assemblyultrasound

Identifiers

PMID28816007
PMCPMC5679192
OpenAlexW2749116995

What OpenQuestion holds

Textmetadata
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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.