Evidence map›Paper›PMID 23395956›Full record

ArticleNanotechnology2013

Nanoscale protein arrays of rich morphologies via self-assembly on chemically treated diblock copolymer surfaces.

Sheng Song, Marissa Milchak, Hebing Zhou, Thomas Lee, Mark Hanscom, Jong-in Hahm

Abstract read
In one paragraph

Article in Nanotechnology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

6 authors.

Sheng SongDepartment of Chemistry, Georgetown University, 37th and O Sts. NW, Washington, DC 20057, USA.
Marissa Milchak
Hebing Zhou
Thomas Lee
Mark Hanscom
Jong-in Hahm

Funding

ZnO Nanorod-based Early Biomarker Screening for Acute Kidney InjuryR01DK088016 · NIDDK · GEORGETOWN UNIVERSITY · PI HAHM, JONG-IN · 2010 to 2014
$1.6M
NIDDK NIH HHS 1R01DK088016-01NIDDK NIH HHS R01 DK088016
6 · The paper itself

Abstract

Well-controlled assembly of proteins on supramolecular templates of block copolymers can be extremely useful for high-throughput biodetection. We report the adsorption and assembly characteristics of a model antibody protein to various polystyrene-block-poly(4-vinylpyridine) templates whose distinctive nanoscale structures are obtained through time-regulated exposure to chloroform vapor. The strong adsorption preference of the protein to the polystyrene segment in the diblock copolymer templates leads to an easily predictable, controllable, rich set of nanoscale protein morphologies through self-assembly. We also demonstrate that the chemical identities of various subareas within individual nanostructures can be readily elucidated by investigating the corresponding protein adsorption behavior on each chemically distinct area of the template. In our approach, a rich set of intricate nanoscale morphologies of protein arrays that cannot be easily attained through other means can be generated straightforwardly via self-assembly of proteins on chemically treated diblock copolymer surfaces, without the use of clean-room-based fabrication tools. Our approach provides much-needed flexibility and versatility for the use of block copolymer-based protein arrays in biodetection. The ease of fabrication in producing well-defined and self-assembled templates can contribute to a high degree of versatility and simplicity in acquiring an intricate nanoscale geometry and spatial distribution of proteins in arrays. These advantages can be extremely beneficial both for fundamental research and biomedical detection, especially in the areas of solid-state-based, high-throughput protein sensing.

Indexed as

AdsorptionAnimalsAntibodies, Anti-IdiotypicCattleChloroformImmunoglobulin GMicroscopy, Atomic ForceModels, MolecularNanotechnologyParticle SizePolystyrenesPolyvinylsProtein Array AnalysisPyridinesSurface PropertiesAntibodies, Anti-IdiotypicChloroformImmunoglobulin Gpolystyrene-block-poly(4-vinylpyridine)PolystyrenesPolyvinylsPyridines

Identifiers

PMID23395956
PMCPMC3600641

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.