Evidence map›Paper›PMID 27233531›Full record

ArticleBiointerphases2016

Creating cellular patterns using genetically engineered, gold- and cell-binding polypeptides.

Linying Li, Chia-Kuei Mo, Ashutosh Chilkoti, Gabriel P Lopez, Nick J Carroll

Abstract read
In one paragraph

Article in Biointerphases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Graphene Oxide-Based Nanomaterials: An Insight into Retinal Prosthesis.International journal of molecular sciences · 2020
    Review
  4. 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

5 authors.

Linying LiDepartment of Biomedical Engineering, Duke University, Durham, North Carolina 27708 and Research Triangle Materials Research Science and Engineering Center (MRSEC), Durham, North Carolina 27708.
Chia-Kuei MoDepartment of Biomedical Engineering, Duke University, Durham, North Carolina 27708.
Ashutosh ChilkotiDepartment of Biomedical Engineering, Duke University, Durham, North Carolina 27708; Research Triangle Materials Research Science and Engineering Center (MRSEC), Durham, North Carolina 27708; and Department of Mechanical Engineering and Materials Science, Duke University, Durham, North Carolina 27708.
Gabriel P LopezCenter for Biomedical Engineering, Department of Chemical and Biological Engineering, University of New Mexico, Albuquerque, New Mexico 87131; Department of Biomedical Engineering, Duke University, Durham, North Carolina 27708; Research Triangle Materials Research Science and Engineering Center (MRSEC), Durham, North Carolina 27708; and Department of Mechanical Engineering and Materials Science, Duke University, Durham, North Carolina 27708.
Nick J CarrollDepartment of Biomedical Engineering, Duke University, Durham, North Carolina 27708 and Research Triangle Materials Research Science and Engineering Center (MRSEC), Durham, North Carolina 27708.

Funding

An Instrument for Negative Acoustic Contrast Bead-based Cell Sorting and StainingR21GM111584 · NIGMS · DUKE UNIVERSITY · PI YELLEN, BENJAMIN BIRON · 2014 to 2016
$544k
NIGMS NIH HHS R21 GM111584
6 · The paper itself

Abstract

Patterning cells on material surfaces is an important tool for the study of fundamental cell biology, tissue engineering, and cell-based bioassays. Here, the authors report a simple approach to pattern cells on gold patterned silicon substrates with high precision, fidelity, and stability. Cell patterning is achieved by exploiting adsorbed biopolymer orientation to either enhance (gold regions) or impede (silicon oxide regions) cell adhesion at particular locations on the patterned surface. Genetic incorporation of gold binding domains enables C-terminal chemisorption of polypeptides onto gold regions with enhanced accessibility of N-terminal cell binding domains. In contrast, the orientation of polypeptides adsorbed on the silicon oxide regions limit the accessibility of the cell binding domains. The dissimilar accessibility of cell binding domains on the gold and silicon oxide regions directs the cell adhesion in a spatially controlled manner in serum-free medium, leading to the formation of well-defined cellular patterns. The cells are confined within the polypeptide-modified gold regions and are viable for eight weeks, suggesting that bioactive polypeptide modified surfaces are suitable for long-term maintenance of patterned cells. This study demonstrates an innovative surface-engineering approach for cell patterning by exploiting distinct ligand accessibility on heterogeneous surfaces.

Indexed as

Cell AdhesionSurface PropertiesGoldHumansHuman Umbilical Vein Endothelial CellsPeptidesProtein BindingTissue EngineeringGoldPeptides

Identifiers

PMID27233531
PMCPMC4884188

What OpenQuestion holds

Textmetadata
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.