Evidence map›Paper›PMID 29018239›Full record

ArticleNature communications2017

A blueprint for robust crosslinking of mobile species in biogels with weakly adhesive molecular anchors.

Jay Newby, Jennifer L Schiller, Timothy Wessler, Jasmine Edelstein, M Gregory Forest, Samuel K Lai

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. The kinetochore corona orchestrates chromosome congression through transient microtubule interactions.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

6 authors.

Jay NewbyDepartment of Mathematics, University of North Carolina-Chapel Hill, Chapel Hill, NC, 27599, USA.
Jennifer L SchillerDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina-Chapel Hill, Chapel Hill, NC, 27599, USA.
Timothy WesslerDepartment of Mathematics, University of North Carolina-Chapel Hill, Chapel Hill, NC, 27599, USA.
Jasmine EdelsteinUNC/NCSU Joint Department of Biomedical Engineering, University of North Carolina-Chapel Hill, Chapel Hill, NC, 27599, USA.
M Gregory ForestDepartment of Mathematics, University of North Carolina-Chapel Hill, Chapel Hill, NC, 27599, USA. forest@unc.edu.ORCID http://orcid.org/0000-0002-7718-4456
Samuel K LaiDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina-Chapel Hill, Chapel Hill, NC, 27599, USA. lai@unc.edu.

Funding

Big Data to Knowledge Training ProgramT32LM012420 · NLM · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FOREST, MARK GREGORY, KOSOROK, MICHAEL R · 2016 to 2019
$1.1M
Prevalence and characteristics of anti-PEG antibodies in humansR21EB017938 · NIBIB · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LAI, SAMUEL · 2014 to 2015
$413k
NIBIB NIH HHS R21 EB017938NLM NIH HHS T32 LM012420
6 · The paper itself

Abstract

Biopolymeric matrices can impede transport of nanoparticulates and pathogens by entropic or direct adhesive interactions, or by harnessing "third-party" molecular anchors to crosslink nanoparticulates to matrix constituents. The trapping potency of anchors is dictated by association rates and affinities to both nanoparticulates and matrix; the popular dogma is that long-lived, high-affinity bonds to both species facilitate optimal trapping. Here we present a contrasting paradigm combining experimental evidence (using IgG antibodies and Matrigel®), a theoretical framework (based on multiple timescale analysis), and computational modeling. Anchors that bind and unbind rapidly from matrix accumulate on nanoparticulates much more quickly than anchors that form high-affinity, long-lived bonds with matrix, leading to markedly greater trapping potency of multiple invading species without saturating matrix trapping capacity. Our results provide a blueprint for engineering molecular anchors with finely tuned affinities to effectively enhance the barrier properties of biogels against diverse nanoparticulate species.Biological polymeric matrices often use molecular anchors, such as antibodies, to trap nanoparticulates. Here, the authors find that anchor-matrix bonds that are weak and short-lived confer superior trapping potency, contrary to the prevailing belief that effective molecular anchors should form strong bonds to both the matrix and the nanoparticulates.

Indexed as

Models, TheoreticalAdhesivesAvidinBiomechanical PhenomenaCollagenDiffusionDrug CombinationsImmunoglobulin GLamininMonte Carlo MethodNanoparticlesPolyethylene GlycolsProteoglycansAdhesivesAvidinCollagenDrug CombinationsImmunoglobulin GLamininmatrigelneutravidinPolyethylene GlycolsProteoglycans

Identifiers

PMID29018239
PMCPMC5635012

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.