Evidence map›Paper›PMID 31484291›Full record

ReviewInternational journal of molecular sciences2019

The ZT Biopolymer: A Self-Assembling Protein Scaffold for Stem Cell Applications.

Yevheniia Nesterenko, Christopher J Hill, Jennifer R Fleming, Patricia Murray, Olga Mayans

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. 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
0.9field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Molecular insights into titin's A-band.Journal of muscle research and cell motility · 2023
    Article
  3. Article
  4. Designer Biopolymers: Self-Assembling Proteins and Nucleic Acids.International journal of molecular sciences · 2020
    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 at 2 institutions in 2 countries.

Yevheniia NesterenkoDepartment of Biology, University of Konstanz, 78457 Konstanz, Germany.
Christopher J HillDepartment of Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Liverpool L69 3BX, UK.
Jennifer R FlemingDepartment of Biology, University of Konstanz, 78457 Konstanz, Germany.ORCID 0000-0003-4016-8740
Patricia MurrayDepartment of Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Liverpool L69 3BX, UK.
Olga MayansDepartment of Biology, University of Konstanz, 78457 Konstanz, Germany. olga.mayans@uni-konstanz.de.ORCID 0000-0001-6876-8532
University of Konstanz · DEUniversity of Liverpool · GB

Funding

Medical Research Council MC_PC_17166Medical Research Council MC_PC_17195
6 · The paper itself

Abstract

The development of cell culture systems for the naturalistic propagation, self-renewal and differentiation of cells ex vivo is a high goal of molecular engineering. Despite significant success in recent years, the high cost of up-scaling cultures, the need for xeno-free culture conditions, and the degree of mimicry of the natural extracellular matrix attainable in vitro using designer substrates continue to pose obstacles to the translation of cell-based technologies. In this regard, the ZT biopolymer is a protein-based, stable, scalable, and economical cell substrate of high promise. ZT is based on the naturally occurring assembly of two human proteins: titin-Z1Z2 and telethonin. These protein building blocks are robust scaffolds that can be conveniently functionalized with full-length proteins and bioactive peptidic motifs by genetic manipulation, prior to self-assembly. The polymer is, thereby, fully encodable. Functionalized versions of the ZT polymer have been shown to successfully sustain the long-term culturing of human embryonic stem cells (hESCs), human induced pluripotent stem cells (hiPSCs), and murine mesenchymal stromal cells (mMSCs). Pluripotency of hESCs and hiPSCs was retained for the longest period assayed (4 months). Results point to the large potential of the ZT system for the creation of a modular, pluri-functional biomaterial for cell-based applications.

Indexed as

AnimalsBiopolymersCell Culture TechniquesCell DifferentiationEmbryonic Stem CellsHumansInduced Pluripotent Stem CellsMicePluripotent Stem CellsBiopolymersbiomimetic materialcell culture substratepolymer functionalizationprotein designprotein self-assemblystem cells

Identifiers

PMID31484291
PMCPMC6747707
OpenAlexW2971449553

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.