Evidence map›Paper›PMID 34164031›Full record

ArticleChemical science2020

Efficient and selective DNA modification on bacterial membranes.

Qian Tian, Yousef Bagheri, Puspam Keshri, Rigumula Wu, Kewei Ren, Qikun Yu, Bin Zhao, Mingxu You

Abstract read
In one paragraph

Article in Chemical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Recent developments in DNA-based mechanical nanodevices.Chemical communications (Cambridge, England) · 2022
    Review
  7. 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

8 authors.

Qian TianDepartment of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA mingxuyou@chem.umass.edu.
Yousef BagheriDepartment of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA mingxuyou@chem.umass.edu.ORCID https://orcid.org/0000-0001-9725-9286
Puspam KeshriDepartment of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA mingxuyou@chem.umass.edu.
Rigumula WuDepartment of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA mingxuyou@chem.umass.edu.
Kewei RenDepartment of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA mingxuyou@chem.umass.edu.
Qikun YuDepartment of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA mingxuyou@chem.umass.edu.
Bin ZhaoDepartment of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA mingxuyou@chem.umass.edu.ORCID https://orcid.org/0000-0002-0987-4586
Mingxu YouDepartment of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA mingxuyou@chem.umass.edu.ORCID https://orcid.org/0000-0003-3293-9760

Funding

Defining Mechanical Landscapes at Cell-Cell JunctionsR35GM133507 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Mingxu You · 2019 to 2026
$2.8M
NIGMS NIH HHS R35 GM133507
6 · The paper itself

Abstract

With highly precise self-assembly and programmability, DNA has been widely used as a versatile material in nanotechnology and synthetic biology. Recently, DNA-based nanostructures and devices have been engineered onto eukaryotic cell membranes for various exciting applications in the detection and regulation of cell functions. While in contrast, the potential of applying DNA nanotechnology for bacterial membrane studies is still largely underexplored, which is mainly due to the lack of tools to modify DNA on bacterial membranes. Herein, using lipid-DNA conjugates, we have developed a simple, fast, and highly efficient system to engineer bacterial membranes with designer DNA molecules. We have constructed a small library of synthetic lipids, conjugated with DNA oligonucleotides, and characterized their membrane insertion properties on various Gram-negative and Gram-positive bacteria. Simply after incubation, these lipid-DNA conjugates can be rapidly and efficiently inserted onto target bacterial membranes. Based on the membrane selectivity of these conjugates, we have further demonstrated their applications in differentiating bacterial strains and potentially in pathogen detection. These lipid-DNA conjugates are promising tools to facilitate the possibly broad usage of DNA nanotechnology for bacterial membrane analysis, functionalization, and therapy.

Identifiers

PMID34164031
PMCPMC8179310

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Registered trials

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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.