Evidence map›Paper›PMID 37261404›Full record

ArticleACS nano2023

Evaluation of Nanopore Sensor Design Using Electrical and Optical Analyses.

Lauren A Mayse, Ali Imran, Yazheng Wang, Mohammad Ahmad, Rebecca A Oot, Stephan Wilkens, Liviu Movileanu

Abstract read
In one paragraph

Article in ACS nano, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
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  8. 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

7 authors.

Lauren A MayseDepartment of Physics, Syracuse University, 201 Physics Building, Syracuse, New York 13244-1130, United States.ORCID 0000-0001-8790-0324
Ali ImranDepartment of Physics, Syracuse University, 201 Physics Building, Syracuse, New York 13244-1130, United States.
Yazheng WangDepartment of Physics, Syracuse University, 201 Physics Building, Syracuse, New York 13244-1130, United States.
Mohammad AhmadDepartment of Physics, Syracuse University, 201 Physics Building, Syracuse, New York 13244-1130, United States.
Rebecca A OotDepartment of Biochemistry and Molecular Biology, State University of New York-Upstate Medical University, 750 East Adams Street, Syracuse, New York 13210, United States.
Stephan WilkensDepartment of Biochemistry and Molecular Biology, State University of New York-Upstate Medical University, 750 East Adams Street, Syracuse, New York 13210, United States.
Liviu MovileanuDepartment of Physics, Syracuse University, 201 Physics Building, Syracuse, New York 13244-1130, United States.ORCID 0000-0002-2525-3341

Funding

Engineered Nanopores for Single-Molecule Stochastic SensingR01GM088403 · NIGMS · SYRACUSE UNIVERSITY · PI MOVILEANU, LIVIU · 2009 to 2022
$3.8M
Structure and Regulatory Mechanisms of the Vacuolar ATPaseR35GM141908 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI WILKENS, STEPHAN · 2021 to 2025
$2.1M
Development of Modular Synthetic Sensors for Protein Biomarker DetectionR01EB033412 · NIBIB · SYRACUSE UNIVERSITY · PI LIVIU MOVILEANU · 2023 to 2026
$1.4M
NIBIB NIH HHS R01 EB033412NIGMS NIH HHS R01 GM088403NIGMS NIH HHS R35 GM141908
6 · The paper itself

Abstract

Nanopores are currently utilized as powerful tools for single-molecule protein sensing. The reporting signal typically requires protein analytes to enter the nanopore interior, yet a class of these sensors has emerged that allows targeted detection free in solution. This tactic eliminates the spatial limitation of nanopore confinement. However, probing proteins outside the nanopore implies numerous challenges associated with transducing the physical interactions in the aqueous phase into a reliable electrical signature. Hence, it necessitates extensive engineering and tedious optimization routes. These obstacles have prevented the widespread adoption of these sensors. Here, we provide an experimental strategy by developing and validating single-polypeptide-chain nanopores amenable to single-molecule and bulk-phase protein detection approaches. We utilize protein engineering, as well as nanopore and nanodisc technologies, to create nanopore sensors that can be integrated with an optical platform in addition to traditional electrical recordings. Using the optical modality over an ensemble of detectors accelerates these sensors' optimization process for a specific task. It also provides insights into how the construction of these single-molecule nanopore sensors influences their performance. These outcomes form a basis for evaluating engineered nanopores beyond the fundamental limits of the resistive-pulse technique.

Indexed as

NanoporesElectricityNanotechnologyPeptidesProteinsPeptidesProteinsbiolayer interferometrynanodiscnanosensorprotein detectionprotein engineeringreal-time kineticssingle-molecule electrophysiology

Identifiers

PMID37261404
PMCPMC10278182

What OpenQuestion holds

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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.