Evidence map›Paper›PMID 42487561›Full record

ArticleSmall methods2026

Pressure-Modulated, Electroosmotic Flow-Driven DNA Translocations Determine DNA Super-Structure.

Lauren S Lastra, Kevin J Freedman

Abstract read
In one paragraph

Article in Small methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Lauren S LastraDepartment of Bioengineering, University of California, Riverside, California, USA.
Kevin J FreedmanDepartment of Bioengineering, University of California, Riverside, California, USA.ORCID https://orcid.org/0000-0001-8801-4578

Funding

NanoSMS: single molecule secretome analysis for non-destructive cellular fingerprintingR35GM151115 · NIGMS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI Kevin Freedman · 2023 to 2026
$1.4M
NIGMS NIH HHS R35 GM151115NIGMS NIH HHS R35GM151115
6 · The paper itself

Abstract

Electroosmotic flow (EOF) has been increasingly studied and utilized to improve single molecule sensing of DNA and protein. Here we confirm, via PCR, that EOF is sufficiently strong enough to transit DNA through the pore despite electrophoretic force (EPF) opposing the DNA's net motion. In this study, we explore how pressure-induced fluid flow modulates the intrinsic flow profiles generated by EOF and therefore DNA capture and superstructure. Despite both modes of fluid flow having parabolic or plug-shaped flow profiles inside the pore, the fluid flow profiles exterior to the pore are quite unique and offers a methodology to alter how the DNA ultimately enter the pore. Herein, we demonstrate that pressure induced, hydrodynamic fluid flow opposing the direction of transport not only slows down but also linearizes DNA molecules during translocation. Furthermore, we show that DNA gating (i.e., turning on/off DNA passage through the pore) is possible using lower pressure biases and smaller pores than previous studies.

Indexed as

DNAElectroosmosisHydrodynamicsNucleic Acid ConformationPressureDNAbiophysicselectrophoresisfluid dynamicsnanoporenanotechnology

Identifiers

PMID42487561
PMCPMC13505674

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.