Evidence map›Paper›PMID 25418094›Full record

ArticleBiophysical journal2014

Penetration of cell membranes and synthetic lipid bilayers by nanoprobes.

Matthew R Angle, Andrew Wang, Aman Thomas, Andreas T Schaefer, Nicholas A Melosh

Erratum issuedAbstract readComparative Study
In one paragraph

Article in Biophysical journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Exploring Biophysics at the Membrane with Single-Molecule TIRF Microscopy.Advances in experimental medicine and biology · 2026
    Review
  2. Assessing the Feasibility of DevelopingFrontiers in neuroscience · 2021
    Article
  3. Article
  4. Nanoneedle-Based Materials for Intracellular Studies.Advances in experimental medicine and biology · 2021
    Article
  5. Article
  6. Article
  7. Review
  8. High-Aspect-Ratio Nanostructured Surfaces as Biological Metamaterials.Advanced materials (Deerfield Beach, Fla.) · 2020
    Review
  9. Article
  10. Low-Impedance 3D PEDOT:PSS Ultramicroelectrodes.Frontiers in neuroscience · 2020
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Matthew R AngleDepartment of Materials Science and Engineering, Stanford University, Stanford, California.
Andrew WangDepartment of Materials Science and Engineering, Stanford University, Stanford, California.
Aman ThomasDepartment of Materials Science and Engineering, Stanford University, Stanford, California.
Andreas T SchaeferDepartment of Materials Science and Engineering, Stanford University, Stanford, California.
Nicholas A MeloshDepartment of Materials Science and Engineering, Stanford University, Stanford, California. Electronic address: nmelosh@stanford.edu.

Funding

Medical Research Council MC_UP_1202/5
6 · The paper itself

Abstract

Nanoscale devices have been proposed as tools for measuring and controlling intracellular activity by providing electrical and/or chemical access to the cytosol. Unfortunately, nanostructures with diameters of 50-500 nm do not readily penetrate the cell membrane, and rationally optimizing nanoprobes for cell penetration requires real-time characterization methods that are capable of following the process of membrane penetration with nanometer resolution. Although extensive work has examined the rupture of supported synthetic lipid bilayers, little is known about the applicability of these model systems to living cell membranes with complex lipid compositions, cytoskeletal attachment, and membrane proteins. Here, we describe atomic force microscopy (AFM) membrane penetration experiments in two parallel systems: live HEK293 cells and stacks of synthetic lipid bilayers. By using the same probes in both systems, we were able to clearly identify membrane penetration in synthetic bilayers and compare these events with putative membrane penetration events in cells. We examined membrane penetration forces for three tip geometries and 18 chemical modifications of the probe surface, and in all cases the median forces required to penetrate cellular and synthetic lipid bilayers with nanoprobes were greater than 1 nN. The penetration force was sensitive to the probe's sharpness, but not its surface chemistry, and the force did not depend on cell surface or cytoskeletal properties, with cells and lipid stacks yielding similar forces. This systematic assessment of penetration under various mechanical and chemical conditions provides insights into nanoprobe-cell interactions and informs the design of future intracellular nanoprobes.

Indexed as

ActinsCell MembraneCytoskeletonHEK293 CellsHumansLipid BilayersMicroscopy, Atomic ForceMicroscopy, Electron, ScanningNanostructuresSurface PropertiesActinsLipid Bilayers

Identifiers

PMID25418094
PMCPMC4223211

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.