Evidence map›Paper›PMID 31101905›Full record

ArticleNature protocols2019

A nanostructure platform for live-cell manipulation of membrane curvature.

Xiao Li, Laura Matino, Wei Zhang, Lasse Klausen, Allister F McGuire, Claudia Lubrano, Wenting Zhao, Francesca Santoro, Bianxiao Cui

Abstract read
In one paragraph

Article in Nature protocols, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

  1. How Neuromorphic Microstructures Control In Vitro Early-Stage Neuronal Outgrowth.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  19. Coaching ribosome biogenesis from the nuclear periphery.bioRxiv : the preprint server for biology · 2024
    Article
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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

9 authors.

Xiao LiDepartment of Chemistry, Stanford University, Stanford, CA, USA.
Laura MatinoCenter for Advanced Biomaterials for Healthcare, Istituto Italiano di Tecnologia, Naples, Italy.ORCID http://orcid.org/0000-0002-8130-2953
Wei ZhangDepartment of Chemistry, Stanford University, Stanford, CA, USA.
Lasse KlausenDepartment of Chemistry, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0003-3004-5958
Allister F McGuireDepartment of Chemistry, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-6388-2934
Claudia LubranoCenter for Advanced Biomaterials for Healthcare, Istituto Italiano di Tecnologia, Naples, Italy.
Wenting ZhaoSchool of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore, Singapore. wtzhao@ntu.edu.sg.ORCID http://orcid.org/0000-0002-6143-5185
Francesca SantoroCenter for Advanced Biomaterials for Healthcare, Istituto Italiano di Tecnologia, Naples, Italy. francesca.santoro@iit.it.
Bianxiao CuiDepartment of Chemistry, Stanford University, Stanford, CA, USA. bcui@stanford.edu.

Funding

Developing nanoscale electrophysiology sensors for robust intracellular recordingR01GM125737 · NIGMS · STANFORD UNIVERSITY · PI CUI, BIANXIAO · 2017 to 2020
$1.4M
The role of membrane curvature in surface nanotopography-induced cell functionsR01GM128142 · NIGMS · STANFORD UNIVERSITY · PI CUI, BIANXIAO · 2018 to 2020
$1.2M
NIGMS NIH HHS R01 GM125737NIGMS NIH HHS R01 GM128142
6 · The paper itself

Abstract

Membrane curvatures are involved in essential cellular processes, such as endocytosis and exocytosis, in which they are believed to act as microdomains for protein interactions and intracellular signaling. These membrane curvatures appear and disappear dynamically, and their locations are difficult or impossible to predict. In addition, the size of these curvatures is usually below the diffraction limit of visible light, making it impossible to resolve their values using live-cell imaging. Therefore, precise manipulation of membrane curvature is important to understanding how membrane curvature is involved in intracellular processes. Recent studies show that membrane curvatures can be induced by surface topography when cells are in direct contact with engineered substrates. Here, we present detailed procedures for using nanoscale structures to manipulate membrane curvatures and probe curvature-induced phenomena in live cells. We first describe detailed procedures for the design of nanoscale structures and their fabrication using electron-beam (E-beam) lithography. The fabrication process takes 2 d, but the resultant chips can be cleaned and reused repeatedly over the course of 2 years. Then we describe how to use these nanostructures to manipulate local membrane curvatures and probe intracellular protein responses, discussing surface coating, cell plating, and fluorescence imaging in detail. Finally, we describe a procedure to characterize the nanostructure-cell membrane interface using focused ion beam and scanning electron microscopy (FIB-SEM). Nanotopography-based methods can induce stable membrane curvatures with well-defined curvature values and locations in live cells, which enables the generation of a library of curvatures for probing curvature-related intracellular processes.

Indexed as

NanostructuresAnimalsCell CommunicationCell Culture TechniquesCell LineCell MembraneChlorocebus aethiopsCOS CellsEndocytosisEquipment DesignHumansMiceMicromanipulationMicroscopy, Electron, ScanningOptical ImagingProteinsProteins

Identifiers

PMID31101905
PMCPMC6716504

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.