Evidence map›Paper›PMID 33785892›Full record

ArticleNature chemistry2021

Sorting sub-150-nm liposomes of distinct sizes by DNA-brick-assisted centrifugation.

Yang Yang, Zhenyong Wu, Laurie Wang, Kaifeng Zhou, Kai Xia, Qiancheng Xiong, Longfei Liu, Zhao Zhang, Edwin R Chapman, Yong Xiong and 4 more

Abstract read
In one paragraph

Article in Nature chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Controlling membrane tension by dynamic DNA nanorings.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. DNA-Assisted Assays for Studying Lipid Transfer Between Membranes.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Size-Selective Capturing of Exosomes Using DNA Tripods.Journal of the American Chemical Society · 2024
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Yang Yang *Department of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.
Zhenyong Wu *Nanobiology Institute, Yale University, West Haven, CT, USA.
Laurie WangDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.
Kaifeng ZhouDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA.
Kai XiaInstitutes of Biomedical Sciences, Fudan University, Shanghai, China.
Qiancheng XiongDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-9897-7391
Longfei LiuDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-5760-2964
Zhao ZhangHoward Hughes Medical Institute, Department of Neuroscience, University of Wisconsin-Madison, Madison, WI, USA.
Edwin R ChapmanHoward Hughes Medical Institute, Department of Neuroscience, University of Wisconsin-Madison, Madison, WI, USA.ORCID http://orcid.org/0000-0001-9787-8140
Yong XiongDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-9625-9313
Thomas J MeliaDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.
Erdem KaratekinNanobiology Institute, Yale University, West Haven, CT, USA.ORCID http://orcid.org/0000-0002-5934-8728
Hongzhou GuInstitutes of Biomedical Sciences, Fudan University, Shanghai, China. hongzhou.gu@fudan.edu.cn.ORCID http://orcid.org/0000-0001-5058-4815
Chenxiang LinDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT, USA. chenxiang.lin@yale.edu.ORCID http://orcid.org/0000-0001-7041-1946

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Synaptotagmin C2B Domain as a Ca2+ Sensing ModuleR01MH061876 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI Edwin R Chapman · 2002 to 2026
$7.7M
Regulation of Autophagosome Membrane Dynamics by the AtgB Family of ProteinsR01GM100930 · NIGMS · YALE UNIVERSITY · PI MELIA, THOMAS JAMES · 2013 to 2024
$5.4M
Structure and dynamics of exocytotic fusion poresR35NS097362 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI CHAPMAN, EDWIN R · 2017 to 2024
$4.6M
Autophagy and NeurodegenerationR01NS063973 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MELIA, THOMAS JAMES, YAMAMOTO, AI · 2008 to 2019
$3.8M
Cell-free membrane remodeling guided by DNA nano-templatesDP2GM114830 · NIGMS · YALE UNIVERSITY · PI LIN, CHENXIANG · 2014 to 2014
$2.5M
Nucleation and dynamics of exocytotic fusion poresR01NS113236 · NINDS · YALE UNIVERSITY · PI KARATEKIN, ERDEM · 2019 to 2023
$1.8M
SYNAPTOTAGMIN IN EXCITATION/SECRETION COUPLINGR01GM056827 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI CHAPMAN, EDWIN R · 1998 to 2006
$1.8M
A Nanomechanical Toolkit to Guide Membrane Structure and DynamicsR01GM132114 · NIGMS · YALE UNIVERSITY · PI LIN, CHENXIANG · 2019 to 2022
$1.3M
Generating nuclear pore complex mimics with DNA origamiR21GM109466 · NIGMS · YALE UNIVERSITY · PI LIN, CHENXIANG, LUSK, CHARLES PATRICK · 2014 to 2015
$458k
Howard Hughes Medical InstituteNCATS NIH HHS UL1 TR001863NIGMS NIH HHS DP2 GM114830NIGMS NIH HHS R01 GM056827NIGMS NIH HHS R01 GM100930NIGMS NIH HHS R01 GM132114NIGMS NIH HHS R21 GM109466NIMH NIH HHS R01 MH061876NINDS NIH HHS R01 NS063973NINDS NIH HHS R01 NS113236NINDS NIH HHS R35 NS097362
6 · The paper itself

Abstract

In cells, myriad membrane-interacting proteins generate and maintain curved membrane domains with radii of curvature around or below 50 nm. To understand how such highly curved membranes modulate specific protein functions, and vice versa, it is imperative to use small liposomes with precisely defined attributes as model membranes. Here, we report a versatile and scalable sorting technique that uses cholesterol-modified DNA 'nanobricks' to differentiate hetero-sized liposomes by their buoyant densities. This method separates milligrams of liposomes, regardless of their origins and chemical compositions, into six to eight homogeneous populations with mean diameters of 30-130 nm. We show that these uniform, leak-resistant liposomes serve as ideal substrates to study, with an unprecedented resolution, how membrane curvature influences peripheral (ATG3) and integral (SNARE) membrane protein activities. Compared with conventional methods, our sorting technique represents a streamlined process to achieve superior liposome size uniformity, which benefits research in membrane biology and the development of liposomal drug-delivery systems.

Indexed as

Autophagy-Related Protein 7CentrifugationCholesterolDNALiposomesParticle SizeSNARE ProteinsAutophagy-Related Protein 7CholesterolDNALiposomesSNARE Proteins

Identifiers

PMID33785892
PMCPMC8049973

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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.