Evidence map›Paper›PMID 31746556›Full record

ArticleCurrent protocols in protein science2019

Preparation of Lipid Nanodiscs with Lipid Mixtures.

Mavis Jiarong Li, William M Atkins, Wynton D McClary

Open access · greenAbstract read
In one paragraph

Article in Current protocols in protein science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
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, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. The Nanodisc System for Investigating Protein-Lipid Interactions.Methods in molecular biology (Clifton, N.J.) · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Do Nanodisc Assembly Conditions Affect Natural Lipid Uptake?Journal of the American Society for Mass Spectrometry · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Rapid preparation of nanodiscs for biophysical studies.Archives of biochemistry and biophysics · 2021
    Article
  16. Article
  17. 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

3 authors at 2 institutions in 1 country.

Mavis Jiarong LiDepartment of Medicinal Chemistry, University of Washington, Seattle, Washington.
William M AtkinsDepartment of Medicinal Chemistry, University of Washington, Seattle, Washington.
Wynton D McClaryDepartment of Pharmaceutical Sciences, University of Colorado, Anschutz Medical Campus, Aurora, Colorado.
University of Washington · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Pharmacological Sciences SupplementT32GM007750 · NIGMS · UNIVERSITY OF WASHINGTON · PI ATKINS, WILLIAM M · 1985 to 2023
$12.6M
Functional Dynamics of Cytochrome P4503A4R01GM130810 · NIGMS · UNIVERSITY OF WASHINGTON · PI ATKINS, WILLIAM M · 2018 to 2021
$1.8M
Functional Dynamics of P-glycoproteinR01GM121603 · NIGMS · UNIVERSITY OF WASHINGTON · PI ATKINS, WILLIAM M · 2017 to 2020
$1.2M
NIGMS NIH HHS R01 GM121603NIGMS NIH HHS R01 GM130810NIGMS NIH HHS T32 GM007750
6 · The paper itself

Abstract

Lipid nanodiscs provide a native-like lipid environment for membrane proteins, and they have become a valuable platform for the study of membrane biophysics. A range of biophysical and biochemical analyses are enabled when membrane proteins are captured in lipid nanodiscs. Two parameters that can be controlled when capturing membrane proteins in lipid nanodiscs are the radius, and hence the surface area of the lipid surface, and the composition of the lipid bilayer. Despite their emergence as a versatile tool, most studies with lipid nanodiscs in the literature have focused on nanodiscs of a single radius with a single lipid. In light of the complexity of biological membranes, it is likely that nanodiscs with multiple membrane components would be more sophisticated models for membrane research. It is possible to prepare nanodiscs with more complex lipid mixtures to probe the effects of lipid composition on several aspects of membrane biochemistry. Detailed protocols are described here for the preparation of nanodiscs with mixtures of phospholipids, incorporation of cholesterol, and incorporation of a spectroscopic lipid probe. These protocols provide starting points for the construction of nanodiscs with more physiological membrane compositions or with useful biophysical probes. © 2019 by John Wiley & Sons, Inc. Basic Protocol 1: Assembly of mixed lipid nanodiscs Basic Protocol 2: Assembly of nanodiscs with cholesterol Basic Protocol 3: Incorporation of laurdan into nanodiscs for membrane fluidity measurements.

Indexed as

CholesterolLipid BilayersMembrane ProteinsNanostructuresPhospholipidsCholesterolLipid BilayersMembrane ProteinsPhospholipidscholesterollaurdanlipid nanodiscsmembrane proteinmixed lipids

Identifiers

PMID31746556
PMCPMC6894905
OpenAlexW2990552556

What OpenQuestion holds

Textmetadata
LicenceTDM
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.