Evidence map›Paper›PMID 32359662›Full record

ArticleMethods in enzymology2020

Sample preparation for structural and functional analyses of the STRA6 receptor for retinol-binding protein.

Brianna K Costabile, Youn-Kyung Kim, Yunting Chen, Oliver B Clarke, Loredana Quadro, Filippo Mancia

Open access · greenAbstract read
In one paragraph

Article in Methods in enzymology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

6 authors at 2 institutions in 1 country.

Brianna K CostabileDepartment of Physiology and Cellular Biophysics, Columbia University Irving Medical Center, New York, NY, United States.
Youn-Kyung KimDepartment of Food Science and Rutgers Center for Lipid Research and New Jersey Institute of Food Nutrition and Health, Rutgers University, New Brunswick, NJ, United States.
Yunting ChenDepartment of Physiology and Cellular Biophysics, Columbia University Irving Medical Center, New York, NY, United States.
Oliver B ClarkeDepartment of Physiology and Cellular Biophysics, Columbia University Irving Medical Center, New York, NY, United States; Department of Anesthesiology, Columbia University Irving Medical Center, New York, NY, United States.
Loredana QuadroDepartment of Food Science and Rutgers Center for Lipid Research and New Jersey Institute of Food Nutrition and Health, Rutgers University, New Brunswick, NJ, United States.
Filippo ManciaDepartment of Physiology and Cellular Biophysics, Columbia University Irving Medical Center, New York, NY, United States. Electronic address: fm123@cumc.columbia.edu.
Columbia University Irving Medical Center · USRutgers, The State University of New Jersey · US

Funding

Structural basis of receptor-mediated cellular vitamin A uptakeR01EY027405 · NEI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI George Khelashvili, Filippo Mancia · 2017 to 2026
$4.4M
Investigating the role of intracellular calcium concentration on STRA6-mediated retinol uptakeF31EY029591 · NEI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI COSTABILE, BRIANNA KAY · 2018 to 2019
$90k
NEI NIH HHS F31 EY029591NEI NIH HHS R01 EY027405
6 · The paper itself

Abstract

STRA6 (stimulated by retinoic acid 6) is a 75kDa polytopic transmembrane protein that facilitates cellular retinol uptake from retinol-binding protein (RBP). Structural characterization of STRA6 from Danio rerio purified in detergent and reconstituted in amphipol A8-35 was achieved by single-particle cryo-electron microscopy (cryo-EM). This provided the first high-resolution snapshot of this protein, showing a novel topology of a tightly assembled homodimer, and an unexpected physiological association with calmodulin in addition to insights into its potential mechanism of function. Specifically, a large hydrophobic cavity in the center of STRA6 linked to the known site of interaction with RBP suggested a route of retinol entry into the cell by diffusion into the membrane through a lateral opening of the cavity directly into the bilayer. Moreover, the capability to produce pure and homogeneous protein has allowed previously unattainable functional characterization of STRA6 in a reconstituted system. Here, we describe detailed methods for Danio rerio STRA6 expression in insect cells, purification in detergent and reconstitution in amphipol for structural characterization by cryo-EM. Furthermore, we show reconstitution of the protein in liposomes for an in vitro proteoliposome-based assay of STRA6-mediated retinol uptake. Finally, we present methods and preliminary cryo-EM data for STRA6 incorporated in lipid-filled nanodiscs, a close to native milieu to study membrane protein structure and function.

Indexed as

Membrane ProteinsRetinol-Binding ProteinsCalmodulinCryoelectron MicroscopyProtein BindingCalmodulinMembrane ProteinsRetinol-Binding ProteinsMembrane proteinNanodisc incorporationProteoliposome uptake assaysRetinolSingle-particle cryo-electron microscopy

Identifiers

PMID32359662
PMCPMC9394758
OpenAlexW3015523909

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.