Evidence map›Paper›PMID 27241126›Full record

ArticleProtein expression and purification2016

Impact of purification conditions and history on A2A adenosine receptor activity: The role of CHAPS and lipids.

Andrea N Naranjo, Patrick M McNeely, John Katsaras, Anne Skaja Robinson

Open access · greenAbstract read
In one paragraph

Article in Protein expression and purification, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Cholesterol Dependent Activity of the Adenosine AMolecules (Basel, Switzerland) · 2022
    Article
  2. Article
  3. Article
  4. Article
  5. Functional Expression of Adenosine AInternational journal of molecular sciences · 2020
    Article
  6. Article
  7. ASLAS discovery : advancing life sciences R & D · 2017
    Article
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

4 authors at 3 institutions in 1 country.

Andrea N NaranjoDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE 19711, United States.
Patrick M McNeelyDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE 19711, United States.
John KatsarasBiology and Soft Matter Division, Neutron Sciences Directorate, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6100, United States; Department of Physics and Astronomy, The University of Tennessee, Knoxville, TN 37996-1200, United States; Joint Institute for Neutron Sciences, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6453, United States.
Anne Skaja RobinsonDepartment of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE 19711, United States; Department of Chemical and Biomolecular Engineering, 300 Lindy Boggs Laboratory, Tulane University, New Orleans, LA 70118, United States. Electronic address: asr@tulane.edu.
University of Delaware · USOak Ridge National Laboratory · USTulane University · US

Funding

COBRE on Membrane Protein Production and CharacterizationP30GM103519 · NIGMS · UNIVERSITY OF DELAWARE · PI LENHOFF, ABRAHAM M · 2012 to 2014
$3.3M
THE ROLE OF MITOCHONDRIAL TRANSPORT PROTEINS IN HEPATOCYTES AND ADIPOCYTESP30RR031160 · NCRR · UNIVERSITY OF DELAWARE · PI WOULFE, DONNA S · 2010 to 2011
$2.6M
NCRR NIH HHS P30 RR031160NIGMS NIH HHS P30 GM103519
6 · The paper itself

Abstract

The adenosine A2A receptor (A2AR) is a much-studied class A G protein-coupled receptor (GPCR). For biophysical studies, A2AR is commonly purified in a detergent mixture of dodecylmaltoside (DDM), 3-(3-cholamidopropyl) dimethylammoniopropane sulfonate (CHAPS), and cholesteryl hemisuccinate (CHS). Here we studied the effects of CHAPS on the ligand binding activity and stability of wild type, full-length human A2AR. We also tested the cholesterol requirement for maintaining the active conformation of the receptor when solubilized in detergent micelles. To this end, the receptor was purified using DDM, DDM/CHAPS, or the short hydrocarbon chain lipid 1,2-dihexanoyl-sn-glycero-3-phosphocholine (DHPC, di-6:0PC). After solubilization in DDM, DDM/CHAPS, or DHPC micelles, although A2AR was found to retain its native-like fold, its binding ability was significantly compromised compared to DDM or DDM/CHAPS with CHS. It therefore appears that although cholesterol is not needed for A2AR to retain a native-like, α-helical conformation, it may be a critical component for high affinity ligand binding. Further, this result suggests that the conformational differences between the active and inactive protein may be so subtle that commonly used spectroscopic methods are unable to differentiate between the two forms, highlighting the need for activity measurements. The studies presented in this paper also underline the importance of the protein's purification history; i.e., detergents that interact with the protein during purification affect the ligand binding properties of the receptor in an irreversible manner.

Indexed as

Cholesterol EstersCholic AcidsHumansPhospholipid EthersProtein Structure, SecondaryReceptor, Adenosine A2ARecombinant Proteins1,2-dihexadecyl-sn-glycero-3-phosphocholine3-((3-cholamidopropyl)dimethylammonium)-1-propanesulfonateCholesterol Esterscholesteryl succinateCholic AcidsPhospholipid EthersReceptor, Adenosine A2ARecombinant ProteinsCholesterolDetergentsGPCRLigand bindingLipids

Identifiers

PMID27241126
PMCPMC4947529
OpenAlexW2407800162

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.