Evidence map›Paper›PMID 34575937›Full record

ArticleInternational journal of molecular sciences2021

Interactions of Truncated Menaquinones in Lipid Monolayers and Bilayers.

Cameron Van Cleave, Jordan T Koehn, Caroline Simões Pereira, Allison A Haase, Benjamin J Peters, Seth W Croslow, Kyle G McLaughlin, Katarina R Werst, Audra L Goach, Dean C Crick and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Menaquinone biosynthesis inEngineering microbiology · 2026
    Review
  2. Review
  3. Article
  4. 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

12 authors at 3 institutions in 2 countries.

Cameron Van CleaveDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.ORCID 0000-0002-0924-1738
Jordan T KoehnDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.ORCID 0000-0003-3008-6303
Caroline Simões PereiraDepartment of Biochemistry, Institutio de Química, Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP, Brazil.
Allison A HaaseDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.ORCID 0000-0001-6574-2599
Benjamin J PetersDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
Seth W CroslowDepartment of Chemistry, Monmouth College, Monmouth, IL 61462, USA.
Kyle G McLaughlinDepartment of Chemistry, Monmouth College, Monmouth, IL 61462, USA.
Katarina R WerstDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
Audra L GoachDepartment of Chemistry, Monmouth College, Monmouth, IL 61462, USA.
Dean C CrickCell and Molecular Biology Program, Colorado State University, Fort Collins, CO 80523, USA.
Guilherme Menegon ArantesDepartment of Biochemistry, Institutio de Química, Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP, Brazil.
Debbie C CransDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.ORCID 0000-0001-7792-3450
Colorado State University · USMonmouth College · USUniversidade de São Paulo · BR

Funding

Fundacao de Amparo a Pesquisa do Estado de São Paulo 2019/21856-7National Science Foundation CHE-1709564
6 · The paper itself

Abstract

Menaquinones (MK) are hydrophobic molecules that consist of a naphthoquinone headgroup and a repeating isoprenyl side chain and are cofactors used in bacterial electron transport systems to generate cellular energy. We have previously demonstrated that the folded conformation of truncated MK homologues, MK-1 and MK-2, in both solution and reverse micelle microemulsions depended on environment. There is little information on how MKs associate with phospholipids in a model membrane system and how MKs affect phospholipid organization. In this manuscript, we used a combination of Langmuir monolayer studies and molecular dynamics (MD) simulations to probe these questions on truncated MK homologues, MK-1 through MK-4 within a model membrane. We observed that truncated MKs reside farther away from the interfacial water than ubiquinones are are located closer to the phospholipid tails. We also observed that phospholipid packing does not change at physiological pressure in the presence of truncated MKs, though a difference in phospholipid packing has been observed in the presence of ubiquinones. We found through MD simulations that for truncated MKs, the folded conformation varied, but MKs location and association with the bilayer remained unchanged at physiological conditions regardless of side chain length. Combined, this manuscript provides fundamental information, both experimental and computational, on the location, association, and conformation of truncated MK homologues in model membrane environments relevant to bacterial energy production.

Indexed as

Lipid BilayersLipidsMolecular ConformationMolecular Dynamics SimulationMolecular StructurePhospholipidsTemperatureThermodynamicsVitamin K 2Lipid BilayersLipidsPhospholipidsVitamin K 2bilayerconformationLangmuir monolayerlipoquinoneMenaquinone (MK)phospholipidVitamin K2

Identifiers

PMID34575937
PMCPMC8470443
OpenAlexW3196748435

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.