Evidence map›Paper›PMID 23294022›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2013

Predicting isoelectric points of nonfunctional mitochondria from Monte Carlo simulations of surface compositions.

Gregory G Wolken, Benjamin J Fossen, Ayoung Noh, Edgar A Arriaga

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 85% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

Gregory G WolkenDepartment of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Benjamin J Fossen
Ayoung Noh
Edgar A Arriaga
University of Minnesota · US

Funding

Training Grant: Functional Proteomics of AgingT32AG029796 · NIA · UNIVERSITY OF MINNESOTA · PI EDGAR A ARRIAGA, Douglas G Mashek · 2008 to 2026
$6.6M
Quantitating Mitophagy in Skeletal Muscle ModelsR01AG020866 · NIA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ARRIAGA, EDGAR A · 2002 to 2021
$5.7M
NIA NIH HHS R01 AG020866NIA NIH HHS R01-AG020866NIA NIH HHS T32 AG029796NIA NIH HHS T32-AG029796
6 · The paper itself

Abstract

Mitochondria are heterogeneous organelles involved in energy production, metabolism, and cellular signaling that oftentimes are isolated from cells for chemical characterization (e.g., proteomic analysis). The chemical composition of the mitochondrial outer membrane is one of the factors defining the mitochondrial isoelectric point (pI), which is a property useful for the analysis and characterization of isolated mitochondria. We previously used capillary isoelectric focusing (cIEF) with laser-induced-fluorescence detection to determine the experimental pI of individual mitochondria after their isolation under depolarizing conditions. This technique revealed that, when kept nonfunctional, mitochondrial pI is heterogeneous as displayed by the observed distributions of pI. To model the effect of surface composition on pI heterogeneity of these mitochondria, we devised a method to predict mitochondrial pI values using simulated surface compositions. The method was initially validated by predicting the pI values of known mitochondrial outer membrane proteins and was then extended to isolated mitochondria, in which both ionizable amino acids and phospholipids contribute to mitochondrial pI. After using a Monte Carlo method to generate a library of over 2 million possible mitochondrial surface compositions, sufficient compositions to match the frequency of occurrence of experimental mitochondrial pI values were randomly selected. This comparison allows for association of a given individual mitochondrial pI with thousands of randomly chosen compositions. The method predicts significant changes in the percentages of some amino acids and phospholipids for observed pI differences between individual mitochondria, which is an important advancement toward explaining the observed heterogeneity of mitochondrial pI.

Indexed as

Molecular Dynamics SimulationIsoelectric PointMitochondriaMitochondrial MembranesModels, MolecularMonte Carlo MethodSurface Properties

Identifiers

PMID23294022
PMCPMC3582746
OpenAlexW2317998431

What OpenQuestion holds

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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.