Evidence map›Paper›PMID 17369356›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Tracking melanosomes inside a cell to study molecular motors and their interaction.

Comert Kural, Anna S Serpinskaya, Ying-Hao Chou, Robert D Goldman, Vladimir I Gelfand, Paul R Selvin

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 103 citations in OpenAlex.

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  15. Fluorescence imaging with one-nanometer accuracy (FIONA).Journal of visualized experiments : JoVE · 2014
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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 2 countries.

Comert KuralCenter for Biophysics and Computational Biology and Department of Physics, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Anna S Serpinskaya
Ying-Hao Chou
Robert D Goldman
Vladimir I Gelfand
Paul R Selvin
Northwestern University · USInstitute of Molecular Biology and Biophysics · RU

Funding

REGULATION OF MYOSIN DRIVEN ORGANELLE TRANSPORTR01GM052111 · NIGMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI GELFAND, VLADIMIR I · 1999 to 2018
$8.3M
Nanometric Fluorescence Imaging of Single Motor ProteinsR01GM068625 · NIGMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI SELVIN, PAUL R · 2004 to 2012
$2.8M
GENETICALLY TARGETABLE LABELS FOR LIGHT AND EM (RMI)P20GM072033 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TSIEN, ROGER Y · 2004 to 2007
$2.5M
MICROTUBULE MOTORS--SPECIFICITY AND REGULATIONR55GM052111 · NIGMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI GELFAND, VLADIMIR I · 1995 to 1995
–
NIGMS NIH HHS GM052111NIGMS NIH HHS GM068625NIGMS NIH HHS GM072033NIGMS NIH HHS P20 GM072033NIGMS NIH HHS R01 GM052111NIGMS NIH HHS R01 GM068625
6 · The paper itself

Abstract

Cells known as melanophores contain melanosomes, which are membrane organelles filled with melanin, a dark, nonfluorescent pigment. Melanophores aggregate or disperse their melanosomes when the host needs to change its color in response to the environment (e.g., camouflage or social interactions). Melanosome transport in cultured Xenopus melanophores is mediated by myosin V, heterotrimeric kinesin-2, and cytoplasmic dynein. Here, we describe a technique for tracking individual motors of each type, both individually and in their interaction, with high spatial (approximately 2 nm) and temporal (approximately 1 msec) localization accuracy. This method enabled us to observe (i) stepwise movement of kinesin-2 with an average step size of 8 nm; (ii) smoother melanosome transport (with fewer pauses), in the absence of intermediate filaments (IFs); and (iii) motors of actin filaments and microtubules working on the same cargo nearly simultaneously, indicating that a diffusive step is not needed between the two systems of transport. In concert with our previous report, our results also show that dynein-driven retrograde movement occurs in 8-nm steps. Furthermore, previous studies have shown that melanosomes carried by myosin V move 35 nm in a stepwise fashion in which the step rise-times can be as long as 80 msec. We observed 35-nm myosin V steps in melanophores containing no IFs. We find that myosin V steps occur faster in the absence of IFs, indicating that the IF network physically hinders organelle transport.

Indexed as

ActinsAnimalsBiological TransportCell LineDyneinsIntermediate FilamentsKinesinsMelaninsMelanophoresMelanosomesMicrotubulesMolecular Motor ProteinsMyosin Type VProtein BindingXenopusActinsDyneinsKinesinsMelaninsMolecular Motor ProteinsMyosin Type V

Identifiers

PMID17369356
PMCPMC1838505
OpenAlexW2060061334

What OpenQuestion holds

Textmetadata
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.