Evidence map›Paper›PMID 27074684›Full record

ArticleBiophysical journal2016

Distinct Interaction Modes of the Kinesin-13 Motor Domain with the Microtubule.

Chandrima Chatterjee, Matthieu P M H Benoit, Vania DePaoli, Juan D Diaz-Valencia, Ana B Asenjo, Gary J Gerfen, David J Sharp, Hernando Sosa

Abstract read
In one paragraph

Article in Biophysical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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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

8 authors.

Chandrima ChatterjeeDepartments of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York.
Matthieu P M H BenoitDepartments of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York.
Vania DePaoliDepartments of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York.
Juan D Diaz-ValenciaDepartments of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York.
Ana B AsenjoDepartments of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York.
Gary J GerfenDepartments of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York.
David J SharpDepartments of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York.
Hernando SosaDepartments of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, New York. Electronic address: hernando.sosa@einstein.yu.edu.

Funding

MECHANISM OF MICROTUBULE DYNAMICS REGULATION BY KINESINSR01GM113164 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI HERNANDO Jose SOSA · 2015 to 2026
$5.6M
Phosphoregulation of the Kinesin Motor Domain: Structure, Dynamics and FunctionR01GM097499 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GERFEN, GARY J., MA, AO · 2012 to 2015
$1.8M
Structural Basis of Kinesin Motor MovementR01GM083338 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SOSA, HERNANDO JOSE · 2009 to 2012
$1.8M
NIGMS NIH HHS R01 GM083338NIGMS NIH HHS R01GM083338NIGMS NIH HHS R01 GM097499NIGMS NIH HHS R01GM097499NIGMS NIH HHS R01 GM113164NIGMS NIH HHS R01GM113164
6 · The paper itself

Abstract

Kinesins-13s are members of the kinesin superfamily of motor proteins that depolymerize microtubules (MTs) and have no motile activity. Instead of generating unidirectional movement over the MT lattice, like most other kinesins, kinesins-13s undergo one-dimensional diffusion (ODD) and induce depolymerization at the MT ends. To understand the mechanism of ODD and the origin of the distinct kinesin-13 functionality, we used ensemble and single-molecule fluorescence polarization microscopy to analyze the behavior and conformation of Drosophila melanogaster kinesin-13 KLP10A protein constructs bound to the MT lattice. We found that KLP10A interacts with the MT in two coexisting modes: one in which the motor domain binds with a specific orientation to the MT lattice and another where the motor domain is very mobile and able to undergo ODD. By comparing the orientation and dynamic behavior of mutated and deletion constructs we conclude that 1) the Kinesin-13 class specific neck domain and loop-2 help orienting the motor domain relative to the MT. 2) During ODD the KLP10A motor-domain changes orientation rapidly (rocks or tumbles). 3) The motor domain alone is capable of undergoing ODD. 4) A second tubulin binding site in the KLP10A motor domain is not critical for ODD. 5) The neck domain is not the element preventing KLP10A from binding to the MT lattice like motile kinesins.

Indexed as

Drosophila melanogasterAnimalsDrosophila ProteinsKinesinsMicrotubulesModels, MolecularProtein BindingProtein DomainsRotationDrosophila ProteinsKinesinsKLP10A protein, Drosophila

Identifiers

PMID27074684
PMCPMC4833770

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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.