TY - JOUR
T1 - Non-invasive force measurement reveals the number of active kinesins on a synaptic vesicle precursor in axonal transport regulated by ARL-8
AU - Hayashi, Kumiko
AU - Hasegawa, Shin
AU - Sagawa, Takashi
AU - Tasaki, Sohei
AU - Niwa, Shinsuke
N1 - Funding Information:
We thank Dr Y. Okada for assistance with the initial planning of the study; Mr Y. Saito, and Ms S. Sato for help with the experiments; and the members belonging to the Innovative Areas ‘‘Soft Molecular Systems’’ and the young scientists of FRIS, Tohoku University for discussions about the study. This work was supported by PRIME (grant number JP17gm5810009h0003), AMED, MEXT KAKENHI (grant numbers 26104501, 26115702 and 16H00819), and JSPS KAKENHI (grant number 26310204) to K. H., as well as by the grant from Daiichi Sankyo Foundation of Life Science and JSPS KAKENHI (grant numbers 17H0510) to S. N.
Publisher Copyright:
© 2018 the Owner Societies.
PY - 2018/2/7
Y1 - 2018/2/7
N2 - Kinesin superfamily protein UNC-104, a member of the kinesin-3 family, transports synaptic vesicle precursors (SVPs). In this study, the number of active UNC-104 molecules hauling a single SVP in axons in the worm Caenorhabditis elegans was counted by applying a newly developed non-invasive force measurement technique. The distribution of the force acting on a SVP transported by UNC-104 was spread out over several clusters, implying the presence of several force-producing units (FPUs). We then compared the number of FPUs in the wild-type worms with that in arl-8 gene-deletion mutant worms. ARL-8 is a SVP-bound arf-like small guanosine triphosphatase, and is known to promote unlocking of the autoinhibition of the motor, which is critical for avoiding unnecessary consumption of adenosine triphosphate when the motor does not bind to a SVP. There were fewer FPUs in the arl-8 mutant worms. This finding indicates that a lack of ARL-8 decreased the number of active UNC-104 motors, which then led to a decrease in the number of motors responsible for SVP transport.
AB - Kinesin superfamily protein UNC-104, a member of the kinesin-3 family, transports synaptic vesicle precursors (SVPs). In this study, the number of active UNC-104 molecules hauling a single SVP in axons in the worm Caenorhabditis elegans was counted by applying a newly developed non-invasive force measurement technique. The distribution of the force acting on a SVP transported by UNC-104 was spread out over several clusters, implying the presence of several force-producing units (FPUs). We then compared the number of FPUs in the wild-type worms with that in arl-8 gene-deletion mutant worms. ARL-8 is a SVP-bound arf-like small guanosine triphosphatase, and is known to promote unlocking of the autoinhibition of the motor, which is critical for avoiding unnecessary consumption of adenosine triphosphate when the motor does not bind to a SVP. There were fewer FPUs in the arl-8 mutant worms. This finding indicates that a lack of ARL-8 decreased the number of active UNC-104 motors, which then led to a decrease in the number of motors responsible for SVP transport.
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U2 - 10.1039/c7cp05890j
DO - 10.1039/c7cp05890j
M3 - Article
C2 - 29349444
AN - SCOPUS:85041667116
SN - 1463-9076
VL - 20
SP - 3403
EP - 3410
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 5
ER -