Asymmetries in kinesin-2 and cytoplasmic dynein contributions to melanosome transport

被引:10
作者
Cecilia De Rossi, Maria [1 ]
Emilia De Rossi, Maria [2 ]
Sued, Mariela [3 ]
Rodriguez, Daniela [3 ]
Bruno, Luciana [4 ]
Levi, Valeria [1 ]
机构
[1] Univ Buenos Aires, Dept Quim Biol, Fac Ciencias Exactas & Nat, IQUIBICEN CONICET, RA-1428 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, CONICET, Inst Astron & Fis Espacio, RA-1428 Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, CONICET, Inst Calculo, RA-1428 Buenos Aires, DF, Argentina
[4] Univ Buenos Aires, Dept Fis, Fac Ciencias Exactas & Nat, IFIBA CONICET, RA-1428 Buenos Aires, DF, Argentina
来源
FEBS LETTERS | 2015年 / 589卷 / 19期
关键词
Single particle tracking; Molecular motors; Intracellular transport; Xenopus laevis melanophores; TUG-OF-WAR; XENOPUS-LAEVIS MELANOPHORES; PROTEIN-KINASE-A; MOLECULAR MOTORS; ORGANELLE TRANSPORT; MICROTUBULE MOTORS; LIVING CELLS; IN-VIVO; INTRACELLULAR-TRANSPORT; BIDIRECTIONAL TRANSPORT;
D O I
10.1016/j.febslet.2015.07.038
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanisms involved in bidirectional transport along microtubules remain largely unknown. We explored the collective action of kinesin-2 and dynein motors during transport of melanosomes in Xenopus laevis melanophores. These motors are attached to organelles through accessory proteins establishing a complex molecular linker. We determined both the stiffness of this linker and the organelles speed and observed that these parameters depended on the organelle size and cargo direction. Our results suggest that melanosome transport is driven by two dissimilar teams: whereas dynein motors compete with kinesin-2 affecting the properties of plus-end directed organelles, kinesin-2 does not seem to play a similar role during minus-end transport. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2763 / 2768
页数:6
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