Single fungal kinesin motor molecules move processively along Microtubules

被引:28
作者
Lakämper, S
Kallipolitou, A
Woehlke, G
Schliwa, M
Meyhöfer, E [1 ]
机构
[1] Hannover Med Sch, D-30635 Hannover, Germany
[2] Univ Munich, Abolf Butenandt Inst Cell Biol, D-80336 Munich, Germany
[3] Univ Michigan, Ann Arbor, MI 48109 USA
关键词
D O I
10.1016/S0006-3495(03)74991-1
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Conventional kinesins are two-headed molecular motors that move as single molecules micrometer-long distances on microtubules by using energy derived from ATP hydrolysis. The presence of two heads is a prerequisite for this processive motility, but other interacting domains, like the neck and K-loop, influence the processivity and are implicated in allowing some single-headed kinesins to move processively. Neurospora kinesin (NKin) is a phylogenetically distant, dimeric kinesin from Neurospora crassa with high gliding speed and an unusual neck domain. We quantified the processivity of NKin and compared it to human kinesin, HKin, using gliding and fluorescence-based processivity assays. Our data show that NKin is a processive motor. Single NKin molecules translocated microtubules in gliding assays on average 2.14 mum (N = 46). When we tracked single, fluorescently labeled NKin motors, they moved on average 1.75 Am (N = 182) before detaching from the microtubule, whereas HKin motors moved shorter distances (0.83 mum, N = 229) under identical conditions. NKin is therefore at least twice as processive as HKin. These studies, together with biochemical work, provide a basis for experiments to dissect the molecular mechanisms of processive movement.
引用
收藏
页码:1833 / 1843
页数:11
相关论文
共 71 条
[1]  
Becker R. A., 1988, NEW S LANGUAGE
[2]   BEAD MOVEMENT BY SINGLE KINESIN MOLECULES STUDIED WITH OPTICAL TWEEZERS [J].
BLOCK, SM ;
GOLDSTEIN, LSB ;
SCHNAPP, BJ .
NATURE, 1990, 348 (6299) :348-352
[3]   NATIVE STRUCTURE AND PHYSICAL-PROPERTIES OF BOVINE BRAIN KINESIN AND IDENTIFICATION OF THE ATP-BINDING SUBUNIT POLYPEPTIDE [J].
BLOOM, GS ;
WAGNER, MC ;
PFISTER, KK ;
BRADY, ST .
BIOCHEMISTRY, 1988, 27 (09) :3409-3416
[4]   A NOVEL BRAIN ATPASE WITH PROPERTIES EXPECTED FOR THE FAST AXONAL-TRANSPORT MOTOR [J].
BRADY, ST .
NATURE, 1985, 317 (6032) :73-75
[5]   Kinesin's tail domain is an inhibitory regulator of the motor domain [J].
Coy, DL ;
Hancock, WO ;
Wagenbach, M ;
Howard, J .
NATURE CELL BIOLOGY, 1999, 1 (05) :288-292
[6]   Kinesin takes one 8-nm step for each ATP that it hydrolyzes [J].
Coy, DL ;
Wagenbach, M ;
Howard, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) :3667-3671
[7]   Coupled chemical and mechanical reaction steps in a processive Neurospora kinesin [J].
Crevel, I ;
Carter, N ;
Schliwa, M ;
Cross, R .
EMBO JOURNAL, 1999, 18 (21) :5863-5872
[8]   Kinetic evidence for low chemical processivity in ncd and Eg5 [J].
Crevel, IMTC ;
Lockhart, A ;
Cross, RA .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 273 (01) :160-170
[9]   EVIDENCE THAT THE STALK OF DROSOPHILA KINESIN HEAVY-CHAIN IS AN ALPHA-HELICAL COILED COIL [J].
DECUEVAS, M ;
TAO, T ;
GOLDSTEIN, LSB .
JOURNAL OF CELL BIOLOGY, 1992, 116 (04) :957-965
[10]   Kinetic studies of dimeric Ncd: Evidence that Ncd is not processive [J].
Foster, KA ;
Gilbert, SP .
BIOCHEMISTRY, 2000, 39 (07) :1784-1791