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2.
J Cell Biol ; 151(5): 1081-92, 2000 Nov 27.
Article in English | MEDLINE | ID: mdl-11086009

ABSTRACT

Conventional kinesin, a dimeric molecular motor, uses ATP-dependent conformational changes to move unidirectionally along a row of tubulin subunits on a microtubule. Two models have been advanced for the major structural change underlying kinesin motility: the first involves an unzippering/zippering of a small peptide (neck linker) from the motor catalytic core and the second proposes an unwinding/rewinding of the adjacent coiled-coil (neck coiled-coil). Here, we have tested these models using disulfide cross-linking of cysteines engineered into recombinant kinesin motors. When the neck linker motion was prevented by cross-linking, kinesin ceased unidirectional movement and only showed brief one-dimensional diffusion along microtubules. Motility fully recovered upon adding reducing agents to reverse the cross-link. When the neck linker motion was partially restrained, single kinesin motors showed biased diffusion towards the microtubule plus end but could not move effectively against a load imposed by an optical trap. Thus, partial movement of the neck linker suffices for directionality but not for normal processivity or force generation. In contrast, preventing neck coiled-coil unwinding by disulfide cross-linking had relatively little effect on motor activity, although the average run length of single kinesin molecules decreased by 30-50%. These studies indicate that conformational changes in the neck linker, not in the neck coiled-coil, drive processive movement by the kinesin motor.


Subject(s)
Disulfides/metabolism , Kinesins/chemistry , Kinesins/metabolism , Molecular Motor Proteins/chemistry , Molecular Motor Proteins/metabolism , Cross-Linking Reagents/chemistry , Cross-Linking Reagents/metabolism , Diffusion , Dimerization , Humans , Kinesins/genetics , Microtubules/metabolism , Molecular Motor Proteins/genetics , Mutagenesis/physiology , Protein Structure, Secondary/physiology
3.
Spine (Phila Pa 1976) ; 25(10): 1290-2, 2000 May 15.
Article in English | MEDLINE | ID: mdl-10806509

ABSTRACT

STUDY DESIGN: Case report. OBJECTIVES: Successful excision of the exostosis within the spinal canal. SUMMARY OF BACKGROUND DATA: Myelopathy caused by exostosis within the spinal canal developed in a 13-year-old boy with hereditary multiple exostosis. METHODS: Spinous process-splitting laminoplasty with an ultrasonic knife was performed to remove the mass and minimize the possibility of postlaminectomy kyphosis. RESULTS: The spinal canal exostosis with cervical cord compression was excised successfully with laminoplasty. After surgery there has been no recurrence of tumor, and the stability of the cervical spine has been preserved. CONCLUSION: This is the first report of laminoplasty as a useful surgical approach for intraspinal exostosis to prevent postoperative cervical instability.


Subject(s)
Exostoses, Multiple Hereditary/surgery , Laminectomy/methods , Osteochondroma/surgery , Spinal Cord Compression/surgery , Spinal Cord Neoplasms/surgery , Adolescent , Exostoses, Multiple Hereditary/diagnostic imaging , Humans , Joint Instability/diagnostic imaging , Joint Instability/surgery , Male , Osteochondroma/diagnostic imaging , Spinal Cord Compression/diagnostic imaging , Spinal Cord Neoplasms/diagnostic imaging , Tomography, X-Ray Computed
5.
J Cell Biol ; 142(4): 989-1000, 1998 Aug 24.
Article in English | MEDLINE | ID: mdl-9722611

ABSTRACT

Mechanisms that regulate the movement of a membrane spanning protein band 3 in erythrocyte ghosts were investigated at the level of a single or small groups of molecules using single particle tracking with an enhanced time resolution (0.22 ms). Two-thirds of band 3 undergo macroscopic diffusion: a band 3 molecule is temporarily corralled in a mesh of 110 nm in diameter, and hops to an adjacent mesh an average of every 350 ms. The rest (one-third) of band 3 exhibited oscillatory motion similar to that of spectrin, suggesting that these band 3 molecules are bound to spectrin. When the membrane skeletal network was dragged and deformed/translated using optical tweezers, band 3 molecules that were undergoing hop diffusion were displaced toward the same direction as the skeleton. Mild trypsin treatment of ghosts, which cleaves off the cytoplasmic portion of band 3 without affecting spectrin, actin, and protein 4.1, increased the intercompartmental hop rate of band 3 by a factor of 6, whereas it did not change the corral size and the microscopic diffusion rate within a corral. These results indicate that the cytoplasmic portion of band 3 collides with the membrane skeleton, which causes temporal confinement of band 3 inside a mesh of the membrane skeleton.


Subject(s)
Cell Membrane/metabolism , Erythrocytes/physiology , Anion Exchange Protein 1, Erythrocyte/metabolism , Cytoskeleton/physiology , Diffusion , Erythrocyte Membrane/chemistry , Gold Colloid/metabolism , Humans , Membrane Proteins/metabolism , Microscopy, Video , Spectrin/metabolism , Trypsin/pharmacology
8.
Seikei Geka ; 23(2): 121, 1972 Feb.
Article in Japanese | MEDLINE | ID: mdl-5062463

Subject(s)
Surgical Equipment
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