Subsidiary Components of the Flagella of Chlamydomonas Reinhardii

1970 ◽  
Vol 7 (3) ◽  
pp. 823-839
Author(s):  
J. M. HOPKINS

Some subsidiary components of flagella from the alga Chlamydomonas reinhardii have been studied in the electron microscope using frayed and partially dispersed material, negatively stained. In all, 5 distinct subsidiary structures have been observed, 3 of which are associated with the 9 pairs of outer tubules and 2 with the central pair of tubules. 1. Radial spokes, about 33 nm long and 5 nm in diameter, are attached at right angles to the A tubule of each outer pair and extend into the lumen of the flagellum in the direction of the central pair of tubules, but do not reach them. The spokes usually occur in pairs along the length of each A tubule. The interval between pairs is about 70 nm and that between the 2 members of each pair about 30 nm. 2. ‘Secondary fibres’. The distal end of each spoke terminates in a hammerhead-like attachment some 10-20 nm by 5 nm with its axis parallel to the long axis of the flagellum. These hammerhead attachments are now identified with the so-called ‘secondary fibres’ previously deduced from micrographs of embedded and sectioned material. There is no evidence from the present work of a continuous secondary fibre throughout the length of the flagellum. 3. Side arms are found attached to the A tubule of each outer pair. These arms, which occur in pairs, are roughly at right angles to the radial spokes which are also attached to the A tubules. The side arm material is distributed along the tubule at regular intervals of about 14 nm. 4. The chemically more stable centre tubule has 2 longitudinal rows of projections, each projection being about 18 nm long with a repeat distance of about 16 nm. 5. Occasionally, on the chemically less stable centre tubule, there is observed one row of projections which are somewhat similar to those on the other tubule. New information has made it possible to reinterpret earlier work and to present a 3-dimensional picture of the external flagellum and its parts.

1999 ◽  
Vol 4 (S1) ◽  
pp. 852-857 ◽  
Author(s):  
H. Hirayama ◽  
Y. Aoyagi ◽  
S. Tanaka

We report on the first artificial fabrication of self-assembling AlGaN quantum dots (QDs) on AlGaN surfaces using metal organic chemical vapor deposition (MOCVD). The AlGaN QDs are fabricated using a growth mode change from 2-dimensional step-flow growth to 3-dimensional island formation by modifying the AlGaN surface energy with Si anti-surfactant. The average lateral size and the thickness of fabricated AlGaN QDs, as determined by AFM, are approximately 20 nm and 6nm, respectively. The dot density was found to be controlled from 5×1010 cm−2 down to 2×109 cm−2 by increasing the dose of Si anti-surfactant. We obtained the photoluminescence (PL) from AlGaN QDs embedded with Al0.38Ga0.62N capping layers. The Al incorporation in AlGaN QDs was controllable within the range of 1-5 %.


2004 ◽  
Vol 15 (12) ◽  
pp. 5431-5442 ◽  
Author(s):  
Triscia W. Hendrickson ◽  
Catherine A. Perrone ◽  
Paul Griffin ◽  
Kristin Wuichet ◽  
Joshua Mueller ◽  
...  

Increased phosphorylation of dynein IC IC138 correlates with decreases in flagellar microtubule sliding and phototaxis defects. To test the hypothesis that regulation of IC138 phosphorylation controls flagellar bending, we cloned the IC138 gene. IC138 encodes a novel protein with a calculated mass of 111 kDa and is predicted to form seven WD-repeats at the C terminus. IC138 maps near the BOP5 locus, and bop5-1 contains a point mutation resulting in a truncated IC138 lacking the C terminus, including the seventh WD-repeat. bop5-1 cells display wild-type flagellar beat frequency but swim slower than wild-type cells, suggesting that bop5-1 is altered in its ability to control flagellar waveform. Swimming speed is rescued in bop5-1 transformants containing the wild-type IC138, confirming that BOP5 encodes IC138. With the exception of the roadblock-related light chain, LC7b, all the other known components of the I1 complex, including the truncated IC138, are assembled in bop5-1 axonemes. Thus, the bop5-1 motility phenotype reveals a role for IC138 and LC7b in the control of flagellar bending. IC138 is hyperphosphorylated in paralyzed flagellar mutants lacking radial spoke and central pair components, further indicating a role for the radial spokes and central pair apparatus in control of IC138 phosphorylation and regulation of flagellar waveform.


1998 ◽  
Vol 537 ◽  
Author(s):  
H. Hirayama ◽  
Y Aoyagi ◽  
S. Tanaka

AbstractWe report on the first artificial fabrication of self-assembling AlGaN quantum dots (QDs) on AIGaN surfaces using metal organic chemical vapor deposition (MOCVD). The AlGaN QDs are fabricated using a growth mode change from 2-dimensional step-flow growth to 3-dimensional island formation by modifying the AlGaN surface energy with Si anti-surfactant. The average lateral size and the thickness of fabricated AlGaN QDs, as determined by AFM, are approximately 20 nm and 6nm, respectively. The dot density was found to be controlled from 5×1010cm-2 down to 2×109 cm-2 by increasing the dose of Si anti-surfactant. We obtained the photoluminescence (PL) from AlGaN QDs embedded with Al0.38Ga0.62N capping layers. The Al incorporation in AlGaN QDs was controllable within the range of 1-5 %.


2006 ◽  
Vol 6 (11) ◽  
pp. 3333-3337 ◽  
Author(s):  
Sangmin Shin ◽  
June-Mo Koo ◽  
Sukpil Kim ◽  
Bum-Seok Seo ◽  
Jung-Hyun Lee ◽  
...  

PbZrx Ti1−xO3 (PZT) thin films were deposited on 3-dimensional (3D) nano-scale trench structures for use in giga-bit density ferroelectric random access memories. PZT thin films were deposited by liquid delivery metalorganic chemical vapor deposition using Pb(thd)2, Zr(MMP)4, and Ti(MMP)4 precursors dissolved in ethyl cyclohexane. Iridium thin films were deposited by atomic layer deposition, and they exhibited excellent properties for capacitor electrodes even at a thickness of 20 nm. The trench capacitor was composed of three layers, viz. Ir/PZT/Ir (20/60/20 nm), and had a diameter of 250 nm and a height of 400 nm. Almost 100% step coverage was obtained at a deposition temperature of 530 °C. The PZT thin film capacitors with a thickness of 60 nm on a planar structure exhibited a remnant polarization (Pr of 28 μC/cm2, but the Pr value of the 3D PZT capacitors decreased slightly with decreasing 3D trench pattern size. The transmission electron microscope analysis indicated that the PZT thin films had compositional uniformity in the 3D trench region. Both columnar and granular grains were formed on the sidewalls of the trench capacitors, and their relative proportion exhibited strong size dependence. The trench capacitors with more columnar PZT grains showed good switching behavior under an external bias of 2.1 V and had a remnant polarization of 19 ∼ 24 μC/cm2.


Author(s):  
SÁNDOR R. FEKETE ◽  
HENK MEIJER

We discuss rectangle and box visibility representations of graphs in 3-dimensional space. In these representations, vertices are represented by axis-aligned disjoint rectangles or boxes. Two vertices are adjacent if and only if their corresponding boxes see each other along a small axis-parallel cylinder. We concentrate on lower and upper bounds for the size of the largest complete graph that can be represented. In particular, we examine these bounds under certain restrictions: What can be said if we may only use boxes of a limited number of shapes? Some of the results presented are as follows: • There is a representation of K8 by unit boxes. • There is no representation of K10 by unit boxes. • There is a representation of K56, using 6 different box shapes. • There is no representation of K184 by general boxes. A special case arises for rectangle visibility graphs, where no two boxes can see each other in the x- or y-directions, which means that the boxes have to see each other in z-parallel direction. This special case has been considered before; we give further results, dealing with the aspects arising from limits on the number of shapes.


2006 ◽  
Vol 115 ◽  
pp. 275-278 ◽  
Author(s):  
V.I. Mitrokhin ◽  
S.I. Rembeza ◽  
E.S. Rembeza ◽  
A.A. Rudenko

Internal friction results obtained in thin SnO2 films produced by reactive magnetron sputtering (thickness of the film ~ 1 μm) and by the dehydration of water solution of tin salts (thickness of the film ~ 10 μm) are reported. It is suggested that internal friction peak observed in SnO2 films at around 170 oC is caused by relaxation processes on grain boundaries (average grain size is 20 nm). The investigation of internal friction in SnO2 films can yield new information about the structure of thin films.


1987 ◽  
Vol 105 (3) ◽  
pp. 1297-1301 ◽  
Author(s):  
Y Hosokawa ◽  
T Miki-Noumura

Relatively little is known about the functions of central-pair microtubules (Tamm, S. L., and G. A. Horridge, 1970, Proc. Roy. Soc. Lond. B, 175: 219-233; Omoto, C. K., and C. Kung, 1979, Nature (Lond.). 279:532-534) and radial spokes (Warner, F. D., and P. Satir, 1974, J. Cell Biol., 63:35-63), although a sliding microtubule mechanism has been established for the flagellar movement (Summers, K. E., and I. R. Gibbons, 1971, Proc. Natl. Acad. Sci. USA., 68:3092-3096). In the present report, an attempt was made to determine the functions of central-pair microtubules in flagellar motility. Central-pair microtubules were found to extrude from the tips of elastase-digested axonemes of demembranated Chlamydomonas flagella after the addition of ATP. The length of the extruded central-pair microtubules was approximately 70-100% that of the axoneme. After extrusion, axonemes continued to swim slowly backwards in the reactivation medium, with a trailing central pair attached like a tail to the flagellar tip. During bending movement of the axonemes, partially extruded central pairs rotated counterclockwise about the axoneme axis, as viewed from the distal end (Kamiya, R., 1982, Cell Motil. [Suppl.]:169-173). Axonemes swam backwards with a symmetric waveform and a beat frequency of approximately 10 Hz in the reactivation medium containing 10(-9)-10(-4) M Ca ions. Even at a lower Ca++ concentration, no ciliary-type swimming was noted on the axonemes.


2017 ◽  
Vol 474 (9) ◽  
pp. 1467-1479 ◽  
Author(s):  
Thorsten Maretzky ◽  
Steven Swendeman ◽  
Elin Mogollon ◽  
Gisela Weskamp ◽  
Umut Sahin ◽  
...  

ADAM9 (A Disintegrin And Metalloprotease 9) is a membrane-anchored metalloproteinase that has been implicated in pathological retinal neovascularization and in tumor progression. ADAM9 has constitutive catalytic activity in both biochemical and cell-based assays and can cleave several membrane proteins, including epidermal growth factor and Ephrin receptor B4; yet little is currently known about the catalytic properties of ADAM9 and its post-translational regulation and inhibitor profile in cell-based assays. To address this question, we monitored processing of the membrane-anchored Ephrin receptor B4 (EphB4) by co-expressing ADAM9, with the catalytically inactive ADAM9 E > A mutant serving as a negative control. We found that ADAM9-dependent shedding of EphB4 was not stimulated by three commonly employed activators of ADAM-dependent ectodomain shedding: phorbol esters, pervanadate or calcium ionophores. With respect to the inhibitor profile, we found that ADAM9 was inhibited by the hydroxamate-based metalloprotease inhibitors marimastat, TAPI-2, BB94, GM6001 and GW280264X, and by 10 nM of the tissue inhibitor of metalloproteinases (TIMP)-3, but not by up to 20 nM of TIMP-1 or -2. Additionally, we screened a non-hydroxamate small-molecule library for novel ADAM9 inhibitors and identified four compounds that selectively inhibited ADAM9-dependent proteolysis over ADAM10- or ADAM17-dependent processing. Taken together, the present study provides new information about the molecular fingerprint of ADAM9 in cell-based assays by showing that it is not stimulated by strong activators of ectodomain shedding and by defining a characteristic inhibitor profile. The identification of novel non-hydroxamate inhibitors of ADAM9 could provide the basis for designing more selective compounds that block the contribution of ADAM9 to pathological neovascularization and cancer.


1990 ◽  
Vol 147 ◽  
pp. 5-43
Author(s):  
R.K Pickerill ◽  
J.S Peel

New trace fossil collections are described from Lower Cambrian siliciclastic shallow marine shelf deposits of the Bastion Formation of North-East Greenland, together with a taxonomic re-assessment of previously reported material. The entire assemblage comprises 19 ichnogenera, 25 ichnospecies, as well as two vernacular ichnotaxa. Although no new ichnotaxa are present the material reveals new information on the 3-dimensional structure of two of the contained ichnogenera, namely Plagiogmus Roedel and Psammichnites TorelI. The stratigraphic range of a single ichnospecies, Rusophycus latus Webby, is formally extended from the Lower Ordovician to the Lower Cambrian. The assemblage compares favourably with Lower Cambrian ichnocoenoses described from other continents, particularly at the ichnogeneric level. Comparison with similar sequences suggests that the sub-trilobitic Lower Bastion Formation is late Tommotian to early Atdabanian in age, possibly entirely Atdabanian.


2008 ◽  
Vol 180 (3) ◽  
pp. 633-643 ◽  
Author(s):  
Karl-Ferdinand Lechtreck ◽  
Philippe Delmotte ◽  
Michael L. Robinson ◽  
Michael J. Sanderson ◽  
George B. Witman

Chlamydomonas reinhardtii hydin is a central pair protein required for flagellar motility, and mice with Hydin defects develop lethal hydrocephalus. To determine if defects in Hydin cause hydrocephalus through a mechanism involving cilia, we compared the morphology, ultrastructure, and activity of cilia in wild-type and hydin mutant mice strains. The length and density of cilia in the brains of mutant animals is normal. The ciliary axoneme is normal with respect to the 9 + 2 microtubules, dynein arms, and radial spokes but one of the two central microtubules lacks a specific projection. The hydin mutant cilia are unable to bend normally, ciliary beat frequency is reduced, and the cilia tend to stall. As a result, these cilia are incapable of generating fluid flow. Similar defects are observed for cilia in trachea. We conclude that hydrocephalus in hydin mutants is caused by a central pair defect impairing ciliary motility and fluid transport in the brain.


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