Mechanics of motility: distinct dynein binding domains on α- and β-tubulin

1995 ◽  
Vol 73 (9-10) ◽  
pp. 665-671 ◽  
Author(s):  
Matthew Goldsmith ◽  
Derek van der Kooy ◽  
Lynwood Yarbrough
Keyword(s):  
Sperm Motility ◽  
Sea Urchin ◽  
Particle Transport ◽  
Binding Domain ◽  
Motility Assay ◽  
Flagellar Motility ◽  
Binding Domains ◽  
Tubulin Binding ◽  
Sea Urchin Sperm ◽  
Β Tubulin

Microtubules (MTs) interact with force-generating proteins to generate a variety of intracellular movements, including intracellular particle transport, ciliary–flagellar beating, and chromosome–spindle movements during mitosis–meiosis. Relatively little is known about the mechanics of these motor-MT interactions, in part because the motor binding domains of the MT and the corresponding MT binding domains of the motor have not been well characterized. Using a flagellar motility assay, we report that the MT subunits, α- and β-tubulin, each contain a dynein binding domain located near the C-termini of their respective tubulin subunits. Blocking either α- or β-tubulin binding domains of dynein attenuates motility in demembranated sea urchin sperm up to 50%. Interestingly, blocking both α- and β-tubulin binding domains on dynein produces much greater decreases in motility. These data suggest that flagellar dynein binds to both subunits of the MT polymer, α- and β-tubulin. In addition, the two subunits appear to contribute equivalent, but functionally separate, roles to flagellar motility.Key words: microtubule, microtubule-based motility, dynein, sperm motility.

Crosstalk between protein kinases A and C regulates sea urchin sperm motility

Zygote ◽  
2021 ◽  
pp. 1-12
Author(s):  
Arlet Loza-Huerta ◽  
Hiram Pacheco-Castillo ◽  
Alberto Darszon ◽  
Carmen Beltrán
Keyword(s):  
Protein Kinase ◽  
Sperm Motility ◽  
Sea Urchin ◽  
Sea Urchins ◽  
Dependent Protein Kinase ◽  
Kinase C ◽  
Competitive Inhibitors ◽  
Motility Regulation ◽  
Dependent Protein ◽  
Sea Urchin Sperm

Summary Fertilization, a crucial event for species preservation, in sea urchins, as in many other organisms, requires sperm motility regulation. In Strongylocentrotus purpuratus sea urchins, speract, a sperm chemoattractant component released to seawater from the outer egg layer, attracts sperm after binding to its receptor in the sperm flagellum. Previous experiments performed in demembranated sperm indicated that motility regulation in these cells involved protein phosphorylation mainly due to the cAMP-dependent protein kinase (PKA). However, little information is known about the involvement of protein kinase C (PKC) in this process. In this work, using intact S. purpuratus sea urchin sperm, we show that: (i) the levels of both phosphorylated PKA (PKA substrates) and PKC (PKC substrates) substrates change between immotile, motile and speract-stimulated sperm, and (ii) the non-competitive PKA (H89) and PKC (chelerythrine) inhibitors diminish the circular velocity of sperm and alter the phosphorylation levels of PKA substrates and PKC substrates, while the competitive inhibitors Rp-cAMP and bisindolylmaleimide (BIM) do not. Altogether, our results show that both PKA and PKC participate in sperm motility regulation through a crosstalk in the signalling pathway. These results contribute to a better understanding of the mechanisms that govern motility in sea urchin sperm.

scholarly journals Inhibition of movement of trition-demembranated sea-urchin sperm flagella by Mg2+, ATP4-, ADP and P1

1979 ◽  
Vol 38 (1) ◽  
pp. 105-123
Author(s):  
M. Okuno ◽  
C.J. Brokaw
Keyword(s):  
Sea Urchin ◽  
Glass Surface ◽  
Beat Frequency ◽  
Bend Angle ◽  
Flagellar Motility ◽  
Reaction Products ◽  
Inhibitory Effects ◽  
Linear Relationships ◽  
Clinical Patterns ◽  
Sea Urchin Sperm

Three clinical patterns of inhibition of MgATP2—activated flagellar motility have been found by measuring the motility of Triton-demembranated sea-urchin spermatozoa beating with their heads attached to a glass surface. Inhibition of beat frequency by the reaction products, ADP and Pi, is competitive with the normal substrate, MgATP2-, and the inhibitory effects are similar to a reduction in MgATP2- concentration. Inhibition of beat frequency by ATP4- is competitive with MgATP2, but is accompanied by an inhibition of bending, as measured by the angle between the straight regions on either side of a bend, which is not seen when MgATP2- concentration is reduced. Inhibition of beat frequency by Mg2+ is not competitive with MgATP2-, and is accompanied by an increase in bend angle, so that there is no change in the rate of sliding between flagellar tubules. These differences suggest unexpected complexity of dynein ATPase action in flagella. The beat frequencies of both swimming and attached spermatozoa show a linear double reciprocal dependence on MgATP2- concentration, with identical slopes. The calculated sliding velocities between tubules also give linear relationships, but the slopes are different, suggesting that beat frequency may be the more fundamental dependent variable in this system.

The polyglutamylated lateral chain of alpha-tubulin plays a key role in flagellar motility

1996 ◽  
Vol 109 (6) ◽  
pp. 1545-1553 ◽  
Author(s):  
C. Gagnon ◽  
D. White ◽  
J. Cosson ◽  
P. Huitorel ◽  
B. Edde ◽  
...  
Keyword(s):  
Sea Urchin ◽  
Beat Frequency ◽  
Cortical Microtubule ◽  
Flagellar Motility ◽  
Microtubule Network ◽  
Alpha Tubulin ◽  
Oxyrrhis Marina ◽  
Terminal Domain ◽  
Flagellar Beat ◽  
Sea Urchin Sperm

To investigate whether a specific isotype of tubulin is involved in flagellar motility, we have developed and screened a panel of monoclonal antibodies (mAb) generated against sea urchin sperm axonemal proteins. Antibodies were selected for their ability to block the motility of permeabilized sperm models. The antitubulin mAb B3 completely inhibited, at low concentrations, the flagellar motility of permeabilized sperm models from four sea urchin species. On immunoblots, B3 recognized predominantly alpha-tubulin in sea urchin sperm axonemes and equally well brain alpha- and beta-tubulins. Subtilisin cleavage of tubulin removed the B3 epitope, indicating that it was restricted to the last 13 amino acid residues of the C-terminal domain of alpha-tubulin. In enzyme-linked immunosorbant assays, B3 reacted with glutamylated alpha-tubulin peptides from sea urchin or mouse brain but did not bind to the unmodified corresponding peptide, indicating that it recognized polyglutamylated motifs in the C-terminal domain of alpha-tubulin. On the other hand, other tubulin antibodies directed against various epitopes of the C-terminal domain, with the exception of the antipolyglutamylated mAb GT335, had no effect on motility while having binding properties similar to that of B3. B3 and GT335 acted by decreasing the beating amplitude without affecting the flagellar beat frequency. B3 and GT335 were also capable of inhibiting the motility of flagella of Oxyrrhis marina, a 400,000,000 year old species of dinoflagellate, and those of human sperm models. Localization of the antigens recognized by B3 and GT335 by immunofluorescence techniques revealed their presence along the whole axoneme of sea urchin spermatozoa and flagella of O. marina, except for the distal tip and the cortical microtubule network of the dinoflagellate. Taken together, the data reported here indicate that the polyglutamylated lateral chain of alpha-tubulin plays a dynamic role in a dynein-based motility process.

Conserved ?-tubulin binding domain for the microtubule-associated motors underlying sperm motility and fast axonal transport

1991 ◽  
Vol 20 (3) ◽  
pp. 249-262 ◽  
Author(s):  
Matthew Goldsmith ◽  
Joe A. Connolly ◽  
Norm Kumar ◽  
Jie Wu ◽  
Lynwood R. Yarbrough ◽  
...  
Keyword(s):  
Axonal Transport ◽  
Sperm Motility ◽  
Binding Domain ◽  
Fast Axonal Transport ◽  
Tubulin Binding

scholarly journals Network model predicts that CatSper is the main Ca2+ channel in the regulation of sea urchin sperm motility

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Jesús Espinal-Enríquez ◽  
Daniel Alejandro Priego-Espinosa ◽  
Alberto Darszon ◽  
Carmen Beltrán ◽  
Gustavo Martínez-Mekler
Keyword(s):  
Sperm Motility ◽  
Sea Urchin ◽  
Network Model ◽  
Sea Urchin Sperm

scholarly journals Altering the speract-induced ion permeability changes that generate flagellar Ca2+ spikes regulates their kinetics and sea urchin sperm motility

2007 ◽  
Vol 306 (2) ◽  
pp. 525-537 ◽  
Author(s):  
Christopher D. Wood ◽  
Takuya Nishigaki ◽  
Yoshiro Tatsu ◽  
Noboru Yumoto ◽  
Shoji A. Baba ◽  
...  
Keyword(s):  
Sperm Motility ◽  
Sea Urchin ◽  
Ion Permeability ◽  
Permeability Changes ◽  
Sea Urchin Sperm

scholarly journals Effects of adenylyl imidodiphosphate, a nonhydrolyzable adenosine triphosphate analog, on reactivated and rigor wave sea urchin sperm.

1978 ◽  
Vol 79 (3) ◽  
pp. 827-832 ◽  
Author(s):  
S M Penningroth ◽  
G B Witman
Keyword(s):  
Adenosine Triphosphate ◽  
Sea Urchin ◽  
Beat Frequency ◽  
Atp Binding ◽  
Flagellar Motility ◽  
Lytechinus Pictus ◽  
Cross Bridge ◽  
Atp Concentration ◽  
Sea Urchin Sperm

A nonhydrolyzable ATP analog, adenylyl imidodiphosphate (AMP-PNP), has been used to study the role of ATP binding in flagellar motility. Sea urchin sperm of Lytechinus pictus were demembranated, reactivated, and locked in "rigor waves" by a modification of the method of Gibbons and Gibbons (11). Rigor wave sperm relaxed within 2 min after addition of 4 micrometer ATP, and reactivated upon addition of 10-12 micrometer ATP. The beat frequency of the reactivated sperm varied with ATP concentration according to Michaelis-Menten kinetics ("Km" = 0.24 mM; "Vmax" = 44 Hz) and was competitively inhibited by AMP-PNP (Ki" approximately to 8.1 mM). Rigor wave sperm were completely relaxed (straightened) within 2 min by AMP-PNP at concentrations of 2-4 mM. The possibilities that relaxation in AMP-PNP was a result of ATP contamination, AMP-PNP hydrolysis, or lowering of the free Mg++ concentration were conclusively ruled out. The results suggest that dynein cross-bridge release is dependent upon ATP binding but not hydrolysis.

scholarly journals Single cell neuro-sensory dynamics: Ca2+chemoreceptor-guided sea urchin sperm motility

2013 ◽  
Vol 14 (S1) ◽  
Author(s):  
J Nathan Kutz ◽  
Lisa J Burton ◽  
Yasmeen Hussain ◽  
Jeff Riffell ◽  
Jeffrey S Guasto ◽  
...  
Keyword(s):  
Single Cell ◽  
Sperm Motility ◽  
Sea Urchin ◽  
Sea Urchin Sperm

scholarly journals Molecular Cloning and Characterization of a Radial Spoke Head Protein of Sea Urchin Sperm Axonemes: Involvement of the Protein in the Regulation of Sperm Motility

1998 ◽  
Vol 9 (2) ◽  
pp. 513-522 ◽  
Author(s):  
Denis Gingras ◽  
Daniel White ◽  
Jérome Garin ◽  
Jacky Cosson ◽  
Philippe Huitorel ◽  
...  
Keyword(s):  
Sea Urchin ◽  
Beat Frequency ◽  
Three Dimensional ◽  
Coiled Coil ◽  
Structural Features ◽  
Flagellar Motility ◽  
Native Form ◽  
Radial Spoke ◽  
Single Polypeptide ◽  
Sea Urchin Sperm

Monoclonal antibodies raised against axonemal proteins of sea urchin spermatozoa have been used to study regulatory mechanisms involved in flagellar motility. Here, we report that one of these antibodies, monoclonal antibody D-316, has an unusual perturbating effect on the motility of sea urchin sperm models; it does not affect the beat frequency, the amplitude of beating or the percentage of motile sperm models, but instead promotes a marked transformation of the flagellar beating pattern which changes from a two-dimensional to a three-dimensional type of movement. On immunoblots of axonemal proteins separated by SDS-PAGE, D-316 recognized a single polypeptide of 90 kDa. This protein was purified following its extraction by exposure of axonemes to a brief heat treatment at 40°C. The protein copurified and coimmunoprecipitated with proteins of 43 and 34 kDa, suggesting that it exists as a complex in its native form. Using D-316 as a probe, a full-length cDNA clone encoding the 90-kDa protein was obtained from a sea urchin cDNA library. The sequence predicts a highly acidic (pI = 4.0) protein of 552 amino acids with a mass of 62,720 Da (p63). Comparison with protein sequences in databases indicated that the protein is related to radial spoke proteins 4 and 6 (RSP4 and RSP6) of Chlamydomonas reinhardtii, which share 37% and 25% similarity, respectively, with p63. However, the sea urchin protein possesses structural features distinct from RSP4 and RSP6, such as the presence of three major acidic stretches which contains 25, 17, and 12 aspartate and glutamate residues of 34-, 22-, and 14-amino acid long stretches, respectively, that are predicted to form α-helical coiled-coil secondary structures. These results suggest a major role for p63 in the maintenance of a planar form of sperm flagellar beating and provide new tools to study the function of radial spoke heads in more evolved species.

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