Susumu Aoyama, Ritsu Kamiya  Biophysical Journal 

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Cyclical Interactions between Two Outer Doublet Microtubules in Split Flagellar Axonemes  Susumu Aoyama, Ritsu Kamiya  Biophysical Journal  Volume 89, Issue 5, Pages 3261-3268 (November 2005) DOI: 10.1529/biophysj.105.067876 Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 1 Split axoneme obtained by protease/ATP treatment. Video-recorded dark-field micrograph. The axonemes tend to split into single outer doublets and bundles, while their proximal ends remain connected. Bar, 5μm. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 2 Cyclical interaction between a pair of outer doublet microtubules. A series of video frames taken every 10ms (see supplementary movie 1 (fourfold slowed down)). The number in each frame shows the time in milliseconds. This pair repeats an association/dissociation cycle at ∼9Hz. Note that no significant bending occurs in the associated portion. ATP concentration, 500μM. Bar, 5μm. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 3 Doublet pair showing a bending movement. Video frames taken every 30ms. This type of bending movement was frequently observed at lower ATP concentrations. ATP concentration, 5μM. Bar, 5μm. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 4 Change in the positions at which association (○; curve 1) and dissociation (●; curve 2) occurred between two doublet microtubules shown in Fig. 2. The doublet pair repeats association and dissociation at an almost constant frequency. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 5 Maximal velocities of the association/dissociation front progression at different ATP concentrations. (○) The association front. (●) The dissociation front. (Solid line) Data for the dissociation front fitted to Michaelis-Menten kinetics with the following parameters: maximal velocity=240μm/s; Km=107μM. For each data point, the average and standard deviation (error bars) measured in eight samples are shown. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 6 Pair of doublets displaying a distally traveling gap. Video frames taken every 5ms (see supplementary movie 2 (fourfold slowed down)). ATP concentration, 100μM. Bar, 5μm. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 7 Bend propagation in a microtubule bundle in a split axoneme. One of the two microtubule bundles in a split axoneme (left photo) is propagating a bend, as seen in the sequential photos shown right. Video frames taken every 5ms. ATP 100μM. Bar, 5μm. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 8 Model of the association/dissociation movement displayed by a doublet pair. (a) When two outer doublet microtubules are associated for a certain length, dynein (depicted by small projections on the right microtubule) generates sliding force. (b) The large bending moment at the base results in dissociation of the microtubules. (c and d) The dissociated portion spreads as the dissociation front moves toward the tip. (e) After complete dissociation, the two outer doublets start to reassociate at the base. The associated portion spreads as the association front moves toward the tip. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions

Figure 9 Model of wave propagation based on a “gap” movement. (A) Model for a traveling “gap” similar to that shown in Fig. 6. Simultaneous movements of the dissociation and association fronts (arrowheads) produce a distally traveling gap. (B) Model for bend propagation. If we assume that a gap is formed as in A but that the two outer doublets are connected by some loose structures, then interdoublet sliding will produce a bend (asterisk) that advances distally. Biophysical Journal 2005 89, 3261-3268DOI: (10.1529/biophysj.105.067876) Copyright © 2005 The Biophysical Society Terms and Conditions