S U P P L E M E N TA R Y I N F O R M AT I O N DOI:.38/ncb363 Supplementary Figure Mean Residue Elipticity (deg cm / dmol) *^-3-5 7HPSHUDWXUH Û& 4 6 8 - -5 - CC melting -5 CC cooling -3 CCB cooling CCB melting -35-4 -45 Supplementary Figure Temperature dependent melting and reannealing of p5glued CC and CCB fragments. Molar ellipticity of CC and CCB at nm was monitored under increasing and decreasing temperature. Unfolding was reversible. Tm values were 3.5 C for CCB and 33 C for CC. (One independent experiment). WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
Supplementary Figure A Bead Position (m) B. -.3 -.6 -.9 -. Time(sec) -.5 4 6 8 - - 3 Bead Position (m) Single Dynein Force. -.3 -.6 - Time (s) -.9 4 6 8-4 6 Bead Position (m). -.3 -.6 -.9 Force(pN) Single Dynein Force - -. 3 4 5 6-3 4 C - 44.7 45. 45.3 45.6 Single p5-555-dynein - 5.8 6. 6.4 6.7 7. Single p5-555-dynein D MSD (m /sec) -.8.4 7. 7.4 7.7 p5-555 Alone (D) MSD Fit (D t + v t ) D =.69 m /sec....4.6 E MSD (m ) - 8.8 9. 9.4 9.7 3..3.5 CCA-dynein (D) MSD Fit (D t + v t ) D =.8 m /sec....4.6 F MSD (m /sec).7.35. p5-555-dynein (D) p5-555-dynein (P) MSD Fit (D t + v t ) D =.4 m /sec...4.6 P D v =. m/sec G MSD (m /sec).6.4. p35-cc-dynein (P) p35-cc-dynein (D) MSD Fit (D t + v t ) v =.33 m/sec. D =. m /sec...4.6 P D Supplementary Figure Additional examples of force traces and MSD curves. (A) Video trace showing measurement of single dynein force followed by its run-length. Blue star marks force production, red arrow indicates turning off of optical trap, and blue arrow shows end of runlength (B) and (C): Force traces from dynein alone and with P5. Experiments were done at a bead binding fraction of 3%. (D): The MSD curve for beads with P5 alone (3% binding fraction) diffusing along microtubules. (E) The MSD curve for single-molecule dynein beads (3% bf) with CCA, diffusing along MTs. (F, G): MSD curves for dynein (again 3% bf) with P5 (E) and P35 (F). The blue curves reflect the diffusing beads, whereas the red curves reflect the processively moving beads. WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
A B E - Bead in Trap, No MT Binding - 5 5 C F H I J - - 5 5 - - 5 5 - Single p5-555 Single p5-555 - Dynein Single p35-cc-dynein - 3.6.8. -.8 -.6.6.8. -.8 -.6.6.8. -.8 -.6 Single p5-555 Fitting 6 8 Single p5-555 - Dynein Fitting 4 5 6 7 Single p35-cc-dynein Fitting 3 Normalized Count *Standard Deviation =.5 pn 5 5 -. -.5..5. D G Normalized Counts Normalized Count 8 6 4 Normalized Count -. -.5..5. 4 3 Single p5-555-dynein Fit.35. pn.36. pn -. -.5..5. 8 6 4 Single p5-555 Gauss Fit Single p35-cc-dynein Fit -.53.4 pn.49.3 pn -. -.5..5. Supplementary Figure 3 Measurement of force distribution for diffusive beads. (A) (left):force trace of free bead, held in trap. The quadrant photo diode (QPD) signal was obtained at 4 KHz, with trap stiffness of.5 pn/nm. (right):histogram of detected forces due to thermal motion for the free bead (B) Force trace for bead attached to microtubule by a single p5-555 without dynein. (C) Higher temporal resolution image of (B). (D) Distribution of displacements (from fits in (B)) from many traces (475 force events). (E, F, and G (775 force events ) Same as (A, B and C) for, dynein with p5-555. (H, I and J (58 force events)) Same as (A, B and C) for dynein with p35-cc. In all cases, the QPD signal was averaged to KHz and analyzed using Kerssemakers step detection algorithm, with waiting time restricted to 5 ms. While (D) is described by a single Gaussian (no additional force production), (G) and (J) each require the sum of three Gaussian peaks. The small peaks indicate the presence of some force. We interpret these small forces as likely reflecting transient binding/ release events by dynein (see supplemental discussion). WWW.NATURE.COM/NATURECELLBIOLOGY 3 4 Macmillan Publishers Limited. All rights reserved.
A Position (nm) 8 96 8 64 48 3 6 Kinesin-EXPT Detected Steps AOD Feedback -6....3 Counts (Normalized).5..5 Position (nm) 96 8 64 48 3 EXPT_Kinesin Sim_With Backsteps Residual. -3-6 6 3 48 Step Size (nm) Kinesin Simulation Detected Steps 6... C D E F Position (nm) Counts (Normalized) Supplementary Figure 4..5. Counts (Normalized).5 6 44 8 Dynein Sim (+8nm) Detected Steps 96 8 64 48 3 6....3.6.4.. EXPT_Kinesin Sim_+8nm only Residual -3-6 6 3 48 Step Size (nm) EXPT_Dyn Simulation Residual -3-6 6 3 48 Step Size (nm) G Counts (Normalized)..9.6.3. B EXPT_Dyn Simulation (+8 nm only) -3-6 6 3 48 Step Size (nm) I J K L Stepping Probability Ratio Position (nm) 76 6 44 8 96 8 64 48 6 3 (CCB-Dynein):Dynein Ratio = -4-6 -8 8 6 4 3 Step Size (nm) CCB-Dynein Sim Step Detection -6....3 M Normalized Counts Integrated Residuals.3.. With Back Steps No Back Steps. -3-6 6 3 48 Step Size (nm) 96 8 64 48 3 6 Position (nm) Counts (Normalized) H.6.4.. Detected Steps From Video Traces Dynein CCB-Dynein Dynein Simulation Step Detection... EXPT_CCB-Dyn Simulation Residual -48-3 -6 6 3 48 64 Step Sizes -3-6 6 3 48 Step Size (nm) Supplementary Figure 4 Characterization of step detection. Step sizes were measured with an optical trap and an acousto optic deflector (AOD) force feedback system on single-motor (3% binding fraction) beads. The bead was maintained at the trap center by AOD feedback every 4 nm (blue arrows in A). (A) A trace with detected steps (in red) for single kinesin moving at a velocity similar to dynein (5 nm/sec). (B, F, H and J) Simulated tracks with detected steps for kinesin (39 steps), dynein with 8nm steps only, dynein (number of steps = 659) and CCB-dynein (48 steps). (C, D, G, I and K) Step size distributions determined from experiment (blue star, real tracks such as in Fig. 3A and B) and simulated tracks with real noise (red circles) for single-molecule kinesin with plus end directed 8 nm steps only, kinesin involving back-steps, dynein with minus end directed 8 nm steps only and for single dynein with and without CCB (45 steps used in K). Purple open circles are the residual, indicating difference between distributions. (E) Integrated residual from (C) and (D) is smaller when back-steps are for kinesin are included. (L) Normalized step probability for dynein with and without CCB. (M) Steps were detected from video tracking traces (48 traces) of moving beads coated with dynein or dynein/ CCB (3 frames/sec) without force feedback. Step distributions are in qualitative agreement with step detection from AODs. 4 WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
Supplementary Figure 5 A Y-Position (nm) 5 7 35-35 -7 Kinesin Experiment (mm ATP) B 7 35-35 -7 Y-Position (nm) 5 Kinesin Experiment (mm ATP) Detected Steps C Count 5 Kinesin ( mm ATP) Standard Deviation 3. nm -8 - -6 6 8 Y- Bead Position (nm) F Y-Position (nm)...4.6.8.. X-position (m) D Count 5 5 Kinesin (AMP-PNP) Standard Deviation 3..77 nm 75 Dynein 4 5 7 35-35 -7-5..5..5. -8 - -6 6 8 Y- Bead Position (nm) G Y-Position (nm)..5..5. E 75 CCB-Dynein 4 5 7 35-35 -7-5 3 4 5 Time (Sec) Dynein (No ATP) Dynein CCB-Dynein.4. Counts(Normalized).6. 4 6 8 Steps (nm) Supplementary Figure 5 Characterization of lateral motion. Beads with adsorbed kinesin, dynein, or dynein plus the p5 Glued CCB fragment were analyzed for bead motion perpendicular to the microtubule long axis (Y- bead position). (A) Example traces of Y-bead position vs. time for kinesin at saturating ATP. (B) Detected steps (red lines) from (A). (C) Gaussian distribution of detected steps (5 processive bead). (D) Lateral step size distribution of kinesin in the presence of AMP-PNP ( beads checked). Distributions in (C) and (D) are similar indicating that kinesin does not take lateral steps. (E) Lateral step size distributions of dynein without ATP (black) or dynein (blue), and dynein with CCB (red) with saturating ATP (48 lateral steps). (F and G) are example traces of Y-FLOP of bead for dynein and CCB-dynein. WWW.NATURE.COM/NATURECELLBIOLOGY 5 4 Macmillan Publishers Limited. All rights reserved.
Supplementary Figure 6 A Supernatant Pellet 5 kda Dynein HC 5 kda p5-555 p35-cc CC 5 kda CCB CCA Full scan for Fig D Supplementary Figure 6 Full scans of immunoblots and gels from Fig. and Fig. 6. A) Full scan for Fig. D. B) Full scan for Fig. E panel. (C) Full scan for Fig. E, panels -4. (D) Full scan for FigE, panel 5. (E) Full scan for Fig. 6A. (F) Full scan for Fig 6B, upper panel. (G) Full scan for Fig. 6B, middle panel. (H) Full scan for Fig. 6B, lower panel. 6 WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
B S P S P 5 kda MTs CCB kda Full scan for Fig E panel Supplementary Figure 6 continued WWW.NATURE.COM/NATURECELLBIOLOGY 7 4 Macmillan Publishers Limited. All rights reserved.
C S P S P S P S P S P S P p5-555 5 kda p35-cc CC/MTs kda Full scan for Fig E panels -4 Supplementary Figure 6 continued 8 WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
D.4uM 4uM S P S P S P S P S P S P S P S P S P S P 5 kda MTs kda CCA Full scan for Fig E panel 5 Supplementary Figure 6 continued WWW.NATURE.COM/NATURECELLBIOLOGY 9 4 Macmillan Publishers Limited. All rights reserved.
E Input Supernatant Pellet GST-CCA 5 kda CCB GST 5 kda Full scan for Fig 6A Supplementary Figure 6 continued WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
F Input M 6 8 4 6 8 4 6 8 3 5 kda CCB 5 kda Full scan for Fig 6B upper panel Supplementary Figure 6 continued WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
G Input M 6 8 4 6 8 4 6 8 3 5 kda 5 kda CCA Full scan for Fig 6B middle panel Supplementary Figure 6 continued WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
H Input M 6 8 4 6 8 4 6 8 3 5 kda 5 kda CCB CCA Full scan for Fig 6B lower panel Supplementary Figure 6 continued WWW.NATURE.COM/NATURECELLBIOLOGY 3 4 Macmillan Publishers Limited. All rights reserved.
4 C Alpha Helices Beta Strands Turns/ Unordered Θ/Θ8 CC.984.6.6 CCB.98.9.5 CCA.983.7.9 p35 CC.944..34.7-555.355.48.497.96 5 C Alpha Helices Beta Strands Turns/ Unordered Θ/Θ8 predicted coiled- coil content CC.975.5..75.94 CCB.975.5..5.95 CCA.974..3.6.865 p35 CC.94.4.35.8.758-555.36.5.487.97.58 37 C Alpha Helices Beta Strands Turns/ Unordered Θ/Θ8 CC.665.3.34.964 CCB.359.5.59.65 CCA.579.6.394.84 p35 CC.944..34.956-555.38.6.5.89 Supplementary Table Summary of circular dichroism (CD) data for p5 Glued fragments. The fraction a-helix, b-sheet, or disordered structure for each fragment was calculated from molar ellipticities measured at 4, 5 and 37 C. A ratio of molar ellipticities q / q 8 > indicates coiled-coil a-helical structure. Predicted coiled-coil a-helical content was determined with COILS. CD data for the shorter fragments corresponded well with predicted coiled-coil content. p35-cc showed more a-helical content than is predicted to form from the coiled-coil region, suggesting N-terminal regions are a-helical. In contrast, p5 Glued -555 showed less a-helical content, indicating that the coiled-coil region may be unfolded in this fragment. 4 WWW.NATURE.COM/NATURECELLBIOLOGY 4 Macmillan Publishers Limited. All rights reserved.
Step Size (nm) - 3-4 - 6 - - 8 8 6 4 Kinesin 5.5 94.5 Dynein.5 7.5 8.5 38.5 3 6.5.5 CCB- Dynein 5 9.5 8.5 3.5.5 6 3 Supplementary Table Stepping behavior summary for kinesin, dynein, and dynein + CCB. Frequency of steps as a function of size. Step size was determined as described in Methods. (3 independent experiments were used to verify the reproducibility). WWW.NATURE.COM/NATURECELLBIOLOGY 5 4 Macmillan Publishers Limited. All rights reserved.