Three-dimensional structural analysis of eukaryotic flagella/cilia by electron cryo-tomography

Based on the molecular architecture revealed by electron cryo-tomography, the mechanism of the bending motion of eukaryotic flagella/cilia is discussed.


Introduction
Flagella and cilia are bending organelles in eukaryotic cells and are responsible for cellular motility or the flow of extracellular fluid (Fig. 1a). The axoneme, the bending core of flagella and cilia, has a '9 + 2' structure, where nine microtubule doublets surround two singlet microtubules. Adjacent microtubule doublets are connected by dynein heavy chains (ATP-driven motor proteins) and other linkers to form a sliding motion (Fig. 1b). Dynein motor proteins form two complexes, the inner and outer dynein arms, responsible for waveform determination and force generation, respectively. Inner dynein arms contain eight dynein heavy chains and form the 96 nm periodicity along microtubule doublets, whereas outer dynein arms have two or three heavy chains with 24 nm periodicity (Fig. 1c). Each dynein heavy chain (total 4500 amino acids) has an N-terminal tail (1500 amino acids), six AAA rings and a coiled-coil stalk (between the fourth and the fifth AAA domains) (Fig. 1d). The N-terminal tail is anchored on one microtubule (A-MT), while the coiled-coil stalk dynamically interacts with the adjacent microtubule (B-MT) in an ATP-dependent manner.
Although the basic architecture of this '9 + 2' axoneme is shared among most of the species, the waveform of the flagella shows amazing diversity depending on the species, organelles and conditions. For example, sperm flagella generate a symmetric waveform, while the waveform of Tetrahymena cilia is asymmetric. Normally Chlamydomonas cells swim toward the light with two flagella making a breast-stroke-like asymmetric waveform, whereas they swim backward with a sperm-like symmetric waveform under intense light. This conversion is regulated by calcium concentration. There should be a mechanism to integrate the sliding and bending of microtubule doublets driven by dynein into such a highly orchestrated flagellar/ciliary motion with well defined waveforms.
Despite previous two-dimensional image analysis of dynein heavy chains in vitro (Burgess et al., 2003;Ueno et al., 2008), the mechanisms of the power stroke of dynein and flagellar/ ciliary bending motion were not known. To address this, threedimensional structural analysis of dynein arms in flagella/cilia is required. NMR (Benashski et al., 1999) and X-ray crystallography (Carter et al., 2009) successfully solved the structure of a light chain and of a microtubule-binding domain of the dynein heavy chain (Fig. 1e), respectively. Nevertheless, the full-length dynein heavy chain is still a very challenging target for such methods, and mainly analyzed by single-particle analysis from electron micrographs (Samso & Koonce, 2004). However, single-particle analysis, which requires the assumption that particles in micrographs are projections of an identical three-dimensional structure seen from random orientations, is not suitable for visualization of molecules in such a heterogeneous environment as flagella, where density from dyneins is overlapped with other molecules and dynein itself has heterogeneity owing to flexible domains. For this purpose, electron tomography is a potential approach to obtain the three-dimensional molecular structure in situ despite the limitation of resolution owing to radiation damage and the missing wedge described in the following two sections. In this research we acquired electron micrographs of iceembedded flagella (thickness $ 0.3 mm), enabling us to observe the intact structure without artefacts from staining, fixation and flattening on carbon grids, tilted from À60 to +60 with a 2 increment angle using a CCD camera at a very low ($ 0.5 e À Å À2 ) electron dose (Ishikawa et al., 2007). Acquired images were aligned using colloidal gold particles (Fig. 2a).
Here we describe our recent in situ structural analysis of dynein and other proteins in flagella using electron cryotomography and propose a mechanism for flagellar/ciliary motion and its regulation of the waveform.

Electron dose and radiation damage for electron cryo-tomography
Frozen hydrated biological specimens (embedded in amorphous ice) have low contrast (Fig. 2b) and high sensitivity to the electron beam. This is particularly important in the case of tomography, since the specimen must be illuminated multiple times and radiation damage is more severe than in other methods. To improve the signal-to-noise ratio, we utilized the periodicity of flagella (24 nm and 96 nm for outer and inner dynein arms, respectively) by averaging these periodic units, first along each microtubule doublet (Fig. 2c) and then among nine doublets (Fig. 2d). However, to extract fragments with periodicity and align them for averaging, contrast is required. More illumination gives higher contrast, but radiation damage suppresses the resolution. We must therefore find the optimized conditions to obtain sufficient contrast and sufficient resolution to address our requirements.
We acquired datasets at relatively low dose conditions ($ 30 e À Å À2 in total) to reveal the three-dimensional conformation of dynein heavy chains (described in x4), and relatively high dose conditions ($ 60 e À Å À2 ) when we map the arrangement of proteins in flagella to determine asymmetry (see x5). The three-dimensional reconstruction from images acquired under low-dose conditions shows less contrast (Fig. 2c), but, after averaging, presents higher resolution than individual images under the high-dose condition (Fig. 2d).

Missing wedge
Another problem with electron tomography is the missing wedge. Owing to technical problems (highly tilted samples are very thick owing to the projection at those angles and do not allow the electron beam to fully penetrate), the specimen can be tilted to only a limited angle (in our case 60 ). Since one transmission electron micrograph, which is a projection of the object in real space, corresponds to a section in threedimensional Fourier space, practical tomographic datasets can cover only a limited area and information is missing for wedge-shaped areas in threedimensional Fourier space. This causes an artificial distortion of the threedimensional reconstruction (Lucic et al., 2005).
Indeed, in the vertical section of our tomogram of a flagellum, contrast of the microtubule doublets is weak in the direction perpendicular to the electron beam (i.e. horizontal), whereas the edges parallel to the beam (i.e. vertical) are not distorted (Fig. 2a). The flagellar membrane is over-amplified in the vertical direction (arrows in Fig. 2b) and vanishes in the horizontal direction. However, the problem is avoided by averaging nine microtubule doublets which are oriented differently and thus have different orientations of the missing wedge. After averaging, the cross section of a microtubule doublet shows an isotropic density distribution with each protofilament clearly visible (Fig. 2d).

Conformation of outer and inner dynein arms in flagella
Based on the above approach, we reconstructed in situ threedimensional structures of periodic units containing a microtubule doublet, outer and inner dynein arms as well as other proteins in flagella from green algae Chlamydomonas reinhardtii (Fig. 3a) (Ishikawa et al., 2007;Bui et al., 2008). Three outer arm dynein heavy chains stack on the A-MT vertically, whereas eight inner arm dyneins form a collinear array. Comparison of mutants lacking some isoforms of inner and outer arm dyneins with the wild-type enabled us to identify the locations of those isoforms and also the positions of AAA rings and N-terminal tails (Fig. 3b). All the dyneins have Nterminal tails extending from the AAA ring toward the distal end (i.e. tip of the flagellum and plus-end of the microtubule), except the outer arm heavy chain whose conformation is not yet clear. This suggests that all the dyneins generate force in the same direction. However, orientations of AAA rings show variety. Some dyneins may generate torque to control waveforms.
Kinetics studies (Holzbaur & Johnson, 1989) proved that the power stroke of dynein occurs during product (ADP and/ or phosphate) release. Therefore, to understand the structural basis of the power stroke, we compared the three-dimensional structure of the outer and inner dynein arms with and without nucleotides (Movassagh et al., 2010). We trapped the dynein ATPase cycle at the ADP.Pi state by adding vanadate. Compared with the structure in the presence of ADP and vanadate, the positions of the AAA rings are shifted toward the distal end in the absence of nucleotides (apo) (Figs. 3c and 3d). The orientation of the coiled-coil stalk is invariant during the power stroke. This result indicates that the AAA ring shifts (but does not rotate) to pull the adjacent B-MT during product release (Fig. 3e).

Asymmetry of the dynein arrangement on nine microtubule doublets
It is still unclear how the sliding and bending motions of each pair of adjacent microtubule doublets are integrated into a well defined waveform. Electron cryo-tomography of Chlamydomonas flagella supplied us with an insight (Bui et al., 2009) (Fig. 4). Under the conditions of relatively high electron dose, the differences between the architecture of dyneins among nine microtubule doublets were detected. Seven of nine doublets share an identical dynein arrangement. However, one doublet (doublet 9) lacks one inner arm dynein (dynein b/g) (Figs. 4c and 4d). Furthermore, we realised an abnormality in the adjacent doublet (doublet 1). It lacks a few inner arm dyneins or they are mis-folded or replaced by other molecules (Figs. 4e and 4f).  Asymmetry was detected in other proteins linking microtubule doublets (Fig. 4g). Although nexin links all the adjacent pairs of microtubule doublets, we found two more linker proteins connecting only limited pairs of doublets: IDL2 exists between 4 and 5, 5 and 6, and 9 and 1, whereas IDL3 links doublets 1 and 2. These linkers are plotted almost in the plane of bending. They probably suppress the sliding motion between microtubule doublets, restricting the motion in the plane. Localized defects of the inner arm dyneins could make this planar bending asymmetric.

Discussion
Our results demonstrate the potential of electron cryo-tomography as a method for visualizing molecular arrangement, conformation and dynamics in situ. Current optics and detectors techniques limit the resolution of electron cryotomography to $ 35 Å . Even in this resolution range we could analyze the location and the conformation of dynein by utilizing mutants. Tagging techniques such as immunogold labeling and GFP fusion will be helpful as well. For image analysis at atomic resolution, we must combine the in situ structure from tomography with the high-resolution structure from crystallography, NMR or single-particle analysis.