TY - JOUR
T1 - Structural comparison of purified dynein proteins with in situ dynein arms
AU - Goodenough, Ursula
AU - Heuser, John
N1 - Funding Information:
We thank Drs Kevin Pfister and George Witman (Worcester Foundation, Shrewsbury. JIA) for sending us an initial preparation of Chlamydomonas dynein, which convinced us t,hat this project was possible; Dr Kenneth Johnson (Pennsylvania State. University Park, PA) for providing us with his protocol for dynein purification prior to publication: Drs Tim ,Ilitchison and Marc Kirschner (U.C.S.F., San Francisco, CA) for purified tubulin; Dr Bessie Huang (Baylor College of Medicine, Houston. TX) for the $23 strain of Chlamydomonas: and Dr Steve Adair for his continued input and interest. A number of associates provided c.areful, indispensable help in this project: Carol Hwang cultured the cells; Brian Gebhart purified the dynein: Robyn Roth and Joe Hepfinger made the replicas; Lori Van Houten printed the final plat,es; Anne Dillon made the final drawings; and Jan Wuelling typed the manuscript. This work was supported by National Institutes of Healt’h grants GM-261 17 and GM-26150 to I’.W.G. and grant GM-29647 to J.E.H.
PY - 1984/12/25
Y1 - 1984/12/25
N2 - Using the quick-freeze deep-etch technique, we describe the structure of outer-arm dynein proteins from Chlamydomonas and Tetrahymena after adsorption to a mica surface, after high-salt dissociation, and after glutaraldehyde fixation, and compare these images to the configuration of outer arms bound to microtubules. After adsorption to mica, the extracted dyneins from both organisms look like three-headed "bouquets", as reported for Tetrahymena by Johnson & Wall (1983b). High magnification images demonstrate that each head carries a slender "stalk" and a long "stem", and that small subunits decorate the stems and create a "flowerpot" domain at the base of the bouquet. Exposure to high salt induces this trimer to dissociate into a two-headed species and a single-headed species; it also stimulates the decorative elements to dissociate from the stems. Dynein is thus constructed on the same general plan as myosin, with large globular heads, narrow stems and additional small subunits that associate with the stems. The splayed-out image of the bouquet appears to be a distortion arising during adsorption to mica since, after brief glutaraldehyde fixation, the three heads remain closely associated as vertices of a triangular unit. In situ, the three heads also adopt this trigonal configuration. Two of the three are visible from the exterior of the axoneme and constitute the bilobed rigor head we described previously (Goodenough & Heuser, 1982). The third head faces the interior of the axoneme where, we propose, it forms the "hook" of the outer arm as seen in thin section. We further propose that the decorative elements associated with the stem coalesce to form the two outer-arm "feet" seen in situ, and that at least one of the in vitro stalks is equivalent to the in situ stalk, which extends from the head to the B microtubule. Deep-etch images of stretched axonemes, partially extracted axonemes, and dynein-decorated brain microtubules indicate that each outer arm, as traditionally viewed, is a hybrid of two dynein molecules: its two feet derive from one molecule, whereas its trigonal head derives from the molecule located distally. The resultant overlapping configuration creates the diagonal "linkers" seen in situ, which correspond to the in vitro stems. Thus, a row of dynein arms is essentially a dynein polymer that extends from the tip to the base of a doublet microtubule, each head riding on its neighbor's feet like a row of circus elephants. Such dynein-dynein interactions may account for the co-operativity of dynein-microtubule binding, and may play an important role in generating ciliary motility.
AB - Using the quick-freeze deep-etch technique, we describe the structure of outer-arm dynein proteins from Chlamydomonas and Tetrahymena after adsorption to a mica surface, after high-salt dissociation, and after glutaraldehyde fixation, and compare these images to the configuration of outer arms bound to microtubules. After adsorption to mica, the extracted dyneins from both organisms look like three-headed "bouquets", as reported for Tetrahymena by Johnson & Wall (1983b). High magnification images demonstrate that each head carries a slender "stalk" and a long "stem", and that small subunits decorate the stems and create a "flowerpot" domain at the base of the bouquet. Exposure to high salt induces this trimer to dissociate into a two-headed species and a single-headed species; it also stimulates the decorative elements to dissociate from the stems. Dynein is thus constructed on the same general plan as myosin, with large globular heads, narrow stems and additional small subunits that associate with the stems. The splayed-out image of the bouquet appears to be a distortion arising during adsorption to mica since, after brief glutaraldehyde fixation, the three heads remain closely associated as vertices of a triangular unit. In situ, the three heads also adopt this trigonal configuration. Two of the three are visible from the exterior of the axoneme and constitute the bilobed rigor head we described previously (Goodenough & Heuser, 1982). The third head faces the interior of the axoneme where, we propose, it forms the "hook" of the outer arm as seen in thin section. We further propose that the decorative elements associated with the stem coalesce to form the two outer-arm "feet" seen in situ, and that at least one of the in vitro stalks is equivalent to the in situ stalk, which extends from the head to the B microtubule. Deep-etch images of stretched axonemes, partially extracted axonemes, and dynein-decorated brain microtubules indicate that each outer arm, as traditionally viewed, is a hybrid of two dynein molecules: its two feet derive from one molecule, whereas its trigonal head derives from the molecule located distally. The resultant overlapping configuration creates the diagonal "linkers" seen in situ, which correspond to the in vitro stems. Thus, a row of dynein arms is essentially a dynein polymer that extends from the tip to the base of a doublet microtubule, each head riding on its neighbor's feet like a row of circus elephants. Such dynein-dynein interactions may account for the co-operativity of dynein-microtubule binding, and may play an important role in generating ciliary motility.
UR - http://www.scopus.com/inward/record.url?scp=0021630304&partnerID=8YFLogxK
U2 - 10.1016/0022-2836(84)90272-9
DO - 10.1016/0022-2836(84)90272-9
M3 - Article
C2 - 6241263
AN - SCOPUS:0021630304
SN - 0022-2836
VL - 180
SP - 1083
EP - 1118
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 4
ER -