Members of the cofilin/ADF family of proteins sever actin filaments, increasing the number of filament ends available for polymerization or depolymerization. Cofilin binds actin filaments with positive cooperativity, forming clusters of contiguously bound cofilin along the filament lattice. Filament severing occurs preferentially at boundaries between bare and cofilin-decorated (cofilactin) segments and is biased at 1 side of a cluster. A molecular understanding of cooperative binding and filament severing has been impeded by a lack of structural data describing boundaries. Here, we apply methods for analyzing filament cryo-electron microscopy (cryo-EM) data at the single subunit level to directly investigate the structure of boundaries within partially decorated cofilactin filaments. Subnanometer resolution maps of isolated, bound cofilin molecules and an actin-cofilactin boundary indicate that cofilin-induced actin conformational changes are local and limited to subunits directly contacting bound cofilin. An isolated, bound cofilin compromises longitudinal filament contacts of 1 protofilament, consistent with a single cofilin having filament-severing activity. An individual, bound phosphomimetic (S3D) cofilin with weak severing activity adopts a unique binding mode that does not perturb actin structure. Cofilin clusters disrupt both protofilaments, consistent with a higher severing activity at boundaries compared to single cofilin. Comparison of these structures indicates that this disruption is substantially greater at pointed end sides of cofilactin clusters than at the barbed end. These structures, with the distribution of bound cofilin clusters, suggest that maximum binding cooperativity is achieved when 2 cofilins occupy adjacent sites. These results reveal the structural origins of cooperative cofilin binding and actin filament severing.
机构:
Brandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USABrandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USA
Chin, Samantha M.
Jansen, Silvia
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Brandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USABrandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USA
Jansen, Silvia
Goode, Bruce L.
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Brandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USABrandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USA
机构:
Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USAYale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
De La Cruz, Enrique M.
Sept, David
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Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Computat Med & Bioinformat, Ann Arbor, MI 48109 USAYale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
机构:
Brandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USABrandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USA
Chin, Samantha M.
Jansen, Silvia
论文数: 0引用数: 0
h-index: 0
机构:
Brandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USABrandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USA
Jansen, Silvia
Goode, Bruce L.
论文数: 0引用数: 0
h-index: 0
机构:
Brandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USABrandeis Univ, Dept Biol, Rosenstiel Basic Med Sci Res Ctr, Waltham, MA 02454 USA
机构:
Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USAYale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
De La Cruz, Enrique M.
Sept, David
论文数: 0引用数: 0
h-index: 0
机构:
Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Computat Med & Bioinformat, Ann Arbor, MI 48109 USAYale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA