Localization and orientation of the γ-Tubulin Small Complex components using protein tags as labels for single particle EM |
| |
Authors: | Rebeca M Choy Justin M Kollman Alex Zelter Trisha N Davis David A Agard |
| |
Institution: | aDepartment of Biochemistry and Biophysics and the Howard Hughes Medical Institute, University of California, San Francisco, CA 94158, United States;bDepartment of Biochemistry, University of Washington, Seattle, WA 98195, United States |
| |
Abstract: | γ-Tubulin Small Complex (γ-TuSC) is the universally-conserved complex in eukaryotes that contains the microtubule (MT) nucleating protein: γ-tubulin. γ-TuSC is a heterotetramer with two copies of γ-tubulin and one copy each of Spc98p and Spc97p. Previously, the structure of γ-TuSC was determined by single particle electron microscopy (EM) at 25 Å resolution. γ-TuSC is Y-shaped with a single flexible arm that could be the key to regulating MT nucleation. EM gold labeling revealed the locations of γ-tubulin at the top of the Y. In vivo Fluorescence Resonance Energy Transfer (FRET) suggested the relative orientations of Spc98p and Spc97p but did not distinguish which large subunit formed the flexible arm. Here, using fluorescent proteins as covalently attached tags, we used class averages and 3-D random conical tilt reconstructions to confirm the in vivo FRET results, clearly demonstrating that the Spc98p/97p C-termini interact directly with γ-tubulin. Most significantly we have determined that the flexible arm belongs to Spc98p and our data also suggests that the N-termini of Spc98p and Spc97p are crossed. More generally, our results confirm that despite their small size, covalently-attached fluorescent proteins perform well as subunit labels in single particle EM. |
| |
Keywords: | γ -TuSC Tub4p γ -Tubulin Spc98p Spc97p Electron microscopy labeling |
本文献已被 ScienceDirect 等数据库收录! |
|