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ReportsStructure of the Anaphase-Promoting Complex/Cyclosome Interacting with a Mitotic Checkpoint Complex![]() ![]()
Once all chromosomes are connected to the mitotic spindle (bioriented), anaphase is initiated by the protein ubiquitylation activity of the anaphase-promoting complex/cyclosome (APC/C) and its coactivator Cdc20 (APC/CCdc20). Before chromosome biorientation, anaphase is delayed by a mitotic checkpoint complex (MCC) that inhibits APC/CCdc20. We used single-particle electron microscopy to obtain three-dimensional models of human APC/C in various functional states: bound to MCC, to Cdc20, or to neither (apo-APC/C). These experiments revealed that MCC associates with the Cdc20 binding site on APC/C, locks the otherwise flexible APC/C in a "closed" state, and prevents binding and ubiquitylation of a wide range of different APC/C substrates. These observations clarify the structural basis for the inhibition of APC/C by spindle checkpoint proteins.
1 Research Institute of Molecular Pathology, Dr. Bohr-Gasse 7, 1030 Vienna, Austria.
2 Max-Planck-Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Goettingen, Germany. 3 European Molecular Biology Laboratory, Meyerhofstraße 1, 69117 Heidelberg, Germany. * Present address: Institute of Molecular Systems Biology, Eidgenössische Technische Hochschule Zurich, 8093 Zurich, Switzerland.
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Science. ISSN 0036-8075 (print), 1095-9203 (online)