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Updated: Apr 29, 2026

Analyzing Large Protein Complexes by Structural Mass Spectrometry
Published on: June 19, 2010
The use of targeted proteomics to determine the stoichiometry of large macromolecular assemblies
Alessandro Ori1, Amparo Andrés-Pons1, Martin Beck1
1European Molecular Biology Laboratory, Structural and Computational Biology Unit, Meyerhofstr. 1, 69117, Heidelberg, Germany.
Abstract:
Accurate knowledge of the stoichiometry of protein complexes is a crucial prerequisite for understanding their structure and function. To purify or enrich large and intricate protein complexes such that their structure is preserved and to absolutely quantify all of their protein components is an enormous technical challenge. In this chapter, we describe how to purify nuclear envelopes from human tissue culture cells that are highly enriched for nuclear pore complexes. We use the nuclear pore as an example to discuss how the structural preservation of such preparations can be controlled. Furthermore, we give a practical guide how to develop and employ targeted proteomic assays for both, the absolute quantification of stoichiometries and the relative quantification of protein complex composition across multiple biological conditions. The concept discussed here is universally applicable to any protein complex.
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