Cross-linking mass spectrometry (XL-MS) has become an
indispensable
tool for the emerging field of systems structural biology over the
recent years. However, the confidence in individual protein–protein
interactions (PPIs) depends on the correct assessment of individual
inter-protein cross-links. In this article, we describe a mono- and
intralink filter (mi-filter) that is applicable to any kind of cross-linking
data and workflow. It stipulates that only proteins for which at least
one monolink or intra-protein cross-link has been identified within
a given data set are considered for an inter-protein cross-link and
therefore participate in a PPI. We show that this simple and intuitive
filter has a dramatic effect on different types of cross-linking data
ranging from individual protein complexes over medium-complexity affinity
enrichments to proteome-wide cell lysates and significantly reduces
the number of false-positive identifications for inter-protein links
in all these types of XL-MS data