Chemical cross-linking combined with mass spectrometry
(CXMS) has
emerged as a powerful tool to study protein structure, conformation,
and protein–protein interactions (PPIs). Until now, most cross-linked
peptides were generated by using commercial cross-linkers, such as
DSS, BS3, and DSSO, which react with the primary amino
groups of the lysine residues of proteins. However, trypsin, the most
commonly used proteolytic enzyme, cannot cleave the C-terminus of
a linked lysine, making the obtained cross-linked peptides longer
than common peptides and unfavorable for MS identification and data
searching. Herein, we propose an in situ sequential digestion strategy
using enzymes with distinct cleavage specificity, named as smart cutter,
to generate cross-linked peptides with suitable length so that the
identification coverage could improve. Through the application of
such a strategy to DSS cross-linked E. coli lysates,
additional cross-linked sites (1.3-fold increase) obtained in comparison
with those obtained by trypsin–trypsin digestion (2879 vs 1255).
Among the different digestion combinations, AspN-trypsin performed
the best, with 64% (673/1059) of the cross-linked sites complementary
to trypsin–trypsin digestion, which is beneficial to ensure
the depth for studying protein structure and PPIs. Taking the 60 kDa
chaperonin protein as an example, more than twice the cross-linked
sites (30 vs 14) were identified to enrich the protein structure information.
In addition, compared to the published protein interaction network
for E. coli (http://www.bacteriome.org), 91 potential PPIs were discovered
with our strategy, of which 65 have not covered by trypsin–trypsin
digestion. Therefore, these results illustrate the great significance
of smart-cutter-based CXMS for the revelation of protein structure
as well as finding new PPIs.