posted on 2020-07-30, 21:30authored byJie Zheng, Timothy S. Strutzenberg, Adrian Reich, Venkatasubramanian Dharmarajan, Bruce D. Pascal, Gogce C. Crynen, Scott J. Novick, Ruben D. Garcia-Ordonez, Patrick R. Griffin
Hydrogen/Deuterium
Exchange (HDX) coupled with Mass Spectrometry
(HDX-MS) is a sensitive and robust method to probe protein conformational
changes and protein–ligand interactions. HDX-MS relies on successful
proteolytic digestion of target proteins under acidic conditions to
localize perturbations in exchange behavior to protein structure.
The ability of the protease to produce small peptides and overlapping
fragments and provide sufficient coverage of the protein sequence
is essential for localizing regions of interest. While the acid protease
pepsin has been the enzyme of choice for HDX-MS studies, recently,
it was shown that aspartic proteases from carnivorous pitcher plants
of the genus Nepenthes are active under low-pH conditions
and cleave at basic residues that are “forbidden” in
peptic digests. In this report, we describe the utility of one of
these enzymes, Nepenthesin II (NepII), in a HDX-MS workflow. A systematic
and statistical analysis of data from 11 proteins (6391 amino acid
residues) digested with immobilized porcine pepsin or NepII under
conditions compatible with HDX-MS was performed to examine protease
cleavage specificities. The cleavage of pepsin was most influenced
by the amino acid residue at position P1. Phe, Leu, and Met are favored
residues, each with a cleavage probability of greater than 40%. His,
Lys, Arg, or Pro residues prohibit cleavage when found at the P1 position.
In contrast, NepII offers advantageous cleavage to all basic residues
and produces shortened peptides that could improve the spatial resolution
in HDX-MS studies.