I am trying to quickly remember what happens to side chain amines (such as
beta of Dpr or epsilon of Lys) during edman degradation, for the sake of
determining what to expect on edman products by some MS experiments we are
going to perform.
Don't they also react with the PITC to form phenylthiocarbamyl derivatives
that don't cleave with TFA? Need your help.
Thanks,
Randy Wilhelm
Mallinckrodt, Inc
rrwilhe@mkg.com
(314)654-3965