a. Will keeping the FMOC on it work? Can I do that and couple through some distal Lys amino groups with N-hydroxysuccinimide activated macromolecule, and then deprotect the peptide?
b. Is there some other protection strategy that is good for this?
c.) Of course I can insert a Cys and couple through -SH, but I'd rather not if I don't need to.
d.) And I could get elaborate and engineer a site for proteolytic cleavage which would leave my desired N-terminus, but surely this won't be necessary?
I'd appreciate any thoughts.
Tom Andersen
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Thomas T. Andersen, Ph.D.
Protein Chemistry Core Facility
Albany Medical College
Albany, NY 12208
518 262-5368
518 262-5689 fax
anderst@mail.amc.edu