I am working on PLA-PEG nanoparticles and wondering if I can do NHS/EDC chemistry to conjugate CGKRK to acid terminated end of PLA-PEG. Majority of the reports are on using the thiol group in Cysteine to work out a thiol-maleimide click reaction. I am wondering if that is due to the fact that NHS/EDC might perturb the free amine residues of the lysine thereby rendering the peptide unfunctional.