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. Author manuscript; available in PMC: 2008 Oct 7.
Published in final edited form as: Biomacromolecules. 2007 Apr 4;8(5):1417–1424. doi: 10.1021/bm060849t

Figure 1.

Figure 1

Cloning scheme for cationic ELPs and their ELP fusion proteins showing coding DNA strand, the corresponding amino acid sequence, the ELP guest residue amino acids in bold, and the location of key endonuclease restrictions sites. PflM I and Bgl I restriction enzymes are used for recursive directional ligation to oligomerize ELP monomer genes in (A) as well as for gene excision for subcloning into pET expression vectors at the SfiI site shown in (B).