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. Author manuscript; available in PMC: 2021 Jul 22.
Published in final edited form as: Adv Ther (Weinh). 2020 Feb 3;3(3):1900164. doi: 10.1002/adtp.201900164

Figure 3.

Figure 3.

Temperature-triggered self-assembly of an ELP block copolymers. a) An N-terminal hydrophilic ELP[V1A8G7-n] gene and C-terminal hydrophobic ELP[V5-n] gene are seamlessly fused together to create a gene that encodes an ELP block copolymer. When the size and ratio of the blocks are correctly selected, the ELP block copolymer self-assembles into a micelle close to body temperature. b) Hydrodynamic radius (Rh) and optical density profile at 350 nm of ELP[V1A8G7-64]/[[V5-90] block copolymer at 25 μm in PBS shows that ELPs exist as unimers (Rh of 5–10 nm) below CMT at 35 °C and form micelles (Rh 30–80 nm) above their CMT. c) Confocal fluorescence images of K562/αvβ3 cells treated with 10 μm ELP block copolymer with N terminal RGD ligand (green). Fluorescence images showed that there was no binding/uptake of RGD-ELP below the CMT but above the CMT there was significant binding/uptake of RGD-ELP due to the temperature-triggered multivalent display of RGD ligands. (a,b) Reproduced with permission.[50] Copyright 2007, American Chemical Society. (c) Reproduced with permission.[56] Copyright 2010, American Chemical Society.