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. 2011 Mar 21;11(3):3327–3355. doi: 10.3390/s110303327

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© 2011 by the authors; licensee MDPI, Basel, Switzerland.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).

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Figure 5. — Two-dimensional diblock copolymer templates of PS-b-PVP and protein assembly behavior observed on them; (a) various nanoscale templates resulting from chemical modification of nanodomains in micellar-forming diblock copolymers, (b and c) immunoglobulin G molecules on (b) open and (c) reverted PS-b-PVP templates, and (d) mushroom tyrosinase molecules assembled on a reverted PS-b-PVP template. The atomic force microscopy (AFM) scan size in panels (b) through (d) corresponds to (b): (2) 300 × 300 nm, (3) 180 × 180 nm, and (c and d): (2) 300 × 300 nm, (3) 180 × 180 nm. Adapted with permission from [100].

Figure 5. — Two-dimensional diblock copolymer templates of PS-b-PVP and protein assembly behavior observed on them; (a) various nanoscale templates resulting from chemical modification of nanodomains in micellar-forming diblock copolymers, (b and c) immunoglobulin G molecules on (b) open and (c) reverted PS-b-PVP templates, and (d) mushroom tyrosinase molecules assembled on a reverted PS-b-PVP template. The atomic force microscopy (AFM) scan size in panels (b) through (d) corresponds to (b): (2) 300 × 300 nm, (3) 180 × 180 nm, and (c and d): (2) 300 × 300 nm, (3) 180 × 180 nm. Adapted with permission from [100].