Construction and evaluation of novel fusion proteins for targeted delivery of micro particles to cellulose surfaces
Article first published online: 3 MAY 2006
Copyright © 2006 Wiley Periodicals, Inc.
Biotechnology and Bioengineering
Volume 94, Issue 4, pages 625–632, 5 July 2006
How to Cite
Lewis, W., Keshavarz-Moore, E., Windust, J., Bushell, D. and Parry, N. (2006), Construction and evaluation of novel fusion proteins for targeted delivery of micro particles to cellulose surfaces. Biotechnol. Bioeng., 94: 625–632. doi: 10.1002/bit.20849
- Issue published online: 29 MAY 2006
- Article first published online: 3 MAY 2006
- Manuscript Accepted: 19 DEC 2005
- Manuscript Received: 8 JUN 2005
- fusion protein;
The use of IgG antibodies and fragments has been limited to specific sectors of the biotechnology industry due to the high cost of producing large batches of product necessary for alternative applications. A novel class of Camelid antibodies, known as VHH offer a more economical opportunity to meet a wider application in industry. In this study, we report the evaluation of four llama VHH-cellulose binding domain fusion proteins displaying varying formats of VHH and CBD domains. Proteins were characterized in a targeted particle delivery system as a method of delivering agents such as perfume to laundry in the wash cycle. Fusion proteins were shown to be stable at high pH and in the presence of a detergent base. They were also shown to bind effectively to both the designated antigen, the azo-dye reactive-red 6 (either conjugated to BSA or attached to coacervate microparticles), and cellulose. Binding strength differences were observed between the different fusion protein formats using surface plasmon resonance. The effect of key laundry ingredients was also studied. Combining the fusion proteins and particles into a delivery and deposition study generated clear microscopy evidence for bifunctionality. Confirmation of this was validated by GC-MS analysis of retained fragrance. This research, reporting the construction and characterization of a variety of fusion proteins, illustrates that the single multidomain fusion protein route offers a new technology for successful targeted delivery of encapsulated benefit agents. Furthermore, the potential to modify or select for proteins to recognize a wide range of surfaces is also possible. © 2006 Wiley Periodicals, Inc.