Isolation of llama antibody fragments for prevention of dandruff by phage display in shampoo
Publication date
2005-01
Authors
Dolk, E.
Vaart, M. van der
Lutje Hulsik, D.
Vriend, G.
Haard, H. de
Spinelli, S.
Cambillau, C.
Frenken, L.
Verrips, T.
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Document Type
Article
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Abstract
As part of research exploring the feasibility of using antibody fragments to inhibit the growth of organisms
implicated in dandruff, we isolated antibody fragments that bind to a cell surface protein of Malassezia furfur
in the presence of shampoo. We found that phage display of llama single-domain antibody fragments (VHHs)
can be extended to very harsh conditions, such as the presence of shampoo containing nonionic and anionic
surfactants. We selected several VHHs that bind to the cell wall protein Malf1 of M. furfur, a fungus implicated
in causing dandruff. In addition to high stability in the presence of shampoo, these VHHs are also stable under
other denaturing conditions, such as high urea concentrations. Many of the stable VHHs were found to contain
arginine at position 44. Replacement of the native amino acid at position 44 with arginine in the most stable
VHH that lacked this arginine resulted in a dramatic further increase in the stability. The combination of the
unique properties of VHHs together with applied phage display and protein engineering is a powerful method
for obtaining highly stable VHHs that can be used in a wide range of applications.