The mustard trypsin inhibitor MTI-2 is a potential tool in the study of int
eractions between pest insects and plants. It can be applied to study the a
daptations of digestive proteases in pest insects. Phage display allows a r
apid and exhaustive system for the selection of heterologous protein varian
ts with novel specificities. Here we describe a bacteriophage expression sy
stem which permits functional expression of MTI-2 variants. Active and inac
tive mutants of NITI-S are constructed and displayed on phage. These are us
ed to demonstrate that an active variant can be selected from a background
of 10,000 inactive mutants in four rounds of selection and amplification. (
C) 2001 Academic Press.