In this review, we summarize design strategies for generating proteins with
desired sequences such as long contiguous base pairs and diverse sequence
specificities based on the nature of Cys(2)-His(2) zinc finger proteins. Re
cent progress towards artificial DNA binding proteins has been achieved by
structure-based design processes and by selection strategies. Indeed, a mul
ti-zinc finger protein with an 18 (or 27)-base pair address, and new zinc f
inger proteins for diverse DNA target sites (TATA-box and p53 binding site)
have been created successfully. Such novel zinc finger proteins will proba
bly be useful tools in molecular biology and potentially in human medicine.
(C) 2001 Elsevier Science B.V. All rights reserved.