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PMID: 12590603 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Validation Study

Evaluation of a modular strategy for the construction of novel polydactyl zinc finger DNA-binding proteins.

Biochemistry ·Vol. 42 ·No. 7 ·2003-02-25 ·Pages 2137-48

Segal DJ, Beerli RR, Blancafort P, Dreier B, Effertz K, Huber A, Koksch B, Lund CV, Magnenat L, Valente D, Barbas CF

Abstract

In previous studies, we have developed a technology for the rapid construction of novel DNA-binding proteins with the potential to recognize any unique site in a given genome. This technology relies on the modular assembly of modified zinc finger DNA-binding domains, each of which recognizes a three bp subsite of DNA. A complete set of 64 domains would provide comprehensive recognition of any desired DNA sequence, and new proteins could be assembled by any laboratory in a matter of hours. However, a critical parameter for this approach is the extent to which each domain functions as an independent, modular unit, without influence or dependence on its neighboring domains. We therefore examined the detailed binding behavior of several modularly assembled polydactyl zinc finger proteins. We first demonstrated that 80 modularly assembled 3-finger proteins can recognize their DNA target with very high specificity using a multitarget ELISA-based specificity assay. A more detailed analysis of DNA binding specificity for eight 3-finger proteins and two 6-finger proteins was performed using a target site selection assay. Results showed that the specificity of these proteins was as good or better than that of zinc finger proteins constructed using methods that allow for interdependency. In some cases, near perfect specificity was achieved. Complications due to target site overlap were found to be restricted to only one particular amino acid interaction (involving an aspartate in position 2 of the alpha-helix) that occurs in a minority of cases. As this is the first report of target site selection for designed, well characterized 6-finger proteins, unique insights are discussed concerning the relationship of protein length and specificity. These results have important implications for the design of proteins that can recognize extended DNA sequences, as well as provide insights into the general rules of recognition for naturally occurring zinc finger proteins.

MeSH Terms
DNA/chemical synthesis DNA-Binding Proteins/chemical synthesis Enzyme-Linked Immunosorbent Assay/methods Oligonucleotides/chemical synthesis Protein Binding Protein Engineering/methods Protein Structure, Tertiary Recombinant Fusion Proteins/chemical synthesis Repetitive Sequences, Amino Acid Transcription Factors/chemical synthesis Zinc Fingers
Chemicals
DNA-Binding Proteins Oligonucleotides Recombinant Fusion Proteins Transcription Factors DNA
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Segal David J
The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, California 92037, USA. [email protected]
Beerli Roger R
Blancafort Pilar
Dreier Birgit
Effertz Karin
Huber Adrian
Koksch Beate
Lund Caren V
Magnenat Laurent
Valente David
Barbas Carlos F
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
2003-02-25
Pages
2137-48
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIAID NIH HHS · AI41944 · United States
NCI NIH HHS · CA86258 · United States
NIDDK NIH HHS · DK61803 · United States
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