Directed evolution of the TALE N-terminal domain for recognition of all 5' bases.
Directed evolution of the TALE N-terminal domain for recognition of all 5' bases.
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DOI:
10.1093/nar/gkt754
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发表时间:
2013-11
影响因子:
14.9
通讯作者:
Barbas CF 3rd
中科院分区:
文献类型:
--
作者:
Lamb BM;Mercer AC;Barbas CF 3rd
Transcription activator-like effector (TALE) proteins can be designed to bind virtually any DNA sequence. General guidelines for design of TALE DNA-binding domains suggest that the 5′-most base of the DNA sequence bound by the TALE (the N0 base) should be a thymine. We quantified the N0 requirement by analysis of the activities of TALE transcription factors (TALE-TF), TALE recombinases (TALE-R) and TALE nucleases (TALENs) with each DNA base at this position. In the absence of a 5′ T, we observed decreases in TALE activity up to >1000-fold in TALE-TF activity, up to 100-fold in TALE-R activity and up to 10-fold reduction in TALEN activity compared with target sequences containing a 5′ T. To develop TALE architectures that recognize all possible N0 bases, we used structure-guided library design coupled with TALE-R activity selections to evolve novel TALE N-terminal domains to accommodate any N0 base. A G-selective domain and broadly reactive domains were isolated and characterized. The engineered TALE domains selected in the TALE-R format demonstrated modularity and were active in TALE-TF and TALEN architectures. Evolved N-terminal domains provide effective and unconstrained TALE-based targeting of any DNA sequence as TALE binding proteins and designer enzymes.
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影响因子:
14.9
作者:
Meckler JF;Bhakta MS;Kim MS;Ovadia R;Habrian CH;Zykovich A;Yu A;Lockwood SH;Morbitzer R;Elsäesser J;Lahaye T;Segal DJ;Baldwin EP
通讯作者:
Baldwin EP
影响因子:
46.9
作者:
通讯作者:
--
DOI:
10.1073/pnas.040552697
发表时间:
2000-02-15
影响因子:
11.1
作者:
Beerli, RR;Dreier, B;Barbas, CF
通讯作者:
Barbas, CF
影响因子:
56.9
作者:
Boch, Jens;Scholze, Heidi;Bonas, Ulla
通讯作者:
Bonas, Ulla
影响因子:
48
作者:
Gaj, Thomas;Guo, Jing;Kato, Yoshio;Sirk, Shannon J.;Barbas, Carlos F., III
通讯作者:
Barbas, Carlos F., III