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Cited by 401

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Genetically encoded short peptide tag for versatile protein labeling by Sfp phosphopantetheinyl transferase

Open access
Yin, Jun, Straight, Paul D., McLoughlin, Shaun M., Zhou, Zhe, Lin, Alison J., Golan, David E., Kelleher, Neil L., Kolter, Roberto, Walsh, Christopher T.·2005·Proceedings of the National Academy of Sciences

Abstract

An 11-residue peptide with the sequence D S LEFIASKLA was identified from a genomic library of Bacillus subtilis by phage display as an efficient substrate for Sfp phosphopantetheinyl transferase-catalyzed protein labeling by small molecule-CoA conjugates. We name this peptide the “ybbR tag,” because part of its sequence is derived from the ybbR ORF in the B. subtilis genome. The site of Sfp-catalyzed ybbR tag labeling was mapped to the underlined Ser residue, and the ybbR tag was found to have a strong tendency for adopting an α-helical conformation in solution. Here we demonstrate that the ybbR tag can be fused to the N or C termini of target proteins or inserted in a flexible loop in the middle of a target protein for site-specific protein labeling by Sfp. The short size of the ybbR tag and its compatibility with various target proteins, the broad substrate specificity of Sfp for labeling the ybbR tag with small-molecule probes of diverse structures, and the high specificity and efficiency of the labeling reaction make Sfp-catalyzed ybbR tag labeling an attractive tool for expanding protein structural and functional diversities by posttranslational modification.

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Crossref · 10.1073/pnas.0507705102

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Metadata

Authors
Yin, J., Straight, P. D., McLoughlin, S. M., Zhou, Z., Lin, A. J., Golan, D. E., Kelleher, N. L., Kolter, R., & Walsh, C. T.
Venue
Proceedings of the National Academy of Sciences
Published
2005-10-19
Volume
102
Issue
44
Pages
15815-15820
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2150881786
Cited by
401
References
2
FWCI
3.92
Type
journal article
Language
en
Open access
green

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