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DNA Cross-Linking with Metallointercalator−Peptide Conjugates

Copeland, Kimberly D. and Lueras, Alexis M. K. and Stemp, Eric D. A. and Barton, Jacqueline K. (2002) DNA Cross-Linking with Metallointercalator−Peptide Conjugates. Biochemistry, 41 (42). pp. 12785-12797. ISSN 0006-2960. doi:10.1021/bi020407b. https://resolver.caltech.edu/CaltechAUTHORS:20160210-155329163

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Abstract

Short peptides have been tethered to a DNA−intercalating ruthenium complex to create a photoactivated cross-linking reagent. The ruthenium complex, [Ru(phen)(bpy‘)(dppz)]^(2+) (phen = 1,10-phenanthroline, bpy‘ = 4-(butyric acid)-4‘-methyl-2,2‘-bipyridine, and dppz = dipyridophenazine), delivers the peptide to DNA and initiates the cross-linking reaction by oxidizing DNA upon irradiation in the presence of an oxidative quencher. The tethered peptide, only five to six residues in length, forms cross-links with the oxidized site in DNA. Cross-linking was detected and studied by gel electrophoresis and through spectroscopic measurements. The ruthenium−peptide complex is luminescent when bound to DNA, and the binding constants for several intercalator−peptide conjugates were determined by luminescence titration. The composition of the peptide affects both binding affinity and the extent of cross-linking. The greatest amounts of cross-linking were observed with tethered peptides that contained positively charged residues, either lysine or arginine. To test the impact of individual residues on cross-linking, the central residue in a 5-mer peptide was substituted with seven different amino acids. Though mutation of this position had only a small effect on the extent of cross-linking, it was discovered that peptides containing Trp or Tyr gave a distinctive pattern of products in gels. In experiments using the untethered peptide and ruthenium complex, it was determined that delivery of the peptide by the ruthenium intercalator is not essential for cross-linking; peptide attachment to the metal complex can constrain cross-linking. Importantly, the cross-linking adducts produced with ruthenium−peptide conjugates are luminescent and thus provide a luminescent cross-linking probe for DNA.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1021/bi020407bDOIArticle
http://pubs.acs.org/doi/abs/10.1021/bi020407bPublisherArticle
ORCID:
AuthorORCID
Stemp, Eric D. A.0000-0003-2098-4214
Barton, Jacqueline K.0000-0001-9883-1600
Additional Information:© 2002 American Chemical Society. Received June 7, 2002; Revised Manuscript Received August 21, 2002. Publication Date (Web): September 26, 2002. We are grateful to the Biopolymer Synthesis Facility at Caltech for the preparation of peptides, to Dr. Mona Shagoli for MALDI analysis of the cross-linking adducts, and to Dr. Hans-Achim Wagenknecht for synthesis of the ruthenium complex. This work was supported by the NIH (GM33309). The NIH also provided an NRSA predoctoral fellowship (K.D.C.), and the MURF program at Caltech provided a summer fellowship (A.M. K.L.).
Funders:
Funding AgencyGrant Number
NIHGM33309
NIH Predoctoral FellowshipUNSPECIFIED
Caltech Minority Undergraduate Research Fellowship (MURF)UNSPECIFIED
Issue or Number:42
DOI:10.1021/bi020407b
Record Number:CaltechAUTHORS:20160210-155329163
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20160210-155329163
Official Citation:DNA Cross-Linking with Metallointercalator−Peptide Conjugates Kimberly D. Copeland, Alexis M. K. Lueras, Eric D. A. Stemp, and Jacqueline K. Barton Biochemistry 2002 41 (42), 12785-12797 DOI: 10.1021/bi020407b
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:64392
Collection:CaltechAUTHORS
Deposited By: George Porter
Deposited On:11 Feb 2016 17:12
Last Modified:10 Nov 2021 23:30

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