A Caltech Library Service

Structure of a β-Alanine-linked Polyamide Bound to a Full Helical Turn of Purine Tract DNA in the 1:1 Motif

Urbach, Adam R. and Love, John J. and Ross, Scott A. and Dervan, Peter B. (2002) Structure of a β-Alanine-linked Polyamide Bound to a Full Helical Turn of Purine Tract DNA in the 1:1 Motif. Journal of Molecular Biology, 320 (1). pp. 55-71. ISSN 0022-2836. doi:10.1016/S0022-2836(02)00430-8.

Full text is not posted in this repository. Consult Related URLs below.

Use this Persistent URL to link to this item:


Polyamides composed of N-methylpyrrole (Py), N-methylimidazole (Im) and N-methylhydroxypyrrole (Hp) amino acids linked by β-alanine (β) bind the minor groove of DNA in 1:1 and 2:1 ligand to DNA stoichiometries. Although the energetics and structure of the 2:1 complex has been explored extensively, there is remarkably less understood about 1:1 recognition beyond the initial studies on netropsin and distamycin. We present here the 1:1 solution structure of ImPy–β–Im–β–ImPy–β-Dp bound in a single orientation to its match site within the DNA duplex 5′-CCAAAGAGAAGCG-3′·5′-CGCTTCTCTTTGG-3′ (match site in bold), as determined by 2D 1H NMR methods. The representative ensemble of 12 conformers has no distance constraint violations greater than 0.13 Å and a pairwise RMSD over the binding site of 0.80 Å. Intermolecular NOEs place the polyamide deep inside the minor groove, and oriented N–C with the 3′–5′ direction of the purine-rich strand. Analysis of the high-resolution structure reveals the ligand bound 1:1 completely within the minor groove for a full turn of the DNA helix. The DNA is B-form (average rise=3.3 Å, twist=38°) with a narrow minor groove closing down to 3.0–4.5 Å in the binding site. The ligand and DNA are aligned in register, with each polyamide NH group forming bifurcated hydrogen bonds of similar length to purine N3 and pyrimidine O2 atoms on the floor of the minor groove. Each imidazole group is hydrogen bonded via its N3 atom to its proximal guanine's exocyclic amino group. The important roles of β-alanine and imidazole for 1:1 binding are discussed.

Item Type:Article
Related URLs:
URLURL TypeDescription
Dervan, Peter B.0000-0001-8852-7306
Additional Information:© 2002 Elsevier Science Ltd. Received 7 February 2002; received in revised form 26 April 2002; accepted 29 April 2002. The authors thank Professor Tammy Dwyer for generously providing the ligand force–field parameters. Professor Dwyer and Professor David Case provided many helpful suggestions that led to significant improvements in the structure calculations. We are grateful to Jason Schnell for assembling the ligand in LEaP and for helpful discussions. A.R.U. thanks Professor Tom James for help with MARDIGRAS and Professor Richard Lavery for help with CURVES. This work was supported by the National Institutes of Health (GM 27681).
Funding AgencyGrant Number
Subject Keywords:NMR structure; β-alanine; polyamides; purine tract; DNA recognition
Issue or Number:1
Record Number:CaltechAUTHORS:20160510-081406162
Persistent URL:
Official Citation:Adam R. Urbach, John J. Love, Scott A. Ross, Peter B. Dervan, Structure of a β-Alanine-linked Polyamide Bound to a Full Helical Turn of Purine Tract DNA in the 1:1 Motif, Journal of Molecular Biology, Volume 320, Issue 1, 28 June 2002, Pages 55-71, ISSN 0022-2836, (
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:66816
Deposited By: Victoria Brennan
Deposited On:18 May 2016 18:54
Last Modified:11 Nov 2021 00:03

Repository Staff Only: item control page