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Dissecting the Dynamic Pathways of Stereoselective DNA Threading Intercalation

Almaqwashi, A. A. (författare)
Northeastern University,Northeastern Univ, Dept Phys, Boston, MA 02115 USA.
Andersson, Johanna, 1983 (författare)
Uppsala universitet,Institutionen för kemi - BMC,Chalmers, Dept Chem & Chem Engn, S-41296 Gothenburg, Sweden.,Chalmers tekniska högskola,Chalmers University of Technology
Lincoln, Per, 1958 (författare)
Chalmers tekniska högskola,Chalmers University of Technology,Chalmers, Dept Chem & Chem Engn, S-41296 Gothenburg, Sweden.
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Rouzina, I. (författare)
Ohio State University,Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA.
Westerlund, Fredrik, 1978 (författare)
Chalmers tekniska högskola,Chalmers University of Technology,Chalmers, Dept Biol & Biol Engn, S-41296 Gothenburg, Sweden.
Williams, M. C. (författare)
Northeastern University,Northeastern Univ, Dept Phys, Boston, MA 02115 USA.
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Northeastern University Northeastern Univ, Dept Phys, Boston, MA 02115 USA (creator_code:org_t)
Elsevier BV, 2016
2016
Engelska.
Ingår i: Biophysical Journal. - : Elsevier BV. - 0006-3495 .- 1542-0086. ; 110:6, s. 1255-1263
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • DNA intercalators that have high affinity and slow kinetics are developed for potential DNA-targeted therapeutics. Although many natural intercalators contain multiple chiral subunits, only intercalators with a single chiral unit have been quantitatively probed. Dumbbell-shaped DNA threading intercalators represent the next order of structural complexity relative to simple intercalators, and can provide significant insights into the stereoselectivity of DNA-ligand intercalation. We investigated DNA threading intercalation by binuclear ruthenium complex [mu-dppzip(phen)(4)Ru-2](4+) (Piz). Four Piz stereoisomers are defined by the chirality of the intercalating subunit (Ru(phen)(2)dppz) and the distal subunit (Ru(phen)(2)ip), respectively, each of which can be either right-handed (Delta) or left-handed (Lambda). We used optical tweezers to measure single DNA molecule elongation due to threading intercalation, revealing force-dependent DNA intercalation rates and equilibrium dissociation constants. The force spectroscopy analysis provided the zero-force DNA binding affinity, the equilibrium DNA-ligand elongation Delta x(eq), and the dynamic DNA structural deformations during ligand association x(on) and dissociation x(off). We found that Piz stereoisomers exhibit over 20-fold differences in DNA binding affinity, from a K-d of 27 +/- 3 nM for (Delta,Lambda)-Piz to a K-d of 622 +/- 55 nM for (Lambda,Delta)-Piz. The striking affinity decrease is correlated with increasing Delta x(eq) from 0.30 +/- 0.02 to 0.48 +/- 0.02 nm and x(on) from 0.25 +/- 0.01 to 0.46 +/- 0.02 nm, but limited x(off) changes. Notably, the affinity and threading kinetics is 10-fold enhanced for right-handed intercalating subunits, and 2- to 5-fold enhanced for left-handed distal subunits. These findings demonstrate sterically dispersed transition pathways and robust DNA structural recognition of chiral intercalators, which are critical for optimizing DNA binding affinity and kinetics.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biofysik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biophysics (hsv//eng)

Nyckelord

single dna
actinomycin-d
binuclear ruthenium complex
molecule
optical tweezers
binding-kinetics
noncooperative binding
equilibrium
affinity
force spectroscopy
Biophysics

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