Literature DB >> 8193130

Effects of base composition on the negative cooperativity and binding mode transitions of Escherichia coli SSB-single-stranded DNA complexes.

T M Lohman1, W Bujalowski.   

Abstract

We have examined the ability of the Escherichia coli single-stranded DNA binding protein (SSB) tetramer to form its different binding modes on poly(dC), poly(U), and poly(A) over a range of NaCl and NaF concentrations for comparison with previous studies with poly(dT). In reverse titrations with poly(U) and poly(A) at 25 degrees C, pH 8.1, SSB forms all four binding modes previously observed with poly(dT), namely, (SSB)35, (SSB)40, (SSB)56, and (SSB)65, where the subscript denotes the site size (i.e., the average number of nucleotides occluded per SSB tetramer). As with poly(dT), the low site size modes are favored at low monovalent salt concentration (< 10 mM), whereas increasing salt concentration facilitates the transitions to the higher site size modes. Surprisingly, SSB does not form a stable (SSB)35 complex on poly(dC), even at 1 mM NaCl; rather, the (SSB)56 mode is formed under these conditions. Upon raising the [NaCl], the (SSB)56 complex undergoes a transition to the (SSB)65 complex (transition midpoint, 40 mM NaCl). On the basis of studies with dC(pC)34, dT(pT)34, and dA(pA)34, the inability of the SSB tetramer to form the (SSB)35 complex with poly(dC) is due mainly to a much lower degree of negative cooperativity for binding oligodeoxycytidylates to the SSB tetramer. At low salt concentration, the negative cooperativity parameter, sigma 35, is lowest for dA(pA)34, intermediate for dT(pT)34, and highest for dC(pC)34, indicating that it is most difficult to saturate the SSB tetramer with two molecules of dA(pA)34. We have also measured the equilibrium constants for binding the oligodeoxynucleotides dC(pC)34, dC(pC)69, dA(pA)34, and dA(pA)69 as a function of [NaCl] and [NaBr] and find that the salt dependencies of these oligonucleotides are dependent upon base composition. These studies also indicate that ion binding accompanies formation of these SSB-ss-DNA complexes, although there is a net release of ions upon formation of the complex. This influence of both salt concentration and base composition indicates that both electrostatic and nonelectrostatic factors contribute to the negative cooperativity associated with ss-DNA binding to the SSB tetramer.

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Year:  1994        PMID: 8193130     DOI: 10.1021/bi00186a016

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  12 in total

1.  E. coli SSB tetramer binds the first and second molecules of (dT)(35) with heat capacities of opposite sign.

Authors:  Alexander G Kozlov; Timothy M Lohman
Journal:  Biophys Chem       Date:  2011-05-12       Impact factor: 2.352

2.  Effects of monovalent anions on a temperature-dependent heat capacity change for Escherichia coli SSB tetramer binding to single-stranded DNA.

Authors:  Alexander G Kozlov; Timothy M Lohman
Journal:  Biochemistry       Date:  2006-04-25       Impact factor: 3.162

3.  Saccharomyces cerevisiae replication protein A binds to single-stranded DNA in multiple salt-dependent modes.

Authors:  Sangaralingam Kumaran; Alexander G Kozlov; Timothy M Lohman
Journal:  Biochemistry       Date:  2006-10-03       Impact factor: 3.162

4.  Intrinsically disordered C-terminal tails of E. coli single-stranded DNA binding protein regulate cooperative binding to single-stranded DNA.

Authors:  Alexander G Kozlov; Elizabeth Weiland; Anuradha Mittal; Vince Waldman; Edwin Antony; Nicole Fazio; Rohit V Pappu; Timothy M Lohman
Journal:  J Mol Biol       Date:  2015-01-03       Impact factor: 5.469

5.  Ultrafast redistribution of E. coli SSB along long single-stranded DNA via intersegment transfer.

Authors:  Kyung Suk Lee; Amanda B Marciel; Alexander G Kozlov; Charles M Schroeder; Timothy M Lohman; Taekjip Ha
Journal:  J Mol Biol       Date:  2014-05-02       Impact factor: 5.469

6.  Regulation of single-stranded DNA binding by the C termini of Escherichia coli single-stranded DNA-binding (SSB) protein.

Authors:  Alexander G Kozlov; Michael M Cox; Timothy M Lohman
Journal:  J Biol Chem       Date:  2010-04-01       Impact factor: 5.157

7.  The impact of base stacking on the conformations and electrostatics of single-stranded DNA.

Authors:  Alex Plumridge; Steve P Meisburger; Kurt Andresen; Lois Pollack
Journal:  Nucleic Acids Res       Date:  2017-04-20       Impact factor: 16.971

Review 8.  SSB-DNA binding monitored by fluorescence intensity and anisotropy.

Authors:  Alexander G Kozlov; Roberto Galletto; Timothy M Lohman
Journal:  Methods Mol Biol       Date:  2012

Review 9.  The tale of SSB.

Authors:  Piero R Bianco
Journal:  Prog Biophys Mol Biol       Date:  2016-11-09       Impact factor: 3.667

10.  Escherichia coli single-stranded DNA-binding protein mediates template recycling during transcription by bacteriophage N4 virion RNA polymerase.

Authors:  Elena K Davydova; Lucia B Rothman-Denes
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-22       Impact factor: 11.205

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