Literature DB >> 8107097

Co-operative binding of Escherichia coli SSB tetramers to single-stranded DNA in the (SSB)35 binding mode.

M E Ferrari1, W Bujalowski, T M Lohman.   

Abstract

Escherichia coli SSB tetramers can bind to single stranded (ss) DNA in several binding modes. At 25 degrees C, pH 8.1, SSB can form at least three distinct binding modes, (SSB)n, where the number of nucleotides occluded per tetramer (n), can have values of 35, 56 or 65. Stability of the different modes is modulated by solution conditions, primarily the salt concentration and type, as well as the free SSB concentration. At least two different types of positive co-operative binding of SSB to ssDNA have also been observed, which appear to be correlated with different SSB binding modes. The (SSB)65 mode, which dominates at monovalent salt concentrations > 0.2 M, displays only moderate, "limited" co-operative binding in which clustering of SSB is limited to the formation of dimers of tetramers (octamers). However, at lower salt concentrations, "unlimited" co-operative binding is observed in which long SSB clusters can form, similar to the behavior observed for the phage T4 gene 32 protein. It has been proposed that unlimited co-operativity is linked to the (SSB)35 binding mode; however, this has not been verified since quantitative estimates of the co-operativity in this binding mode are difficult on long ssDNA. To estimate the nearest-neighbor co-operativity parameter in the (SSB)35 mode, we have examined the equilibrium binding of SSB to the oligodeoxynucleotide, dA(pA)69. Under certain conditions, 1:1 complexes, in which all four SSB subunits interact with the dA(pA)69, can form at low SSB binding densities, whereas 2:1 complexes, in which both SSB tetramers bind to DNA using only two subunits, can form at high SSB binding densities. These 2:1 complexes serve as a model for co-operative binding in the (SSB)35 binding mode. We show that SSB tetramers bind in this mode with a minimum nearest-neighbor co-operativity parameter of omega 35 = 1.0 x 10(5) (0.125 M NaCl, pH 8.1, 25 degrees C). This indicates that the nearest-neighbor co-operativities for SSB tetramers bound to ssDNA in the (SSB)35 versus the (SSB)65 mode differ qualitatively and quantitatively and suggests that the (SSB)35 mode is responsible for the ability of SSB protein to form long clusters on ssDNA. If the ability of helix destabilizing proteins to form uninterrupted protein clusters on ssDNA is important in DNA replication, then it is likely that SSB uses its (SSB)35 mode to function in this capacity.

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Year:  1994        PMID: 8107097     DOI: 10.1006/jmbi.1994.1122

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  49 in total

1.  Functional analysis of the four DNA binding domains of replication protein A. The role of RPA2 in ssDNA binding.

Authors:  S A Bastin-Shanower; S J Brill
Journal:  J Biol Chem       Date:  2001-07-30       Impact factor: 5.157

2.  Analytic binding isotherms describing competitive interactions of a protein ligand with specific and nonspecific sites on the same DNA oligomer.

Authors:  O V Tsodikov; J A Holbrook; I A Shkel; M T Record
Journal:  Biophys J       Date:  2001-10       Impact factor: 4.033

3.  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

4.  Nonspecific DNA binding and bending by HUαβ: interfaces of the three binding modes characterized by salt-dependent thermodynamics.

Authors:  Junseock Koh; Irina Shkel; Ruth M Saecker; M Thomas Record
Journal:  J Mol Biol       Date:  2011-04-12       Impact factor: 5.469

5.  Multiple C-terminal tails within a single E. coli SSB homotetramer coordinate DNA replication and repair.

Authors:  Edwin Antony; Elizabeth Weiland; Quan Yuan; Carol M Manhart; Binh Nguyen; Alexander G Kozlov; Charles S McHenry; Timothy M Lohman
Journal:  J Mol Biol       Date:  2013-09-07       Impact factor: 5.469

6.  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

7.  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

8.  Protein Environment and DNA Orientation Affect Protein-Induced Cy3 Fluorescence Enhancement.

Authors:  Binh Nguyen; Monika A Ciuba; Alexander G Kozlov; Marcia Levitus; Timothy M Lohman
Journal:  Biophys J       Date:  2019-06-07       Impact factor: 4.033

9.  The human mitochondrial single-stranded DNA-binding protein displays distinct kinetics and thermodynamics of DNA binding and exchange.

Authors:  Yufeng Qian; Kenneth A Johnson
Journal:  J Biol Chem       Date:  2017-06-14       Impact factor: 5.157

10.  Structural Mechanisms of Cooperative DNA Binding by Bacterial Single-Stranded DNA-Binding Proteins.

Authors:  Katarzyna Dubiel; Angela R Myers; Alexander G Kozlov; Olivia Yang; Jichuan Zhang; Taekjip Ha; Timothy M Lohman; James L Keck
Journal:  J Mol Biol       Date:  2018-11-22       Impact factor: 5.469

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