Nonspecifically bound proteins spin while diffusing along DNA

被引:263
作者
Blainey, Paul C. [2 ]
Luo, Guobin [2 ]
Kou, S. C. [5 ]
Mangel, Walter F. [3 ]
Verdine, Gregory L. [2 ,4 ]
Bagchi, Biman [1 ]
Xie, X. Sunney [2 ]
机构
[1] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
[2] Harvard Univ, Dept Chem & Biol Chem, Cambridge, MA 02138 USA
[3] Brookhaven Natl Lab, Dept Biol, Upton, NY 11973 USA
[4] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[5] Harvard Univ, Dept Stat, Ctr Sci, Cambridge, MA 02138 USA
关键词
FACILITATED TARGET LOCATION; STRUCTURAL BASIS; RNA-POLYMERASE; REPAIR; TRANSCRIPTION; RECOGNITION; KINETICS; MOTION; CELL;
D O I
10.1038/nsmb.1716
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is known that DNA-binding proteins can slide along the DNA helix while searching for specific binding sites, but their path of motion remains obscure. Do these proteins undergo simple one-dimensional (1D) translational diffusion, or do they rotate to maintain a specific orientation with respect to the DNA helix? We measured 1D diffusion constants as a function of protein size while maintaining the DNA-protein interface. Using bootstrap analysis of single-molecule diffusion data, we compared the results to theoretical predictions for pure translational motion and rotation-coupled sliding along the DNA. The data indicate that DNA-binding proteins undergo rotation-coupled sliding along the DNA helix and can be described by a model of diffusion along the DNA helix on a rugged free-energy landscape. A similar analysis including the 1D diffusion constants of eight proteins of varying size shows that rotation-coupled sliding is a general phenomenon. The average free-energy barrier for sliding along the DNA was 1.1 +/- 0.2 k(B)T. Such small barriers facilitate rapid search for binding sites.
引用
收藏
页码:1224 / U34
页数:7
相关论文
共 25 条
[1]   Diffusion constant of a nonspecifically bound protein undergoing curvilinear motion along DNA [J].
Bagchi, Biman ;
Blainey, Paul C. ;
Xie, X. Sunney .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (19) :6282-6284
[2]   Structure of a DNA glycosylase searching for lesions [J].
Banerjee, A ;
Santos, WL ;
Verdine, GL .
SCIENCE, 2006, 311 (5764) :1153-1157
[3]   Structure of a repair enzyme interrogating undamaged DNA elucidates recognition of damaged DNA [J].
Banerjee, A ;
Yang, W ;
Karplus, M ;
Verdine, GL .
NATURE, 2005, 434 (7033) :612-618
[4]   DIFFUSION-DRIVEN MECHANISMS OF PROTEIN TRANSLOCATION ON NUCLEIC-ACIDS .1. MODELS AND THEORY [J].
BERG, OG ;
WINTER, RB ;
VONHIPPEL, PH .
BIOCHEMISTRY, 1981, 20 (24) :6929-6948
[5]   A base-excision DNA-repair protein finds intrahelical lesion bases by fast sliding in contact with DNA [J].
Blainey, PC ;
van Oijent, AM ;
Banerjee, A ;
Verdine, GL ;
Xie, XS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (15) :5752-5757
[6]   Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA [J].
Bruner, SD ;
Norman, DPG ;
Verdine, GL .
NATURE, 2000, 403 (6772) :859-866
[7]  
Efron B., 1993, MONOGR STAT APPL PRO, V57
[8]   Probing transcription factor dynamics at the single-molecule level in a living cell [J].
Elf, Johan ;
Li, Gene-Wei ;
Xie, X. Sunney .
SCIENCE, 2007, 316 (5828) :1191-1194
[9]   Structural basis of transcription:: An RNA polymerase II elongation complex at 3.3 Å resolution [J].
Gnatt, AL ;
Cramer, P ;
Fu, JH ;
Bushnell, DA ;
Kornberg, RD .
SCIENCE, 2001, 292 (5523) :1876-1882
[10]   Protein motion from non-specific to specific DNA by three-dimensional routes aided by supercoiling [J].
Gowers, DM ;
Halford, SE .
EMBO JOURNAL, 2003, 22 (06) :1410-1418