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Dynamics and Mechanism of DNA-Bending Proteins in Binding Site Recognition - Yogambigai Velmurugu

Dynamics and Mechanism of DNA-Bending Proteins in Binding Site Recognition

Buch | Softcover
XXI, 199 Seiten
2018 | 1. Softcover reprint of the original 1st ed. 2017
Springer International Publishing (Verlag)
978-3-319-83218-0 (ISBN)
CHF 164,75 inkl. MwSt
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Using a novel approach that combines high temporal resolution of the laser T-jump technique with unique sets of fluorescent probes, this study unveils previously unresolved DNA dynamics during search and recognition by an architectural DNA bending protein and two DNA damage recognition proteins.

Many cellular processes involve special proteins that bind to specific DNA sites with high affinity.  How these proteins recognize their sites while rapidly searching amidst ~3 billion nonspecific sites in genomic DNA remains an outstanding puzzle. Structural studies show that proteins severely deform DNA at specific sites and indicate that DNA deformability is a key factor in site-specific recognition. However, the dynamics of DNA deformations have been difficult to capture, thus obscuring our understanding of recognition mechanisms. 

The experiments presented in this thesis uncover, for the first time, rapid (~100-500 microseconds) DNA unwinding/bending attributed to nonspecific interrogation, prior to slower (~5-50 milliseconds) DNA kinking/bending/nucleotide-flipping during recognition. These results help illuminate how a searching protein interrogates DNA deformability and eventually "stumbles" upon its target site. Submillisecond interrogation may promote preferential stalling of the rapidly scanning protein at cognate sites, thus enabling site-recognition.  Such multi-step search-interrogation-recognition processes through dynamic conformational changes may well be common to the recognition mechanisms for diverse DNA-binding proteins. 

Yogambigai Velmurugu was awarded the PhD degree by the University of Illinois, Chicago, in 2015.

Introduction.- Methods.- Integration Host Factor (IHF)-DNA interaction.- Lesion Recognition by Xeroderma Pigmentosum C (XPC) Protein.- DNA Mismatch Repair.

Erscheinungsdatum
Reihe/Serie Springer Theses
Zusatzinfo XXI, 199 p. 112 illus., 105 illus. in color.
Verlagsort Cham
Sprache englisch
Maße 155 x 235 mm
Gewicht 349 g
Themenwelt Naturwissenschaften Biologie Biochemie
Naturwissenschaften Chemie Analytische Chemie
Naturwissenschaften Physik / Astronomie Angewandte Physik
Schlagworte Dynamics of protein DNA interactions • Equlibrium FRET measurements • Integration Host Factor (IHF)-DNA interaction • Laser temperature-jump spectroscopy • Protein-induced DNA bending • Protein-Ligand Interactions
ISBN-10 3-319-83218-2 / 3319832182
ISBN-13 978-3-319-83218-0 / 9783319832180
Zustand Neuware
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