The Structural Cell Biology (SCB) Core provides critical technologies and support for the Structural Cell? Biology of DNA Repair Machines (SBDR) Program. Major challenges of SBDR stem from the dynamic and? coordinated assembly of large protein complexes involved in DNA repair processes. These complexes? undergo functionally important conformational changes and modifications. The SCB Core will provide? structural expertise and technologies suitable for SBDR project and program Aims, create a functional bridge? between atomic resolution structures and molecular envelopes, and help close the gap between static crystal? structures and biologically relevant, multi-component macromolecular machines. In particular, the SCB Core? will provide SBDR with three distinct and complementary methods for structural analyses. (1) Multiwavelength? single crystal X-ray diffraction will provide high-resolution structures of discrete states. (2) Small? Angle X-ray Scattering (SAXS) will characterize the solution dynamics of protein complexes by visualizing? flexible regions and induced conformational changes. (3) Scanning Force Microscopy (SFM) of single? molecules, available through the Wyman lab, will provide information about DNA and protein dynamics, and? will reveal structural insight into heterogeneous mixtures previously inaccessible using crystallographic or? SAXS techniques. The SCB Core is designed to supply the SBDR projects with the necessary tools and? proficiency to overcome the structural biology challenges inherent to analysis of large complexes. The? requested funding provides staff to maximize interaction with the EMB Core and for SBDR use of the? Structurally Integrated Biology for Life Sciences (SIBYLS) beamline at the Advanced Light Source (ALS) at? the Lawrence Berkeley National Laboratories (LBNL). The SIBYLS beamline is a unique synchrotron? resource that provides tunable wavelengths for both single crystal X-ray diffraction and SAXS. The SCB? Core will develop software that addresses current limitations in the analysis of DNA repair proteins including? software that will combine results from high and low resolution techniques through the systematic and? objective fitting of X-ray crystal structures into molecular envelopes generated by EM and SAXS? experiments. The SCB Core will test, develop, and provide advanced tools to detect and measure posttranslational? modifications. Understanding the dynamic structures of macromolecular machines for DNA? repair will generate insights into multi-component systems that have remained elusive through the study of? individual component biomolecules. The results from the SCB Core will be applied to the understanding of? cancer etiology and potential cancer diagnostics and prognostics through interactions with the UCSF? Comprehensive Cancer Center.?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA092584-08
Application #
7683087
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2008-09-01
Budget End
2009-08-31
Support Year
8
Fiscal Year
2008
Total Cost
$2,222,882
Indirect Cost
Name
Lawrence Berkeley National Laboratory
Department
Type
DUNS #
078576738
City
Berkeley
State
CA
Country
United States
Zip Code
94720
Crickard, J Brooks; Kaniecki, Kyle; Kwon, Youngho et al. (2018) Meiosis-specific recombinase Dmc1 is a potent inhibitor of the Srs2 antirecombinase. Proc Natl Acad Sci U S A 115:E10041-E10048
Syed, Aleem; Tainer, John A (2018) The MRE11-RAD50-NBS1 Complex Conducts the Orchestration of Damage Signaling and Outcomes to Stress in DNA Replication and Repair. Annu Rev Biochem 87:263-294
Howes, Timothy R L; Sallmyr, Annahita; Brooks, Rhys et al. (2018) Erratum to ""Structure-activity relationships among DNA ligase inhibitors; characterization of a selective uncompetitive DNA ligase I inhibitor"" [DNA Repair 60C (2017) 29-39]. DNA Repair (Amst) 61:99
Bhattacharyya, Sudipta; Soniat, Michael M; Walker, David et al. (2018) Phage Mu Gam protein promotes NHEJ in concert with Escherichia coli ligase. Proc Natl Acad Sci U S A 115:E11614-E11622
Tsai, Chi-Lin; Tainer, John A (2018) Robust Production, Crystallization, Structure Determination, and Analysis of [Fe-S] Proteins: Uncovering Control of Electron Shuttling and Gating in the Respiratory Metabolism of Molybdopterin Guanine Dinucleotide Enzymes. Methods Enzymol 599:157-196
Ogorzalek, Tadeusz L; Hura, Greg L; Belsom, Adam et al. (2018) Small angle X-ray scattering and cross-linking for data assisted protein structure prediction in CASP 12 with prospects for improved accuracy. Proteins 86 Suppl 1:202-214
Langelier, Marie-France; Zandarashvili, Levani; Aguiar, Pedro M et al. (2018) NAD+ analog reveals PARP-1 substrate-blocking mechanism and allosteric communication from catalytic center to DNA-binding domains. Nat Commun 9:844
Crickard, J Brooks; Greene, Eric C (2018) Biochemical attributes of mitotic and meiotic presynaptic complexes. DNA Repair (Amst) :
Bhat, Kamakoti P; Krishnamoorthy, Archana; Dungrawala, Huzefa et al. (2018) RADX Modulates RAD51 Activity to Control Replication Fork Protection. Cell Rep 24:538-545
Sallmyr, Annahita; Tomkinson, Alan E (2018) Repair of DNA double-strand breaks by mammalian alternative end-joining pathways. J Biol Chem 293:10536-10546

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