4.8 Article

Structure of a DNA glycosylase searching for lesions

Journal

SCIENCE
Volume 311, Issue 5764, Pages 1153-1157

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1120288

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Funding

  1. NCI NIH HHS [R01 CA100742] Funding Source: Medline
  2. NIGMS NIH HHS [F32 GM067380, R01 GM044853, GM044853] Funding Source: Medline

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DNA glycosylases must interrogate millions of base pairs of undamaged DNA in order to locate and then excise one damaged nucleobase. The nature of this search process remains poorly understood. Here we report the use of disulfide cross-linking (DXL) technology to obtain structures of a bacterial. DNA glycosylase, MutM, interrogating undamaged DNA. These structures, solved to 2.0 angstrom resolution, reveal the nature of the search process: The protein inserts a probe residue into the helical stack and severely buckles the target base pair, which remains intrahelical. MutM therefore actively interrogates the intact DNA helix white searching for damage.

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