Ultrafast water dynamics at the interface of the polymerase-DNA binding complex.

ABSTRACT: DNA polymerases slide on DNA during replication, and the interface must be mobile for various conformational changes. The role of lubricant interfacial water is not understood. In this report, we systematically characterize the water dynamics at the interface and in the active site of a tight binding polymerase (pol β) in its binary complex and ternary state using tryptophan as a local optical probe. Using femtosecond spectroscopy, we observed that upon DNA recognition the surface hydration water is significantly confined and becomes bound water at the interface, but the dynamics are still ultrafast and occur on the picosecond time scale. These interfacial water molecules are not trapped but are mobile in the heterogeneous binding nanospace. Combining our findings with our previous observa

SUBMITTER: Yang Y 

PROVIDER: S-EPMC4148141 | biostudies-literature | 2014 Aug

REPOSITORIES: biostudies-literature