| Literature DB >> 25661992 |
Jonathan Walklate1, Michael A Geeves2.
Abstract
Conducting enzymatic stopped-flow experiments at temperatures far removed from ambient can be very problematic because extremes in temperature (<10°C or >30°C) can damage the machine or the enzyme. We have devised a simple manifold that can be attached to most commercial stopped-flow systems that is independently heated or cooled separate from the main stopped-flow system. Careful calibration of the flow circuit allows the sample to be heated or cooled to the measurement temperature (-8 to +40°C) 1 to 2s before mixing in the reaction chamber. This approach allows measurements at temperatures where the stopped flow or the protein is normally unstable. To validate the manifold, we investigated the well-defined ATP-induced dissociation of rabbit muscle myosin subfragment 1 (S1) from its complex with pyrene-labeled actin. This process has both temperature-dependent and -independent components. Use of ethylene glycol allowed us to measure the reaction below 0°C and up to 42°C, and as expected the second-order rate constant (K1k+2) and the maximum rate of dissociation (k+2) both increased with temperature, whereas 1/K1 is unaffected by the change in temperature.Entities:
Keywords: Fast reactions; Physiological temperatures; Subzero temperatures; Transient kinetics
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Year: 2015 PMID: 25661992 DOI: 10.1016/j.ab.2015.01.020
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365