A systems approach to model natural variation in reactive properties of bacterial ribosomes
A systems approach to model natural variation in reactive properties of bacterial ribosomes
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DOI:
10.1186/1752-0509-2-62
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发表时间:
2008-07-13
影响因子:
--
通讯作者:
Herring, Patricia A.
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文献类型:
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作者:
Jackson, Julius H.;Schmidt, Thomas M.;Herring, Patricia A.
Background: Natural variation in protein output from translation in bacteria and archaea may be an organism-specific property of the ribosome. This paper adopts a systems approach to model the protein output as a measure of specific ribosome reactive properties in a ribosome-mediated translation apparatus. We use the steady-state assumption to define a transition state complex for the ribosome, coupled with mRNA, tRNA, amino acids and reaction factors, as a subsystem that allows a focus on the completed translational output as a measure of specific properties of the ribosome.Results: In analogy to the steady-state reaction of an enzyme complex, we propose a steady-state translation complex for mRNA from any gene, and derive a maximum specific translation activity, T-a(max), as a property of the ribosomal reaction complex. T-a(max) has units of a-protein output per time per a-specific mRNA. A related property of the ribosome, (T) over tilde (a(max)), has units of a-protein per time per total RNA with the relationship (T) over tilde (a(max)) = rho a T-a(max), where rho(a) represents the fraction of total RNA committed to translation output of P-a from gene a message. T-a(max) as a ribosome property is analogous to k(cat) for a purified enzyme, and (T) over tilde (a(max)) is analogous to enzyme specific activity in a crude extract.Conclusion: Analogy to an enzyme reaction complex led us to a ribosome reaction model for measuring specific translation activity of a bacterial ribosome. We propose to use this model to design experimental tests of our hypothesis that specific translation activity is a ribosomal property that is subject to natural variation and natural selection much like V-max and K-m for any specific enzyme.