bioRxivBiochemistryPreprint
Synthetic biology meets proteomics: Construction of a la carte QconCATs for absolute protein quantification
J. R. Johnson, V. M. Harman, C. de Matos Ferraz Franco, N. R. Rockliffe, Y. Sun, L. Liu, A. Takemori, N. Takemori, R. J. Beynon
Abstract
We report a new approach to the assembly and construction of QconCATs, quantitative concatamers for proteomic applications that yield stoichiometric quantities of sets of stable isotope-labelled internal standards. The new approach is based on synthetic biology precepts of biobricks, making use of loop assembly to construct larger entities from individual biobricks. It offers a major gain in flexibility of QconCAT implementation and enables rapid and efficient editability that permits, for example, substitution of one peptide for another. The basic building block (a Qbrick) is a segment of DNA that encodes two or more quantification peptides for a single protein, readily held in a repository as a library resource. These Qbricks are then assembled in a one tube ligation reaction that enforces the order of assembly, to yield short QconCATs that are useable for small quantification products. However, the DNA context of the short also allows a second cycle of assembly such that five different short QconCATs can be assembled into a longer QconCAT in a second, single tube ligation. From a library of Qbricks, a bespoke QconCAT can be assembled quickly and efficiently in a form suitable for expression and labelling in vivo or in vitro. We refer to this approach as the ALACAT strategy as it permits a la carte design of quantification standards.
- assay: proteomics
- research focus: protein folding & dynamics
- research focus: software / tool
- research focus: benchmarking
- approach: experimental assay
- approach: wet-lab / biochemical assay
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