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Chudinov, I. K.

Publications and source records attributed to Chudinov, I. K..

2 recordsLinked to original sources

Affordable 96-parallel SPPS: hardware and software add-on for automated liquid handling platforms

ParSynt-P is a hardware and software add-on that converts a liquid-handling robot already available in a proteomics laboratory (Tecan Freedom EVO) into a parallel plate-format peptide synthesizer for generating libraries of candidate peptide standards for targeted blood plasma proteomics. The manifold is milled from polytetrafluoroethylene and has ports for an inert gas and a vacuum line; a standard commercially available 96-well filtration plate is secured to it with an airtight seal. The software layer generates robot worklists from a table of peptide sequences and controls switching of the N?/vacuum lines, including pulsed gas mixing. The system performs up to 96 syntheses per run, and coupling of one residue takes 94 min. Workability of this 96-well format was verified on three fully loaded plates. The uniformity of synthesis conversion across the plate was measured quantitatively using a characterized NAT/SIL standard pair. The add-on cost $351, while the synthesis cost is $0.23 per coupling and $1.14 per milligram of crude product, an order of magnitude below the market price of custom synthesis.

biochemistry↗

Direct empirical in-house assessment of peptide proteotypicity for targeted proteomics

In bottom-up proteomics peptide it was early shown that despite a certain protein is present in a sample, only a subset of its proteolytic peptide products will be detected with LC-MS analysis. Property of peptide being frequently detected given its source proteins identification was called proteotypicity. Much effort has been since applied to predict proteotypic peptides and summarize evidence on peptide detection. Nevertheless, when targeted proteomics method is being developed, prediction or inference from communal experience might be inaccurate and prior knowledge of true peptide proteotypicity in a selected setup for a selected population is necessary. In this work we test fully in-house approach for proteotypicity assessment including comprehensive peptide synthesis and detection verification. Proteotypicity and contribution of sample processing and biology-related factors are estimated in a model experiment for three plasma proteins, albumin, ceruloplasmin and C-reactive protein.

genomics↗