首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Nano volume fractionation strategy for dilute-and-shoot injections in off-line loss-less proteomic workflows for extensive protein identifications of ultra-low sample amounts
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Nano volume fractionation strategy for dilute-and-shoot injections in off-line loss-less proteomic workflows for extensive protein identifications of ultra-low sample amounts

机译:纳米体积分馏策略,用于脱线损失蛋白质组学工作流量的稀释型蛋白质组学工作流程,用于超低样本量的广泛蛋白质鉴定

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摘要

A proteomic workflow for a simple loss-less manual nano-fractionation (300 nL/fraction) for low jig sample amounts which avoids the need to dry down or transfer fractions to autosampler vials is shown to be feasible. It is demonstrated that the conventional procedure of drying samples down followed by reconstitution negatively affects the number of protein and peptide identifications. Furthermore, these losses seem to disproportionately affect hydrophobic peptides from the drying down and reconstitution step. By collecting and concatenating the fractions while the outlet of the column is submerged in a small predefined volume of 0.2% formic acid, the content of acetonitrile in the collecting vials was lowered such that it was compatible with direct injection for the online analysis. This additionally resulted in a time gain of approx. an hour for the total fractionation time. Acetonitrile concentrations up to 7.5% do not seem to compromise the chromatographic performance in the online analysis. Using as little as 2 mu g digested HeLa lysate, approx. 7000 protein groups could be easily identified with 2 or more unique peptides. This was the case when fractionation was performed at pH 10 as well as at pH 5.5. (C) 2019 The Author(s). Published by Elsevier B.V.
机译:用于低夹具样品量的简单损失手动纳米分馏(300nl /级分)的蛋白质组学工作流程,其避免了对自动进样器小瓶的需要干燥或转移分数的需要是可行的。结果证明,将样品的常规程序进行下降,然后重构对蛋白质和肽鉴定的数量产生负面影响。此外,这些损失似乎不成比例地影响疏水性肽从干燥和重构步骤。通过在柱的出口被浸没在小预定体积的0.2%甲酸的小尺寸体积时收集和连接,降低了收集小瓶中乙腈的含量,使其与直接注射进行在线分析。这还导致时间增益约。总分级时间的一个小时。乙腈浓度高达7.5%似乎在在线分析中似乎不会损害色谱性能。使用少至2μg消化的Hela裂解物,约。可以用2个或更多个独特的肽容易地鉴定7000个蛋白质基团。这是在pH10和pH 5.5处进行分馏的情况。 (c)2019年作者。由elsevier b.v出版。

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