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Lab Chip. 2009 Apr 07;9(7):1014-7. doi: 10.1039/b815503h. Epub 2009 Jan 15.

When one chip is not enough: augmenting the validity of SELDI-TOF proteomic profiles of clinical specimens.

Lab on a chip

Greplova Kristina, Pilny Radomir, Budinska Eva, Dubska Lenka, Lakomy Radek, Vyzula Rostislav, Vojtesek Borivoj, Valik Dalibor

Affiliations

  1. Department of Laboratory Medicine, Masaryk Memorial Cancer Institute, Brno, Czech Republic.

PMID: 19294317 DOI: 10.1039/b815503h

Abstract

To improve recovery, selectivity and reproducibility of SELDI-TOF analyses, we found it necessary to modify manufacturer's recommended protocols on sample and chip preparation. To yield reproducible denaturing conditions we verified concentrations of denaturing, reducing and lipid-solubilizing agents. We improved sorption of molecules of interest and reproducibility of analyses by introducing the preconditioning step and alkaline/acidic elutions for normal phase chips. The ratio that reproducibly decomposed the specimen was urea 9 mol l(-1) + DTT 10 mmol l(-1) + CHAPS 20 g l(-1). For sample denaturation, 100 microl of the fresh mixture was added to 100 microl of the specimen. Our modification of a chip processing increased recovery of the NP20 chip by up to 400% as assessed by total ion current. We obtained the range of mass accuracy of 0.02-0.04% and response precision between 30-40% of m/z+. We observed about 50% peak overlap. To obtain approximately 92% of possible peaks three chip selectivities, IMAC, H50 and normal phase with alkaline wash should be used. The selectivity of the SELDI chips is affected by unspecific interactions of a sample with a chip backbone. The system is compatible with matrix-based biological materials and does not suffer from urea interference and sensitivity to covalently bound alkaline ions. The technique is reasonably suitable for semiquantitative screening in the mammalian low-molecular weight cellular, tissue and plasma proteome.

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