Biomarker discovery from the plasma proteome using multidimensional fractionation proteomics.

Abstract:

:Because biomarkers are typically low in abundance, the crucial step of biomarker discovery is to efficiently separate clinically relevant sets of proteins that might define disease stages and/or predict disease development. It is anticipated that a multi-dimensional fractionation system (MDFS) will provide an efficient means of separating low abundance proteins from plasma proteins, resulting in the extension of the detection limit. However, when using an MDFS to analyze the plasma proteome it is important to consider how sample processing, yield, resolution and throughput potential may influence the detection limit. This review evaluates the recent advances in MDFS research with respect to '4RS criterion' (4R: resolution, reproducibility, recovery, and robustness; 4S: simplicity, speed, selectivity and sensitivity) and discusses perspectives for future plasma-derived biomarker discovery.

journal_name

Curr Opin Chem Biol

authors

Lee HJ,Lee EY,Kwon MS,Paik YK

doi

10.1016/j.cbpa.2006.01.007

subject

Has Abstract

pub_date

2006-02-01 00:00:00

pages

42-9

issue

1

eissn

1367-5931

issn

1879-0402

pii

S1367-5931(06)00006-8

journal_volume

10

pub_type

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