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AFM fishing nanotechnology is the way to reverse the Avogadro number in proteomics

Future development of proteomics may be hindered by limitations in the concentration sensitivity of widespread technological approaches. The concentration sensitivity limit (CSL) of currently used approaches, like 2‐DE/LC separation coupled with MS detection, etc., varies from 10−9 to 10−12 M. There...

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Published in:Proteomics (Weinheim) 2007-01, Vol.7 (1), p.4-9
Main Authors: Archakov, Alexander Ivanovich, Ivanov, Yurii Dmitrievich, Lisitsa, Andrey Valerevich, Zgoda, Victor Gavrilovich
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description Future development of proteomics may be hindered by limitations in the concentration sensitivity of widespread technological approaches. The concentration sensitivity limit (CSL) of currently used approaches, like 2‐DE/LC separation coupled with MS detection, etc., varies from 10−9 to 10−12 M. Therefore, proteomic technologies enable detection of up to 20% of the protein species present in the plasma. New technologies, like atomic force microscopy (AFM molecular detector), enable the counting of single molecules, whereas biospecific fishing can be used to capture these molecules from the biomaterial. At the same time, fishing also has thermodynamic limitations due to the reversibility of the binding. In cases where the fishing becomes irreversible, its combination with an AFM detector enables the registration of single protein molecules, and that opens up a way to lower the CSL down to the reverse Avogadro number.
doi_str_mv 10.1002/pmic.200600467
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subjects Atomic-force microscopy
Biospecific fishing
Microscopy, Atomic Force - instrumentation
Microscopy, Atomic Force - methods
Molecular detectors
Nanobiotechnology
Nanotechnology
Proteomics
Sensitivity and Specificity
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
title AFM fishing nanotechnology is the way to reverse the Avogadro number in proteomics
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