Nanotechnologies in proteomics

被引:58
作者
Ivanov, YD
Govorun, VM
Bykov, VA
Archakov, AI
机构
[1] RAMS, Inst Biomed Chem, Moscow 119121, Russia
[2] MDT, NT, Moscow, Russia
关键词
atomic-force microscopy; CD-ROM reader biosensor; nanobiotechnology; nanotechnology; optical biosensors;
D O I
10.1002/pmic.200402087
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Progress in proteomic researches is largely determined by development and implementation of Received: December 21, 2004 new methods for the revelation and identification of proteins in biological material in a wide Revised: August 1, 2005 concentration range (from 10(-3) M to single molecules). The most perspective approaches to Accepted: August 8, 2005 address this problem involve (i) nanotechnological physicochemical procedures for the separation of multicomponent protein mixtures; among these of particular interest are biospecific nanotechnological procedures for selection of proteins from multicomponent protein mixtures with their subsequent concentration on solid support; (ii) identification and counting of single molecules by use of molecular detectors. The prototypes of biospecific nanotechnological procedures, based on the capture of ligand biomolecules by biomolecules of immobilized ligate and the concentration of the captured ligands on appropriate surfaces, are well known; these are affinity chromatography, magnetic biobeads technology, different biosensor methods, etc. Here, we review the most promising nanotechnological approaches for selection of proteins and kinetic characterization of their complexes based on these biospecific methods with subsequent MS/MS identification of proteins and protein complexes. Two major groups of methods for the analysis and identification of individual molecules and their complexes by use of molecular detectors will be reviewed: scanning probe microscopy (SPM) (including atomic-force microscopy) and cryomassdetector technology.
引用
收藏
页码:1399 / 1414
页数:16
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