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Measurement of Noncovalent Complexes with High m/z by Electrospray Time-of-Flight Mass Spectrometry

Identifieur interne : 000903 ( Istex/Corpus ); précédent : 000902; suivant : 000904

Measurement of Noncovalent Complexes with High m/z by Electrospray Time-of-Flight Mass Spectrometry

Auteurs : I. V. Chernushevich ; W. Ens ; K. G. Standing

Source :

RBID : ISTEX:14CDBCD173F9D463E751FEE12F04EB8E35641A68

Abstract

Abstract: In the last few years the electrospray (ES) ionization technique has proved to be gentle enough to obtain information on the higher-order structure of biomolecules [1]. However, most ES-MS studies with proteins have been carried out in acidic solutions. Such acidic solutions, particularly in combination with organic solvents, denature biopolymers, which then acquire sufficient charge to be detected within the limited m/z range of most commercial quadrupole mass spectrometers. These conditions are usually sufficiently severe so as to destroy any higher order structure, which must be examined closer to physiological conditions. There the charge acquired may be much lower, resulting in m/z values beyond the range of normal quadrupole instruments (see for example [2]).

Url:
DOI: 10.1007/978-94-015-9046-4_8

Links to Exploration step

ISTEX:14CDBCD173F9D463E751FEE12F04EB8E35641A68

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<Para>In the last few years the electrospray (ES) ionization technique has proved to be gentle enough to obtain information on the higher-order structure of biomolecules [1]. However, most ES-MS studies with proteins have been carried out in acidic solutions. Such acidic solutions, particularly in combination with organic solvents, denature biopolymers, which then acquire sufficient charge to be detected within the limited
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<abstract lang="en">Abstract: In the last few years the electrospray (ES) ionization technique has proved to be gentle enough to obtain information on the higher-order structure of biomolecules [1]. However, most ES-MS studies with proteins have been carried out in acidic solutions. Such acidic solutions, particularly in combination with organic solvents, denature biopolymers, which then acquire sufficient charge to be detected within the limited m/z range of most commercial quadrupole mass spectrometers. These conditions are usually sufficiently severe so as to destroy any higher order structure, which must be examined closer to physiological conditions. There the charge acquired may be much lower, resulting in m/z values beyond the range of normal quadrupole instruments (see for example [2]).</abstract>
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