Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

A label-free MALDI TOF MS-based method for studying the kinetics and inhibitor screening of the Alzheimer's disease drug target β-secretase

M. Machálková, J. Schejbal, Z. Glatz, J. Preisler,

. 2018 ; 410 (28) : 7441-7448. [pub] 20180915

Language English Country Germany

Document type Journal Article

E-resources Online Full text

NLK ProQuest Central from 2011-01-01 to 1 year ago
Medline Complete (EBSCOhost) from 2003-01-01 to 1 year ago
Health & Medicine (ProQuest) from 2011-01-01 to 1 year ago

Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI TOF MS) is a well-established method with a unique set of qualities including sensitivity, minute sample consumption, and label-free detection, all of which are highly desired in enzyme assays. On the other hand, the application of MALDI TOF MS is usually limited by high concentrations of MS-incompatible compounds in the reaction mixture such as salts or organic solvents. Here, we introduce kinetic and inhibition studies of β-secretase (BACE1), a key enzyme of the progression of Alzheimer's disease. Compatibility of the enzyme assay with MALDI TOF MS was achieved, providing both a complex protocol including a desalting step designed for rigorous kinetic studies and a simple mix-and-measure protocol designed for high-throughput inhibitor screening. In comparison with fluorescent or colorimetric assays, MALDI TOF MS represents a sensitive, fast, and label-free technique with minimal sample preparation. In contrast to other MS-based methodological approaches typically used in drug discovery processes, such as a direct injection MS or MS-coupled liquid chromatography or capillary electrophoresis, MALDI TOF MS enables direct analysis and is a highly suitable approach for high-throughput screening. The method's applicability is strongly supported by the high correlation of the acquired kinetic and inhibition parameters with data from the literature as well as from our previous research. Graphical abstract ᅟ.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc19012376
003      
CZ-PrNML
005      
20190405101606.0
007      
ta
008      
190405s2018 gw f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s00216-018-1354-6 $2 doi
035    __
$a (PubMed)30218128
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gw
100    1_
$a Machálková, Markéta $u Department of Analytical Chemistry, Faculty of Science, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic. Central European Institute of Technology (CEITEC), Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic.
245    12
$a A label-free MALDI TOF MS-based method for studying the kinetics and inhibitor screening of the Alzheimer's disease drug target β-secretase / $c M. Machálková, J. Schejbal, Z. Glatz, J. Preisler,
520    9_
$a Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI TOF MS) is a well-established method with a unique set of qualities including sensitivity, minute sample consumption, and label-free detection, all of which are highly desired in enzyme assays. On the other hand, the application of MALDI TOF MS is usually limited by high concentrations of MS-incompatible compounds in the reaction mixture such as salts or organic solvents. Here, we introduce kinetic and inhibition studies of β-secretase (BACE1), a key enzyme of the progression of Alzheimer's disease. Compatibility of the enzyme assay with MALDI TOF MS was achieved, providing both a complex protocol including a desalting step designed for rigorous kinetic studies and a simple mix-and-measure protocol designed for high-throughput inhibitor screening. In comparison with fluorescent or colorimetric assays, MALDI TOF MS represents a sensitive, fast, and label-free technique with minimal sample preparation. In contrast to other MS-based methodological approaches typically used in drug discovery processes, such as a direct injection MS or MS-coupled liquid chromatography or capillary electrophoresis, MALDI TOF MS enables direct analysis and is a highly suitable approach for high-throughput screening. The method's applicability is strongly supported by the high correlation of the acquired kinetic and inhibition parameters with data from the literature as well as from our previous research. Graphical abstract ᅟ.
650    _2
$a Alzheimerova nemoc $x enzymologie $7 D000544
650    _2
$a aminokyseliny $x antagonisté a inhibitory $7 D000596
650    _2
$a sekretasy $x antagonisté a inhibitory $x metabolismus $7 D053829
650    _2
$a preklinické hodnocení léčiv $x metody $7 D004353
650    _2
$a HEK293 buňky $7 D057809
650    _2
$a heterocyklické sloučeniny bicyklické $x farmakologie $7 D006574
650    _2
$a lidé $7 D006801
650    _2
$a kinetika $7 D007700
650    _2
$a kyseliny pikolinové $x farmakologie $7 D010848
650    _2
$a pyrimidinony $x farmakologie $7 D011744
650    _2
$a spektrometrie hmotnostní - ionizace laserem za účasti matrice $x metody $7 D019032
655    _2
$a časopisecké články $7 D016428
700    1_
$a Schejbal, Jan $u Department of Biochemistry, Faculty of Science, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic.
700    1_
$a Glatz, Zdeněk $u Department of Biochemistry, Faculty of Science, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic.
700    1_
$a Preisler, Jan $u Department of Analytical Chemistry, Faculty of Science, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic. preisler@chemi.muni.cz. Central European Institute of Technology (CEITEC), Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic. preisler@chemi.muni.cz.
773    0_
$w MED00006638 $t Analytical and bioanalytical chemistry $x 1618-2650 $g Roč. 410, č. 28 (2018), s. 7441-7448
856    41
$u https://pubmed.ncbi.nlm.nih.gov/30218128 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20190405 $b ABA008
991    __
$a 20190405101615 $b ABA008
999    __
$a ok $b bmc $g 1391686 $s 1050681
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2018 $b 410 $c 28 $d 7441-7448 $e 20180915 $i 1618-2650 $m Analytical and bioanalytical chemistry $n Anal Bioanal Chem $x MED00006638
LZP    __
$a Pubmed-20190405

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...