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Absolute Quantification Method for Protein Concentration
被引:13
|作者:
Li, Mingdong
[1
,2
,3
]
Tan, Jiaojie
[1
,2
,3
]
Tarlov, Michael J.
[3
]
Zachariah, Michael R.
[1
,2
,3
]
机构:
[1] Univ Maryland, Dept Chem & Biomol Engn, College Pk, MD 20742 USA
[2] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[3] NIST, Gaithersburg, MD 20899 USA
关键词:
DIFFERENTIAL MOBILITY ANALYSIS;
IONIZATION MASS-SPECTROMETRY;
ELECTROSPRAY-IONIZATION;
MECHANISM;
RANGE;
IONS;
D O I:
10.1021/ac5030123
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
A fast and accurate assay to determine the absolute concentration of proteins is described based on direct measurement of droplet entrapped oligomer formation in electrospray. Here we demonstrate the approach using electrospray differential mobility analysis (ES-DMA), which can distinguish monomers and dimers from higher order oligomers. A key feature of the method is that it allows determination of the absolute number concentration of proteins eliminating the need for protein-specific calibration. The method was demonstrated by measuring the concentration of a NIST Standard Reference Material 927e (bovine serum albumin), a high-purity immunoglobulin G 1, and a formulated Rituximab. The method may be applied to any electrospray source, regardless of diagnostic tool (e.g., MS or ion-mobility, etc.), provided the electrospray is operated in a droplet-fission mode.
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页码:12130 / 12137
页数:8
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