Towards ultra-high peak capacities and peak-production rates using spatial three-dimensional liquid chromatography

被引:43
作者
Wouters, Bert [1 ]
Davydova, Ekaterina [2 ]
Wouters, Sam [1 ]
Vivo-Truyols, Gabriel [2 ]
Schoenmakers, Peter J. [2 ]
Eeltink, Sebastiaan [1 ]
机构
[1] Vrije Univ Brussel, Dept Chem Engn, B-1050 Brussels, Belgium
[2] Univ Amsterdam, Vant Hoff Inst Mol Sci, NL-1098 XH Amsterdam, Netherlands
关键词
INTACT PROTEINS; SEPARATIONS; PROTEOMICS; DISCOVERY; PEPTIDES; COLUMNS; DESIGN;
D O I
10.1039/c5lc01169h
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In order to successfully tackle the truly complex separation problems arising from areas such as proteomics research, the development of ultra-efficient and fast separation technology is required. In spatial three-dimensional chromatography, components are separated in the space domain with each peak being characterized by its coordinates in a three-dimensional separation body. Spatial three-dimensional (3D-) LC has the potential to offer unprecedented resolving power when orthogonal retention mechanisms are applied, since the total peak capacity is the product of the three individual peak capacities. Due to parallel developments during the second-and third-dimension separations, the analysis time is greatly reduced compared to a coupled-column multi-dimensional LC approach. This communication discusses the different design aspects to create a microfluidic chip for spatial 3D-LC. The use of physical barriers to confine the flow between the individual developments, and flow control by the use of D-2 and D-3 flow distributors is discussed. Furthermore, the in situ synthesis of monolithic stationary phases is demonstrated. Finally, the potential performance of a spatial 3D-LC systems is compared with the performance obtained with stateof- the-art 1D-LC and (coupled-column) 2D-LC approaches via a Pareto-optimization approach. The proposed microfluidic device for 3D-LC featuring 16 D-2 channels and 256 D-3 channels can potentially yield a peak capacity of 8000 in a total analysis time of 10 minutes.
引用
收藏
页码:4415 / 4422
页数:8
相关论文
共 20 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]  
[Anonymous], 1997, HDB CHEMOMETRICS Q A
[3]   Study on the performance of different types of three-dimensional chromatographic systems [J].
Davydova, Ekaterina ;
Schoenmakers, Peter J. ;
Vivo-Truyols, Gabriel .
JOURNAL OF CHROMATOGRAPHY A, 2013, 1271 :137-143
[4]   Reversed-phase liquid chromatographic separation of complex samples by optimizing temperature and gradient time I. Peak capacity limitations [J].
Dolan, JW ;
Snyder, LR ;
Djordjevic, NM ;
Hill, DW ;
Waeghe, TJ .
JOURNAL OF CHROMATOGRAPHY A, 1999, 857 (1-2) :1-20
[5]   Comparison of the efficiency of microparticulate and monolithic capillary columns [J].
Eeltink, S ;
Decrop, WMC ;
Rozing, GP ;
Schoenmakers, PJ ;
Kok, WT .
JOURNAL OF SEPARATION SCIENCE, 2004, 27 (17-18) :1431-1440
[6]   1 mm ID poly(styrene-co-divinylbenzene) monolithic columns for high-peak capacity one- and two-dimensional liquid chromatographic separations of intact proteins [J].
Eeltink, Sebastiaan ;
Dolman, Sebastiaan ;
Detobel, Frederik ;
Desmet, Gert ;
Swart, Remco ;
Ursem, Mario .
JOURNAL OF SEPARATION SCIENCE, 2009, 32 (15-16) :2504-2509
[7]   MALDI imaging mass spectrometry: Spatial molecular analysis to enable a new age of discovery [J].
Gessel, Megan M. ;
Norris, Jeremy L. ;
Caprioli, Richard M. .
JOURNAL OF PROTEOMICS, 2014, 107 :71-82
[8]   TWO-DIMENSIONAL SEPARATIONS - CONCEPT AND PROMISE [J].
GIDDINGS, JC .
ANALYTICAL CHEMISTRY, 1984, 56 (12) :1258-&
[9]   THEORETICAL INVESTIGATION OF THE POTENTIALITIES OF THE USE OF A MULTIDIMENSIONAL COLUMN IN CHROMATOGRAPHY [J].
GUIOCHON, G ;
BEAVER, LA ;
GONNORD, MF ;
SIOUFF, AM ;
ZAKARIA, M .
JOURNAL OF CHROMATOGRAPHY, 1983, 255 (JAN) :415-437
[10]   Implementations of two-dimensional liquid chromatography [J].
Guiochon, Georges ;
Marchetti, Nicola ;
Mriziq, Khaled ;
Shalliker, R. Andrew .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1189 (1-2) :109-168