Effects of column length, particle size, gradient length and flow rate on peak capacity of nano-scale liquid chromatography for peptide separations

被引:61
作者
Liu, Hongji [1 ]
Finch, Jeffrey W. [1 ]
Lavallee, Michael J. [1 ]
Collamati, Robert A. [1 ]
Benevides, Christopher C. [1 ]
Gebler, John C. [1 ]
机构
[1] Waters Corp, Life Sci R&D, Milford, MA 01757 USA
关键词
peak capacity; nanoLC; column length; particle size; gradient length; flow rate; peptide;
D O I
10.1016/j.chroma.2007.02.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The effects of the column length, the particle size, the gradient length and the flow rate of a nanoLC system on peptide peak capacity were investigated and compared. Columns packed with 1.7 mu m and 3 mu m C-18 materials into pieces of 75 mu m capillary tubing of various lengths were tested with different gradient lengths and flow rates. While increasing the length of a column packed with the 1.7 mu m material helped improve peptide peak capacity at the whole range of the tested gradient lengths (24-432 min), little improvement in peak capacity was observed with the increase of the length of a column packed with the 3 mu m material unless a gradient longer than 50 min was carried out. Up to 30% of peak capacity increase was observed when a column's length is doubled, with little reduction in the throughput. In most cases, more than 50% of the increase in peak capacity was obtained with the reduction in the particle size from 3 l km to 1.7 p,m. With the same backpressure generated, a shorter 1.7-mu m-particle column outperformed a longer column packed with the 3 mu m material. In a flow rate range of 100-700 nl/min, increasing the flow rate improved peak capacity for columns packed with 1.7 mu m and 3 mu m materials. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:30 / 36
页数:7
相关论文
共 34 条
[1]   Rapid peptide mapping by reversed-phase liquid chromatography on nonporous silica with on-line electrospray time of flight mass spectrometry [J].
Banks, JF ;
Gulcicek, EE .
ANALYTICAL CHEMISTRY, 1997, 69 (19) :3973-3978
[2]   TRYPTIC PEPTIDE-MAPPING OF UBIQUITIN AND DERIVATIVES USING REVERSE-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
COX, MJ ;
SHAPIRA, R ;
WILKINSON, KD .
ANALYTICAL BIOCHEMISTRY, 1986, 154 (01) :345-352
[3]  
DALLALIBERA L, 1983, J CHROMATOGR, V264, P164
[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]   FACTORS INFLUENCING THE PERFORMANCE OF PEPTIDE-MAPPING BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
DONG, MW ;
TRAN, AD .
JOURNAL OF CHROMATOGRAPHY, 1990, 499 :125-139
[6]   ISOLATION AND COMPARATIVE PEPTIDE-MAPPING OF FIBRINOGEN SUBUNITS BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
EBERT, RF ;
SCHMELZER, CH .
JOURNAL OF CHROMATOGRAPHY, 1988, 443 :309-316
[7]   RP-HPLC PEPTIDE-MAPPING METHODS FOR THE ANALYSIS OF RECOMBINANT HUMAN PROUROKINASE [J].
FACCHETTI, I ;
VALLA, A ;
VIGEVANI, A .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1993, 11 (08) :737-744
[8]  
FULLMER CS, 1979, J BIOL CHEM, V254, P7208
[10]   Implications of column peak capacity on the separation of complex peptide mixtures in single- and two-dimensional high-performance liquid chromatography [J].
Gilar, M ;
Daly, AE ;
Kele, M ;
Neue, UD ;
Gebler, JC .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1061 (02) :183-192