S-Trap, an Ultrafast Sample-Preparation Approach for Shotgun Proteomics

被引:223
作者
HaileMariam, Milkessa [1 ,2 ]
Eguez, Rodrigo Vargas [1 ]
Singh, Harinder [1 ]
Bekele, Shiferaw [1 ,3 ]
Ameni, Gobena [2 ]
Pieper, Rembert [1 ]
Yu, Yanbao [1 ]
机构
[1] J Craig Venter Inst, 9605 Med Ctr Dr, Rockville, MD 20850 USA
[2] Addis Ababa Univ, Aklilu Lemma Inst Pathobiol, Addis Ababa, Ethiopia
[3] Univ Maryland, Med Ctr, Baltimore, MD 21201 USA
关键词
proteomics; sample preparation; FASP; suspension trapping; Klebsiella pneumoniae; sputum; tuberculosis; ACTIVE TUBERCULOSIS; PROTEIN-ANALYSIS; DIGESTION; BIOMARKERS; WORKFLOWS; INFECTION; DATABASE; PLATES; URINE; FASP;
D O I
10.1021/acs.jproteome.8b00505
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The success of shotgun proteomic analysis depends largely on how samples are prepared. Current approaches (such as those that are gel-, solution-, or filter based), although being extensively employed in the field, are time-consuming and less effective with respect to the repetitive sample processing, recovery, and overall yield. As an alternative, the suspension trapping (S-Trap) filter has been commercially available very recently in the format of a single or 96-well filter plate. In contrast to the conventional filter-aided sample preparation (FASP) approach, which utilizes a molecular weight cut-off (MWCO) membrane as the filter and requires hours of processing before digestion-ready proteins can be obtained, the S-Trap employs a three-dimensional porous material as filter media and traps particulate protein suspensions with the subsequent depletion of interfering substances and in-filter digestion. Due to the large (submicron) pore size, each centrifugation cycle of the S-Trap filter only takes 1 min, which significantly reduces the total processing time from approximately 3 h by FASP to less than 15 min, suggesting an ultrafast sample-preparation approach for shotgun proteomics. Here, we comprehensively evaluate the performance of the individual S-Trap filter and 96-well filter plate in the context of global protein identification and quantitation using whole-cell lysate and clinically relevant sputum samples.
引用
收藏
页码:2917 / 2924
页数:8
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