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

被引:210
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
相关论文
共 33 条
  • [1] Host Protein Biomarkers Identify Active Tuberculosis in HIV Uninfected and Co-infected Individuals
    Achkar, Jacqueline M.
    Cortes, Laetitia
    Croteau, Pascal
    Yanofsky, Corey
    Mentinova, Marija
    Rajotte, Isabelle
    Schirm, Michael
    Zhou, Yiyong
    Junqueira-Kipnis, Ana Paula
    Kasprowicz, Victoria O.
    Larsen, Michelle
    Allard, Rene
    Hunter, Joanna
    Paramithiotis, Eustache
    [J]. EBIOMEDICINE, 2015, 2 (09): : 1160 - 1168
  • [2] MStern Blotting-High Throughput Polyvinylidene Fluoride (PVDF) Membrane-Based Proteomic Sample Preparation for 96-Well Plates
    Berger, Sebastian T.
    Ahmed, Saima
    Muntel, Jan
    Polo, Nerea Cuevas
    Bachur, Richard
    Kentsis, Alex
    Steen, Judith
    Steen, Hanno
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2015, 14 (10) : 2814 - 2823
  • [3] Large-Scale Label-Free Quantitative Mapping of the Sputum Proteome
    Burg, Dominic
    Schofield, James P. R.
    Brandsma, Joost
    Staykova, Doroteya
    Folisi, Caterina
    Bansal, Aruna
    Nicholas, Ben
    Xian, Yang
    Rowe, Anthony
    Corfield, Julie
    Wilson, Susan
    Ward, Jonathan
    Lutter, Rene
    Fleming, Louise
    Shaw, Dominick E.
    Bakke, Per S.
    Caruso, Massimo
    Dahlen, Sven-Erik
    Fowler, Stephen J.
    Hashimoto, Simone
    Horvath, Ildiko
    Howarth, Peter
    Krug, Norbert
    Montuschi, Paolo
    Sanak, Marek
    Sandstrom, Thomas
    Singer, Florian
    Sun, Kai
    Pandis, Ioannis
    Auffray, Charles
    Sousa, Ana R.
    Adcock, Ian M.
    Chung, Kian Fan
    Sterk, Peter J.
    Djukanovic, Ratko
    Skipp, Paul J.
    [J]. JOURNAL OF PROTEOME RESEARCH, 2018, 17 (06) : 2072 - 2091
  • [4] Comparative Study of Workflows Optimized for In-gel, In-solution, and On-filter Proteolysis in the Analysis of Plasma Membrane Proteins
    Choksawangkarn, Waeowalee
    Edwards, Nathan
    Wang, Yan
    Gutierrez, Peter
    Fenselau, Catherine
    [J]. JOURNAL OF PROTEOME RESEARCH, 2012, 11 (05) : 3030 - 3034
  • [5] Enhanced FASP (eFASP) to Increase Proteome Coverage and Sample Recovery for Quantitative Proteomic Experiments
    Erde, Jonathan
    Loo, Rachel R. Ogorzalek
    Loo, Joseph A.
    [J]. JOURNAL OF PROTEOME RESEARCH, 2014, 13 (04) : 1885 - 1895
  • [6] Proteomic Challenges: Sample Preparation Techniques for Microgram-Quantity Protein Analysis from Biological Samples
    Feist, Peter
    Hummon, Amanda B.
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2015, 16 (02) : 3537 - 3563
  • [7] The Orosomucoid 1 protein is involved in the vitamin D - mediated macrophage de-activation process
    Gemelli, Claudia
    Martello, Andrea
    Montanari, Monica
    Marani, Tommaso Zanocco
    Salsi, Valentina
    Zappavigna, Vincenzo
    Parenti, Sandra
    Vignudelli, Tatiana
    Selmi, Tommaso
    Ferrari, Sergio
    Grande, Alexis
    [J]. EXPERIMENTAL CELL RESEARCH, 2013, 319 (20) : 3201 - 3213
  • [8] Ultra-deep and quantitative saliva proteome reveals dynamics of the oral microbiome
    Grassl, Niklas
    Kulak, Nils Alexander
    Pichler, Garwin
    Geyer, Philipp Emanuel
    Jung, Jette
    Schubert, Soeren
    Sinitcyn, Pavel
    Cox, Juergen
    Mann, Matthias
    [J]. GENOME MEDICINE, 2016, 8
  • [9] Assessment of Sample Preparation Bias in Mass Spectrometry-Based Proteomics
    Klont, Frank
    Bras, Linda
    Wolters, Justina C.
    Ongay, Sara
    Bischoff, Rainer
    Halmos, Gyorgy B.
    Horvatovich, Peter
    [J]. ANALYTICAL CHEMISTRY, 2018, 90 (08) : 5405 - 5413
  • [10] The discovery and identification of a candidate proteomic biomarker of active tuberculosis
    Liu, Jiyan
    Jiang, Tingting
    Wei, Liliang
    Yang, Xiuyun
    Wang, Chong
    Zhang, Xing
    Xu, Dandan
    Chen, Zhongliang
    Yang, Fuquan
    Li, Ji-Cheng
    [J]. BMC INFECTIOUS DISEASES, 2013, 13