Isotope-Coded Maleimide Affinity Tags for Proteomics Applications

Author(s):  
Adam P. Wdowiak ◽  
Marisa N. Duong ◽  
Rohan D. Joyce ◽  
Amber E. Boyatzis ◽  
Mark C. Walkey ◽  
...  
Keyword(s):  
2020 ◽  
Vol 21 (8) ◽  
pp. 821-830
Author(s):  
Vibhor Mishra

The affinity tags are unique proteins/peptides that are attached at the N- or C-terminus of the recombinant proteins. These tags help in protein purification. Additionally, some affinity tags also serve a dual purpose as solubility enhancers for challenging protein targets. By applying a combinatorial approach, carefully chosen affinity tags designed in tandem have proven to be very successful in the purification of single proteins or multi-protein complexes. In this mini-review, the key features of the most commonly used affinity tags are discussed. The affinity tags have been classified into two significant categories, epitope tags, and protein/domain tags. The epitope tags are generally small peptides with high affinity towards a chromatography resin. The protein/domain tags often perform double duty as solubility enhancers as well as aid in affinity purification. Finally, protease-based affinity tag removal strategies after purification are discussed.


2004 ◽  
Vol 76 (14) ◽  
pp. 4104-4111 ◽  
Author(s):  
Yu Lu ◽  
Patricia Bottari ◽  
Frantisek Turecek ◽  
Ruedi Aebersold ◽  
Michael H. Gelb

2006 ◽  
Vol 57 (3) ◽  
pp. 599-608 ◽  
Author(s):  
H. Peter van Esse ◽  
Bart P. H. J. Thomma ◽  
John W. van 't Klooster ◽  
Pierre J. G. M. de Wit

2010 ◽  
Vol 98 (3) ◽  
pp. 445a
Author(s):  
Nicholas D. Tingquist ◽  
Anna E. Daily ◽  
T.K.S. Kumar

2004 ◽  
Vol 126 (6) ◽  
pp. 1636-1637 ◽  
Author(s):  
Martin L. Ludwiczek ◽  
Bettina Baminger ◽  
Robert Konrat

Author(s):  
Koichi Fukase ◽  
San-Qi Zhang ◽  
Yoshiyuki Fukase ◽  
Naomi Umesako ◽  
Shoichi Kusumoto

2021 ◽  
Vol 14 (1) ◽  
pp. 363-387
Author(s):  
Bo Cheng ◽  
Qi Tang ◽  
Che Zhang ◽  
Xing Chen

As one of the major types of biomacromolecules in the cell, glycans play essential functional roles in various biological processes. Compared with proteins and nucleic acids, the analysis of glycans in situ has been more challenging. Herein we review recent advances in the development of methods and strategies for labeling, imaging, and profiling of glycans in cells and in vivo. Cellular glycans can be labeled by affinity-based probes, including lectin and antibody conjugates, direct chemical modification, metabolic glycan labeling, and chemoenzymatic labeling. These methods have been applied to label glycans with fluorophores, which enables the visualization and tracking of glycans in cells, tissues, and living organisms. Alternatively, labeling glycans with affinity tags has enabled the enrichment of glycoproteins for glycoproteomic profiling. Built on the glycan labeling methods, strategies enabling cell-selective and tissue-specific glycan labeling and protein-specific glycan imaging have been developed. With these methods and strategies, researchers are now better poised than ever to dissect the biological function of glycans in physiological or pathological contexts.


Sign in / Sign up

Export Citation Format

Share Document