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Updated: Mar 13, 2026

High-throughput Purification of Affinity-tagged Recombinant Proteins
Published on: August 26, 2012
A Synopsis of Proteins and Their Purification
Dermot Walls1,2, Gary Cooney3,4, Sinéad T Loughran5
1School of Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland. dermot.walls@dcu.ie.
Abstract:
The isolation of a given protein, free of all other biomolecules, is the primary objective of any protein purification scheme. Classical chromatographic procedures have been designed to exploit particular distinguishing features of individual target proteins, such as size, physicochemical properties, and binding affinity. Advances in molecular biology and bioinformatics have positively contributed at every level to the challenge of purifying individual proteins and more recently have led to the development of high-throughput proteomic platforms. Here, a synopsis of developments in the field of protein chromatography is given, with reference to the principal tools and resources that are available to assist with protein purification processes.
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