Miniaturized parallel screens to identify chromatographic steps required for recombinant protein purification

Kaushal Rege, Meng Heng

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Methods development in chromatography is a time-consuming, trial-and-error process that requires laborious experimentation. We describe a high-throughput screening (HTS) protocol for the rapid identification of chromatographic steps for protein purification from cell-free expression broths. Broths containing the protein are loaded on different chromatographic resins aliquotted in membrane-bottomed microtiter plates. Serial step elution of protein from resins results in fraction collection in 96-well plates. Choice of the optimal chromatographic operating conditions is based on protein purity in eluted fractions, determined using SDS-PAGE analysis or similar analytical techniques. The screening procedure is then repeated in order to identify the subsequent chromatographic steps, ultimately leading to high purities of the protein. The protocol takes ∼24 h in order to determine the required sequence of chromatographic steps. The use of a miniaturized screen facilitates screening of a range of media and operating conditions (i.e., pH, salt concentration, and so on.) in parallel and is a novel approach to chromatographic methods development.

Original languageEnglish (US)
Pages (from-to)408-417
Number of pages10
JournalNature Protocols
Volume5
Issue number3
DOIs
StatePublished - Mar 2010

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Recombinant Proteins
Purification
Screening
Proteins
Resins
Chromatography
Polyacrylamide Gel Electrophoresis
Salts
Throughput
Membranes

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Miniaturized parallel screens to identify chromatographic steps required for recombinant protein purification. / Rege, Kaushal; Heng, Meng.

In: Nature Protocols, Vol. 5, No. 3, 03.2010, p. 408-417.

Research output: Contribution to journalArticle

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