Literature DB >> 19892185

Theory and use of hydrophobic interaction chromatography in protein purification applications.

Justin T McCue1.   

Abstract

Hydrophobic interaction chromatography (HIC) is a valuable tool used in protein purification applications. HIC is used in the purification of proteins over a broad range of scales-in both analytical and preparatory scale applications. HIC is used to remove various impurities that may be present in the solution, including undesirable product-related impurities. In particular, HIC is often employed to remove product aggregate species, which possess different hydrophobic properties than the target monomer species and can often be effectively removed using HIC. In this chapter, we provide a description of the basic theory of HIC and how it is used to purify proteins in aqueous-based solutions. Following the theoretical background, the latest in HIC adsorbent technology is described, including a list of commonly used and commercially available adsorbents. The basic procedures for using HIC adsorbents are described next, in order to provide the reader with useful starting points to apply HIC in protein purification applications.

Mesh:

Substances:

Year:  2009        PMID: 19892185     DOI: 10.1016/S0076-6879(09)63025-1

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  8 in total

1.  Automated hydrophobic interaction chromatography column selection for use in protein purification.

Authors:  Patrick J M Murphy; Orrin J Stone; Michelle E Anderson
Journal:  J Vis Exp       Date:  2011-09-21       Impact factor: 1.355

2.  Use of tandem affinity-buffer exchange chromatography online with native mass spectrometry for optimizing overexpression and purification of recombinant proteins.

Authors:  Stella M Lai; Pankajavalli Thirugnanasambantham; Vaishnavi Sidharthan; Andrew S Norris; Jamison D Law; Venkat Gopalan; Vicki H Wysocki
Journal:  Methods Enzymol       Date:  2021-09-23       Impact factor: 1.682

3.  Native Reversed-Phase Liquid Chromatography: A Technique for LCMS of Intact Antibody-Drug Conjugates.

Authors:  Tse-Hong Chen; Yun Yang; Zhaorui Zhang; Cexiong Fu; Qunying Zhang; Jon D Williams; Mary J Wirth
Journal:  Anal Chem       Date:  2019-02-06       Impact factor: 6.986

4.  Analysis of Tagged Proteins Using Tandem Affinity-Buffer Exchange Chromatography Online with Native Mass Spectrometry.

Authors:  Florian Busch; Zachary L VanAernum; Stella M Lai; Venkat Gopalan; Vicki H Wysocki
Journal:  Biochemistry       Date:  2021-06-08       Impact factor: 3.321

5.  Semi-automated hydrophobic interaction chromatography column scouting used in the two-step purification of recombinant green fluorescent protein.

Authors:  Orrin J Stone; Kelly M Biette; Patrick J M Murphy
Journal:  PLoS One       Date:  2014-09-25       Impact factor: 3.240

Review 6.  Different Stationary Phase Selectivities and Morphologies for Intact Protein Separations.

Authors:  A Astefanei; I Dapic; M Camenzuli
Journal:  Chromatographia       Date:  2016-09-23       Impact factor: 2.044

7.  PolyBall: A new adsorbent for the efficient removal of endotoxin from biopharmaceuticals.

Authors:  Sidharth Razdan; Jee-Ching Wang; Sutapa Barua
Journal:  Sci Rep       Date:  2019-06-20       Impact factor: 4.379

8.  Improved Production and Biophysical Analysis of Recombinant Silicatein-α.

Authors:  Emily I Sparkes; Rachel A Kettles; Chisom S Egedeuzu; Natalie L Stephenson; Stephanie A Caslin; S Yasin Tabatabaei Dakhili; Lu Shin Wong
Journal:  Biomolecules       Date:  2020-08-20
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.