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F-actin affinity chromatography: technique for isolating previously unidentified actin-binding proteins.
Author(s) -
Kathryn G. Miller,
Bruce Alberts
Publication year - 1989
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.86.13.4808
Subject(s) - actin , actin binding protein , protein filament , actin cytoskeleton , cytoskeleton , affinity chromatography , actin remodeling , actina , microfilament , mdia1 , biology , biochemistry , chemistry , microbiology and biotechnology , cell , enzyme
We have developed stable and easy to use filamentous actin (F-actin) affinity-chromatography columns that selectively purify proteins that bind to actin filaments from cell extracts. Most traditional assays for actin-associated proteins screen for their effects on actin polymerization or actin filament crosslinking. Because our technique requires only actin-filament binding, it can identify additional types of proteins involved in the function of the actin cytoskeleton. By chromatographing extracts of several types of cells on these columns, we show that known actin-binding proteins are selectively retained as a subset of a larger group of actin-binding proteins that have not been identified previously.

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