Literature DB >> 31606079

Biochemical and structural analysis of N-terminal acetyltransferases.

Leah Gottlieb1, Ronen Marmorstein2.   

Abstract

N-terminal acetylation is a co- and post-translational modification catalyzed by the conserved N-terminal acetyltransferase (NAT) family of enzymes. A majority of the human proteome is modified by the human NATs (NatA-F and H), which are minimally composed of a catalytic subunit and as many as two auxiliary subunits. Together, NATs specifically regulate many cellular functions by influencing protein activities such as their degradation, membrane targeting, and protein-protein interactions. This chapter will describe methods developed for their preparation, and their biochemical and structural characterization. This will include methodologies for expression and purification of recombinant NAT protein, kinetic assays, biochemical and biophysical assays, and strategies for structural studies.
© 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biophysical analysis; Co-translational acetylation; N-terminal acetyltransferases; NATs; Protein acetyltransferases; Protein complexes; X-ray crystallography

Mesh:

Substances:

Year:  2019        PMID: 31606079      PMCID: PMC6884420          DOI: 10.1016/bs.mie.2019.07.016

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


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