Truncated variants of the GCN4 transcription activator protein bind DNA with dramatically different dynamical motifs.

Abstract:

:The yeast protein GCN4 is a transcriptional activator in the basic leucine zipper (bZip) family, whose distinguishing feature is the "chopstick-like" homodimer of alpha helices formed at the DNA-binding interface. While experiments have shown that truncated versions of the protein retain biologically relevant DNA-binding affinity, we present the results of a computational study revealing that these variants show a wide variety of dynamical modes in their interaction with the target DNA sequence. We have performed all-atom molecular dynamics simulations of the full-length GCN4 protein as well as three truncated variants; our data indicate that the truncated mutants show dramatically different correlation patterns. We conclude that although the truncated mutants still retain DNA-binding ability, the bZip interface present in the full-length protein provides important stability for the protein-DNA complex.

journal_name

J Chem Inf Model

authors

McHarris DM,Barr DA

doi

10.1021/ci500448e

subject

Has Abstract

pub_date

2014-10-27 00:00:00

pages

2869-75

issue

10

eissn

1549-9596

issn

1549-960X

journal_volume

54

pub_type

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