Design of a leucine zipper coiled coil stabilized 1.4 kcal mol-1 by phosphorylation of a serine in the e position

Protein Sci. 1997 Jun;6(6):1273-83. doi: 10.1002/pro.5560060615.

Abstract

Using a dimeric bZIP protein, we have designed a leucine zipper that becomes more stable after a serine in the e position is phosphorylated by protein kinase A (delta delta GP = -1.4 kcal mol-1 dimer-1 or -0.7 kcal mol-1 residue-1). Mutagenesis studies indicate that three arginines form a network of inter-helical (i,i' + 5; i, i' + 2) and intra-helical (i, i + 4) attractive interactions with the phosphorylated serine. When the arginines are replaced with lysines, the stabilizing effect of serine phosphorylation is reduced (delta delta GP = -0.5 kcal mol-1 dimer-1). The hydrophobic interface of the leucine zipper needs a glycine in the d position to obtain an increase in stability after phosphorylation. The phosphorylated protein binds DNA with a 15-fold higher affinity. Using a transient transfection assay, we document a PKA dependent four-fold activation of a reporter gene. Phosphorylation of a threonine in the same e position decreases the stability by delta delta GP = +1.2 kcal mol-1 dimer-1. We present circular dichroism (CD) thermal denaturations of 15 bZIP proteins before and after phosphorylation. These data provide insights into the structural determinants that result in stabilization of a coiled coil by phosphorylation.

Publication types

  • Comparative Study

MeSH terms

  • Amino Acid Sequence
  • Arginine / chemistry
  • Avian Proteins*
  • Basic-Leucine Zipper Transcription Factors
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Centrifugation, Isopycnic
  • Circular Dichroism
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • DNA Probes / metabolism
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • G-Box Binding Factors
  • Genes, Reporter
  • Glutamic Acid
  • Glycine / chemistry
  • Glycine / genetics
  • Glycine / metabolism
  • Hot Temperature
  • Leucine Zippers* / genetics
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Protein Binding
  • Protein Denaturation
  • Protein Engineering
  • Protein Structure, Secondary*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Serine / chemistry
  • Serine / genetics
  • Serine / metabolism*
  • Threonine / chemistry
  • Threonine / genetics
  • Threonine / metabolism
  • Transcription Factors / chemistry
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcriptional Activation
  • Transfection

Substances

  • Avian Proteins
  • Basic-Leucine Zipper Transcription Factors
  • Carrier Proteins
  • DNA Probes
  • DNA-Binding Proteins
  • G-Box Binding Factors
  • Phosphoproteins
  • Recombinant Proteins
  • Transcription Factors
  • Threonine
  • Glutamic Acid
  • Serine
  • Arginine
  • Cyclic AMP-Dependent Protein Kinases
  • Glycine