The crystal structure of Drosophila NLP-core provides insight into pentamer formation and histone binding

Structure. 2003 Feb;11(2):175-86. doi: 10.1016/s0969-2126(03)00007-8.

Abstract

The nucleoplasmin-like protein from Drosophila (dNLP) functions as a chaperone for core histones and may remodel chromatin in embryos. We now report the crystal structure of a dNLP-core pentamer at 1.5 A resolution. The monomer has an eight-stranded, beta barrel topology that is similar to nucleoplasmin (Np). However, a signature beta hairpin is tucked in along the lateral surface of the dNLP-core pentamer, while it extends outward in the Np-core decamer. Drosophila NLP and Np both assemble histone octamers. This process may require each chaperone to form a decamer, which would create symmetric binding sites for the histones. Conformational differences between dNLP and Np may reflect their different oligomeric states, while a conserved, nonpolar subunit interface may allow conformational plasticity during histone binding.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Crystallography, X-Ray
  • Drosophila / chemistry*
  • Drosophila / metabolism
  • Histones / chemistry
  • Histones / metabolism*
  • Molecular Sequence Data
  • Nuclear Proteins / chemistry*
  • Nuclear Proteins / metabolism
  • Nucleocytoplasmic Transport Proteins*
  • Sequence Alignment
  • Temperature

Substances

  • Histones
  • NUP42 protein, human
  • Nuclear Proteins
  • Nucleocytoplasmic Transport Proteins

Associated data

  • PDB/1NLQ