Published in

International Union of Crystallography, Acta Crystallographica Section F: Structural Biology Communications, 9(72), p. 677-680, 2016

DOI: 10.1107/s2053230x16011638

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Surface-layer protein fromCaulobacter crescentus: expression, purification and X-ray crystallographic analysis

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Data provided by SHERPA/RoMEO

Abstract

Protein surface layers are self-assembling, paracrystalline lattices on the surface of many prokaryotes. Surface-layer proteins have not benefited from widespread structural analysis owing to their resistance to crystallization. Here, the successful expression of a truncated version of RsaA, the surface-layer protein fromCaulobacter crescentus, from aCaulobacterprotein-expression system is reported. The purification, crystallization and initial X-ray diffraction analysis of the truncated RsaA, the largest surface-layer protein studied to date and the first from a Gram-negative bacterium, are also reported.