Structural research on surface layers: A focus on stability, surface layer homology domains, and surface layer cell wall interactions

被引:177
作者
Engelhardt, H [1 ]
Peters, J [1 ]
机构
[1] Max Planck Inst Biochem, Abt Mol Strukturbiol, D-82152 Martinsried, Germany
关键词
electron crystallography; electron microscopy; electron tomography; surface layer proteins from Bacteria and Archaea; S-layer cell wall interactions; S-layer homology domain; S-layer structure; SLH domain; stability of S-layer proteins; high resolution structure of S-layers;
D O I
10.1006/jsbi.1998.4070
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Surface layers (S-layers) from Bacteria and Archaea are built from protein molecules arrayed in a two-dimensional lattice, forming the outermost cell wall layer in many prokaryotes. In almost half a century of S-layer research a wealth of structural, biochemical, and genetic data have accumulated, but it has not been possible to correlate sequence data with the tertiary structure of S-layer proteins to date. In this paper, some highlights of structural aspects of archaeal and bacterial S-layers that allow us to draw some conclusions on molecular properties are reviewed. We focus on the structural requirements for the extraordinary stability of many S-layer proteins, the structural and functional aspects of the S-layer homology domain found in S-layers, extracellular enzymes and related functional proteins, and outer membrane proteins, and the molecular interactions of S-layer proteins with other cell wall components. Finally, the perspectives and requirements for structural research on S-layers, which indicate that the investigation of isolated protein domains will be a prerequisite for solving S-layer structures at atomic resolution, are discussed. (C) 1998 Academic Press.
引用
收藏
页码:276 / 302
页数:27
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