A Single Mutation at the Sheet Switch Region Results in Conformational Changes Favoring lambda 6 Light-Chain Fibrillogenesis
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2010
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Resumo |
Systemic amyloid light-chain (LC) amyloidosis is a disease process characterized by the pathological deposition of monoclonal LCs in tissue. All LC subtypes are capable of fibril formation although lambda chains, particularly those belonging to the lambda 6 type, are overrepresented. Here, we report the thermodynamic and in vitro fibrillogenic properties of several mutants of the lambda 6 protein 6aJL2 in which Pro7 and/or His8 was substituted by Ser or Pro. The H8P and H8S mutants were almost as stable as the wildtype protein and were poorly fibrillogenic. In contrast, the P7S mutation decreased the thermodynamic stability of 6aJL2 and greatly enhanced its capacity to form amyloid-like fibrils in vitro. The crystal structure of the P7S mutant showed that the substitution induced both local and long-distance effects, such as the rearrangement of the V(L) (variable region of the light chain)-V(L) interface. This mutant crystallized in two orthorhombic polymorphs, P2(1)2(1)2(1) and C222(1). In the latter, a monomer that was not arranged in the typical Bence-Jones dimer was observed for the first time. Crystal-packing analysis of the C222(1) lattice showed the establishment of intermolecular beta-beta interactions that involved the N-terminus and beta-strand B and that these could be relevant in the mechanism of LC fibril formation. Our results strongly suggest that Pro7 is a key residue in the conformation of the N-terminal sheet switch motif and, through long-distance interactions, is also critically involved in the contacts that stabilized the V(L) interface in lambda 6 LCs. (C) 2009 Elsevier Ltd. All rights reserved. Direccion General de Asuntos del Personal Academico-Universidad Nacional Autonoma de Mexico (UNAM)[IN 209506-3] Direccion General de Asuntos del Personal Academico-Universidad Nacional Autonoma de Mexico (UNAM) Direccion General de Asuntos del Personal Academico-Universidad Nacional Autonoma de Mexico (UNAM)[IN220707-3] Direccion General de Asuntos del Personal Academico-Universidad Nacional Autonoma de Mexico (UNAM) Consejo Nacional de Ciencia y Tecnología (CONACYT) - México Consejo Nacional de Ciencia y Tecnologia[82947] Consejo Nacional de Ciencia y Tecnologia (CONACYT)[D44122Q] Consejo Nacional de Ciencia y Tecnología (CONACYT) - México National Institute of General Medical Sciences (NIGMS/NIH)[0080] U.S. National Institutes of Health (NIH) U.S. Department of Energy (DOE) U.S. Department of Energy (DOE)[DE-AC02-98CH10886] |
Identificador |
JOURNAL OF MOLECULAR BIOLOGY, v.396, n.2, p.280-292, 2010 0022-2836 http://producao.usp.br/handle/BDPI/30145 10.1016/j.jmb.2009.11.038 |
Idioma(s) |
eng |
Publicador |
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD |
Relação |
Journal of Molecular Biology |
Direitos |
restrictedAccess Copyright ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD |
Palavras-Chave | #AL amyloidosis #crystal structure #fibrillogenesis #lambda 6 subgroup #thermodynamic stability #LINEAR EXTRAPOLATION METHOD #AMYLOID FIBRIL FORMATION #CROSS-BETA SPINE #AL AMYLOIDOSIS #PROTEIN #STABILITY #SOFTWARE #CRYSTALLOGRAPHY #THERMODYNAMICS #AGGREGATION #Biochemistry & Molecular Biology |
Tipo |
article original article publishedVersion |