A Single Mutation at the Sheet Switch Region Results in Conformational Changes Favoring lambda 6 Light-Chain Fibrillogenesis


Autoria(s): HERNANDEZ-SANTOYO, Alejandra; YAUNER, Luis del Pozo; FUENTES-SILVA, Deyanira; ORTIZ, Ernesto; RUDINO-PINERA, Enrique; SANCHEZ-LOPEZ, Rosana; HORJALES, Eduardo; BECERRIL, Baltazar; RODRIGUEZ-ROMERO, Adela
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

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

http://dx.doi.org/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