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Abstract:

The ankyrin repeat (AR) domain of IκBα consists of a cooperative folding unit of roughly four ARs (AR1-AR4) and of two weakly folded repeats (AR5 and AR6). The kinetic folding mechanism of the cooperative subdomain, IκBα 67-206, was analyzed using rapid mixing techniques. Despite its apparent architectural simplicity, IκBα 67-206 displays complex folding kinetics, with two sequential on-pathway high-energy intermediates. The effect of mutations to or away from the consensus sequences of ARs on folding behavior was analyzed, particularly the GXTPLHLA motif, which have not been examined in detail previously. Mutations toward the consensus generally resulted in an increase in folding stability, whereas mutations away from the consensus resulted in decreased overall stability. We determined the free energy change upon mutation for three sequential transition state ensembles along the folding route for 16 mutants. We show that folding initiates with the formation of the interface of the outer helices of AR3 and AR4, and then proceeds to consolidate structure in these repeats. Subsequently, AR1 and AR2 fold in a concerted way in a single kinetic step. We show that this mechanism is robust to the presence of AR5 and AR6 as they do not strongly affect the folding kinetics. Overall, the protein appears to fold on a rather smooth energy landscape, where the folding mechanism conforms a one-dimensional approximation. However, we note that the AR does not necessarily act as a single folding element. © 2011 Elsevier Ltd.

Registro:

Documento: Artículo
Título:Folding kinetics of the cooperatively folded subdomain of the IκBα ankyrin repeat domain
Autor:Devries, I.; Ferreiro, D.U.; Sánchez, I.E.; Komives, E.A.
Filiación:Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, San Diego, CA 92093-0378, United States
Protein Physiology Laboratory, Departamento de Quimica Biologica, Universidad de Buenos Aires, C1428EGA Buenos Aires, Argentina
Consejo Nacional de Investigaciones Cientificas, Tecnicas de Argentina, C1428EGA Buenos Aires, Argentina
Palabras clave:α value; folding landscapeNFκB; protein folding; repeat protein; ankyrin; ankyrin 1; ankyrin 2; ankyrin 3; ankyrin 4; ankyrin 5; ankyrin 6; I kappa B alpha; mutant protein; unclassified drug; article; gene deletion; gene mutation; human; kinetics; priority journal; protein analysis; protein folding; protein stability; temperature; Amino Acid Sequence; Ankyrin Repeat; Ankyrins; Consensus Sequence; Humans; I-kappa B Proteins; Kinetics; Models, Molecular; Molecular Sequence Data; Mutation; Protein Folding; Sequence Homology, Amino Acid
Año:2011
Volumen:408
Número:1
Página de inicio:163
Página de fin:176
DOI: http://dx.doi.org/10.1016/j.jmb.2011.02.021
Título revista:Journal of Molecular Biology
Título revista abreviado:J. Mol. Biol.
ISSN:00222836
CODEN:JMOBA
CAS:I kappa B alpha, 151217-48-0; Ankyrins; I-kappa B Proteins
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00222836_v408_n1_p163_Devries

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Citas:

---------- APA ----------
Devries, I., Ferreiro, D.U., Sánchez, I.E. & Komives, E.A. (2011) . Folding kinetics of the cooperatively folded subdomain of the IκBα ankyrin repeat domain. Journal of Molecular Biology, 408(1), 163-176.
http://dx.doi.org/10.1016/j.jmb.2011.02.021
---------- CHICAGO ----------
Devries, I., Ferreiro, D.U., Sánchez, I.E., Komives, E.A. "Folding kinetics of the cooperatively folded subdomain of the IκBα ankyrin repeat domain" . Journal of Molecular Biology 408, no. 1 (2011) : 163-176.
http://dx.doi.org/10.1016/j.jmb.2011.02.021
---------- MLA ----------
Devries, I., Ferreiro, D.U., Sánchez, I.E., Komives, E.A. "Folding kinetics of the cooperatively folded subdomain of the IκBα ankyrin repeat domain" . Journal of Molecular Biology, vol. 408, no. 1, 2011, pp. 163-176.
http://dx.doi.org/10.1016/j.jmb.2011.02.021
---------- VANCOUVER ----------
Devries, I., Ferreiro, D.U., Sánchez, I.E., Komives, E.A. Folding kinetics of the cooperatively folded subdomain of the IκBα ankyrin repeat domain. J. Mol. Biol. 2011;408(1):163-176.
http://dx.doi.org/10.1016/j.jmb.2011.02.021