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SAXSMoW 3.0: New advances in the determination of the molecular weight of proteins in dilute solutions from SAXS intensity data on a relative scale

dc.contributor.authorde Oliveira Neto, Mario [UNESP]
dc.contributor.authorde Freitas Fernandes, Adriano
dc.contributor.authorPiiadov, Vassili
dc.contributor.authorCraievich, Aldo Felix
dc.contributor.authorde Araújo, Evandro Ares
dc.contributor.authorPolikarpov, Igor
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionBrazilian Center for Research in Energy and Materials
dc.date.accessioned2022-04-28T19:47:17Z
dc.date.available2022-04-28T19:47:17Z
dc.date.issued2022-01-01
dc.description.abstractSAXSMoW (SAXS Molecular Weight) is an online platform widely used over the past few years for determination of molecular weights of proteins in dilute solutions. The scattering intensity retrieved from small-angle X-ray scattering (SAXS) raw data is the sole input to SAXSMoW for determination of molecular weights of proteins in liquid. The current updated SAXSMoW version 3.0 determines the linear dependence of the true protein volume on their apparent protein volume, based on SAXS curves calculated for 67,000 protein structures selected from the Protein Data Bank. SAXSMoW 3.0 was tested against 43 experimental SAXS scattering curves from proteins with known molecular weights. Our results demonstrate that most of the molecular weights determined for the nonglycosylated and also for the glycosylated proteins are in good agreement with their expected molecular weights. Additionally, the average discrepancies between the calculated molecular weights and their nominal values for glycosylated proteins are similar to those for nonglycosylated ones.en
dc.description.affiliationBiophysics and Pharmacology Department Bioscience Institute Universidade Estadual Paulista, São Paulo
dc.description.affiliationSao Carlos Institute of Physics University of Sao Paulo
dc.description.affiliationDepartment of Applied Physics University of Sao Paulo, São Paulo
dc.description.affiliationBrazilian Synchrotron Light Laboratory Brazilian Center for Research in Energy and Materials, São Paulo
dc.description.affiliationUnespBiophysics and Pharmacology Department Bioscience Institute Universidade Estadual Paulista, São Paulo
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdCNPq: 140739/2017-3
dc.description.sponsorshipIdFAPESP: 2015/13684-0
dc.description.sponsorshipIdFAPESP: 2018/22300-0
dc.description.sponsorshipIdCNPq: 303988/2016-9
dc.description.sponsorshipIdCNPq: 307490/2019-0
dc.description.sponsorshipIdCNPq: 310531/2019-5
dc.format.extent251-258
dc.identifierhttp://dx.doi.org/10.1002/pro.4227
dc.identifier.citationProtein Science, v. 31, n. 1, p. 251-258, 2022.
dc.identifier.doi10.1002/pro.4227
dc.identifier.issn1469-896X
dc.identifier.issn0961-8368
dc.identifier.scopus2-s2.0-85119419331
dc.identifier.urihttp://hdl.handle.net/11449/222891
dc.language.isoeng
dc.relation.ispartofProtein Science
dc.sourceScopus
dc.titleSAXSMoW 3.0: New advances in the determination of the molecular weight of proteins in dilute solutions from SAXS intensity data on a relative scaleen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0001-9496-4174[6]

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