Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins

A new, easier and efficient purification method, using Sephacryl and DEAE-Sephacel, of the C-terminal fragment of two ?-macroglobulins, ?2-M and PZP, is presented. Two larger peptides were identified for each protein as the C-terminal fragment, with molecular weights of ?30 kDa and the N-terminal se...

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Autores:
Tipo de recurso:
Fecha de publicación:
2007
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22891
Acceso en línea:
https://doi.org/10.1016/j.pep.2006.12.008
https://repository.urosario.edu.co/handle/10336/22891
Palabra clave:
Alpha 2 macroglobulin
Chymotrypsin
Low density lipoprotein receptor related protein
Monoclonal antibody
Peptide fragment
Placenta protein
Proteinase
Unclassified drug
Amino acid sequence
Article
Chemistry
Enzyme linked immunosorbent assay
Female
Human
Hydrolysis
Isolation and purification
Metabolism
Molecular genetics
Molecular weight
Polyacrylamide gel electrophoresis
Pregnancy
Protein tertiary structure
Sequence analysis
Time
Western blotting
Alpha-macroglobulins
Amino acid sequence
Chymotrypsin
Endopeptidases
Enzyme-linked immunosorbent assay
Female
Humans
Hydrolysis
Ldl-receptor related protein 1
Molecular sequence data
Molecular weight
Peptide fragments
Pregnancy
Pregnancy proteins
Time factors
?-macroglobulins
C-terminal region
Chymotrypsin
Pzp
polyacrylamide gel
western
tertiary
protein
monoclonal
human
Pzp protein
Antibodies
Blotting
Electrophoresis
Protein structure
Sequence analysis
Rights
License
Abierto (Texto Completo)
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dc.title.spa.fl_str_mv Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins
title Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins
spellingShingle Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins
Alpha 2 macroglobulin
Chymotrypsin
Low density lipoprotein receptor related protein
Monoclonal antibody
Peptide fragment
Placenta protein
Proteinase
Unclassified drug
Amino acid sequence
Article
Chemistry
Enzyme linked immunosorbent assay
Female
Human
Hydrolysis
Isolation and purification
Metabolism
Molecular genetics
Molecular weight
Polyacrylamide gel electrophoresis
Pregnancy
Protein tertiary structure
Sequence analysis
Time
Western blotting
Alpha-macroglobulins
Amino acid sequence
Chymotrypsin
Endopeptidases
Enzyme-linked immunosorbent assay
Female
Humans
Hydrolysis
Ldl-receptor related protein 1
Molecular sequence data
Molecular weight
Peptide fragments
Pregnancy
Pregnancy proteins
Time factors
?-macroglobulins
C-terminal region
Chymotrypsin
Pzp
polyacrylamide gel
western
tertiary
protein
monoclonal
human
Pzp protein
Antibodies
Blotting
Electrophoresis
Protein structure
Sequence analysis
title_short Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins
title_full Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins
title_fullStr Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins
title_full_unstemmed Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins
title_sort Proteolytic hydrolysis and purification of the LRP/alfa-2-macroglobulin receptor domain from ?-macroglobulins
dc.subject.keyword.spa.fl_str_mv Alpha 2 macroglobulin
Chymotrypsin
Low density lipoprotein receptor related protein
Monoclonal antibody
Peptide fragment
Placenta protein
Proteinase
Unclassified drug
Amino acid sequence
Article
Chemistry
Enzyme linked immunosorbent assay
Female
Human
Hydrolysis
Isolation and purification
Metabolism
Molecular genetics
Molecular weight
Polyacrylamide gel electrophoresis
Pregnancy
Protein tertiary structure
Sequence analysis
Time
Western blotting
Alpha-macroglobulins
Amino acid sequence
Chymotrypsin
Endopeptidases
Enzyme-linked immunosorbent assay
Female
Humans
Hydrolysis
Ldl-receptor related protein 1
Molecular sequence data
Molecular weight
Peptide fragments
Pregnancy
Pregnancy proteins
Time factors
?-macroglobulins
C-terminal region
Chymotrypsin
Pzp
topic Alpha 2 macroglobulin
Chymotrypsin
Low density lipoprotein receptor related protein
Monoclonal antibody
Peptide fragment
Placenta protein
Proteinase
Unclassified drug
Amino acid sequence
Article
Chemistry
Enzyme linked immunosorbent assay
Female
Human
Hydrolysis
Isolation and purification
Metabolism
Molecular genetics
Molecular weight
Polyacrylamide gel electrophoresis
Pregnancy
Protein tertiary structure
Sequence analysis
Time
Western blotting
Alpha-macroglobulins
Amino acid sequence
Chymotrypsin
Endopeptidases
Enzyme-linked immunosorbent assay
Female
Humans
Hydrolysis
Ldl-receptor related protein 1
Molecular sequence data
Molecular weight
Peptide fragments
Pregnancy
Pregnancy proteins
Time factors
?-macroglobulins
C-terminal region
Chymotrypsin
Pzp
polyacrylamide gel
western
tertiary
protein
monoclonal
human
Pzp protein
Antibodies
Blotting
Electrophoresis
Protein structure
Sequence analysis
dc.subject.keyword.eng.fl_str_mv polyacrylamide gel
western
tertiary
protein
monoclonal
human
Pzp protein
Antibodies
Blotting
Electrophoresis
Protein structure
Sequence analysis
description A new, easier and efficient purification method, using Sephacryl and DEAE-Sephacel, of the C-terminal fragment of two ?-macroglobulins, ?2-M and PZP, is presented. Two larger peptides were identified for each protein as the C-terminal fragment, with molecular weights of ?30 kDa and the N-terminal sequences were determined to be SSTQDTV for ?2-M and VALHLS for PZP. The smaller peptides with molecular weights of 18 kDa correspond to a shorter C-terminal sequence of these proteins, and they were determined to be EEFPFA for ?2-M and ALKVQTV for PZP, with no interfering sequences detected. The results confirmed the discriminatory capacity of the purification procedure and the purity of the fragments. This new methodology facilitates biological studies of ?-macroglobulins, and will enable elucidation of the role the C-terminal region may exert to eliminate ?-macroglobulin-proteinases complexes from the circulation by the LRP/receptor. © 2006 Elsevier Inc. All rights reserved.
publishDate 2007
dc.date.created.spa.fl_str_mv 2007
dc.date.accessioned.none.fl_str_mv 2020-05-25T23:58:35Z
dc.date.available.none.fl_str_mv 2020-05-25T23:58:35Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.pep.2006.12.008
dc.identifier.issn.none.fl_str_mv 10960279
10465928
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/22891
url https://doi.org/10.1016/j.pep.2006.12.008
https://repository.urosario.edu.co/handle/10336/22891
identifier_str_mv 10960279
10465928
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 118
dc.relation.citationIssue.none.fl_str_mv No. 1
dc.relation.citationStartPage.none.fl_str_mv 112
dc.relation.citationTitle.none.fl_str_mv Protein Expression and Purification
dc.relation.citationVolume.none.fl_str_mv Vol. 53
dc.relation.ispartof.spa.fl_str_mv Protein Expression and Purification, ISSN:10960279, 10465928, Vol.53, No.1 (2007); pp. 112-118
dc.relation.uri.spa.fl_str_mv https://www.scopus.com/inward/record.uri?eid=2-s2.0-33847163955&doi=10.1016%2fj.pep.2006.12.008&partnerID=40&md5=9730f35888b3b2710a8328fcb7d80894
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
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