The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo

Journal of Biological Chemistry

Volumn 283, Issue 23, 2008, Pages 15694-15700

  Bross, Peter ^a   Naundrup, Søren ^b   Hansen, Jakob ^a   Nielsen, Marit Nyholm ^a   Christensen, Jane Hvarregaard ^a   Kruhøffer, Mogens ^a   Palmfeldt, Johan ^a   Corydon, Thomas Juhl ^c   Gregersen, Niels ^a   Ang, Debbie ^d,e   Georgopoulos, Costa ^d,e   Nielsen, Kåre Lehmann ^b  

^a AARHUS UNIVERSITY HOSPITAL   (Denmark)

^b AALBORG UNIVERSITY   (Denmark)

^c AARHUS UNIVERSITY   (Denmark)

^d UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^e UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGGLOMERATION; ANIMAL CELL CULTURE; BACTERIOLOGY; CELL GROWTH; COBALT; GENES; GROWTH (MATERIALS); GROWTH KINETICS;

AEROBIC GROWTHS; ATPASE ACTIVITIES; BACTERIAL CELL GROWTHS; DOMINANT NEGATIVES; GROWTH ARRESTS; HEREDITARY SPASTIC PARAPLEGIAS; HETEROZYGOSITY; IN VITRO; IN-VIVO; MALATE DEHYDROGENASES; METABOLIC PATHWAYS; MICROARRAY ANALYSIS; MODEL SYSTEMS; PROTEIN AGGREGATIONS;

PROTEIN FOLDING;

ADENOSINE TRIPHOSPHATASE; CHAPERONIN; HEAT SHOCK PROTEIN 10; HEAT SHOCK PROTEIN 60; MALATE DEHYDROGENASE; HSPD1 PROTEIN, HUMAN; MICROTUBULE ASSOCIATED PROTEIN;

AEROBIC BACTERIUM; ARTICLE; BACTERIAL CELL; BACTERIAL GROWTH; CONTROLLED STUDY; ENZYME ACTIVITY; ESCHERICHIA COLI; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOSITY; IN VITRO STUDY; IN VIVO STUDY; MICROARRAY ANALYSIS; MOLECULAR MECHANICS; NONHUMAN; OPERON; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN EXPRESSION; PROTEIN FOLDING; UPREGULATION; AMINO ACID SUBSTITUTION; BIOLOGICAL MODEL; GENETICS; GROWTH, DEVELOPMENT AND AGING; HETEROZYGOTE; HUMAN; METABOLISM;

BACTERIA (MICROORGANISMS);

ADENOSINE TRIPHOSPHATASES; AMINO ACID SUBSTITUTION; CHAPERONIN 10; CHAPERONINS; ESCHERICHIA COLI; HETEROZYGOTE; HUMANS; MALATE DEHYDROGENASE; MICROTUBULE-ASSOCIATED PROTEINS; MODELS, BIOLOGICAL; OPERON; PROTEIN FOLDING; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 46149118689     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M800548200     Document Type: Article

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