Hypothermia affects translocation of numerous cytoplasmic proteins following global cerebral ischemia

Journal of Proteome Research

Volumn 6, Issue 7, 2007, Pages 2822-2832

  Teilum, Maria ^a,b   Krogh, Morten ^a   Wieloch, Tadeusz ^a   Mattiasson, Gustav ^a  

^a LUND UNIVERSITY   (Sweden)

^b BMC A13   (Sweden)

Author keywords

2D gel; Cortex; Cytoskeleton; Glycolysis; LC MS MS; MALDI; Plasticity; Redox sensitive

Indexed keywords

CYTOPLASM PROTEIN; GLYCOLYTIC ENZYME;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN ISCHEMIA; CONTROLLED STUDY; CYTOSOL; GLYCOLYSIS; HYPOTHERMIA; MALE; NERVE CELL PLASTICITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN LOCALIZATION; PROTEIN TRANSPORT; PROTEIN VARIANT; RAT; TWO DIMENSIONAL GEL ELECTROPHORESIS;

ANIMALS; BRAIN; BRAIN CHEMISTRY; CEREBRAL INFARCTION; CYTOSOL; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; HYPOTHERMIA, INDUCED; MALE; OXIDATION-REDUCTION; PROTEIN TRANSPORT; PROTEINS; PROTEOMICS; RATS; RATS, WISTAR;

RATTUS;

EID: 34547161332     PISSN: 15353893     EISSN: None     Source Type: Journal    
DOI: 10.1021/pr070057l     Document Type: Article

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73. aIPI, identity according to International Protein Index; N, number of spots assigned to protein; HT/C, hypothermia vs control ± SD; NT/C, normothermia/control ± SD; HT/NT, hypothermia/normothermia ±SD. *: Assigned if All Spots Show the Same Type of Regulation (up- or down-regulation) and if 50% of Their Individual p-values Are below 0.05. Note That for Actin and Tubulin All Isoforms Were Included in the Same Ratio. Details for Individual Spots Are Available in Table A, Supplementary Data.