PURIFICATION AND CHARACTERIZATION OF 2 POTENT HEAT-STABLE PROTEIN INHIBITORS OF PROTEIN PHOSPHATASE 2A FROM BOVINE KIDNEY

被引:203
作者
LI, M [1 ]
GUO, H [1 ]
DAMUNI, Z [1 ]
机构
[1] PENN STATE UNIV, COLL MED, MILTON S HERSHEY MED CTR, DEPT CELLULAR & MOLEC PHYSIOL, HERSHEY, PA 17033 USA
关键词
D O I
10.1021/bi00006a020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two heat-stable protein inhibitors of protein phosphatase 2A (PP2A), tentatively designated I-1(PP2A) and I-2(PP2A), have been purified to apparent homogeneity from extracts of bovine kidney. The purified preparations of I-1(PP2A) exhibited an apparent M(r) similar to 30 000 and 250 000 as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and gel permeation chromatography on Sephacryl S-300, respectively. In contrast, the purified preparations of I-2(PP2A) exhibited an apparent M(r) similar to 20 000 and 80 000 as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and gel permeation chromatography on Sephacryl S-200, respectively. The purified preparations of I-1(PP2A) and I-2(PP2A) inhibited PP2A with P-32-labeled myelin basic protein, P-32-labeled histone H1, P-32-labeled pyruvate dehydrogenase complex, P-32-labeled phosphorylase, and protamine kinase as substrates. By contrast, I-1(PP2A) and I-2(PP2A) exhibited little effect, if any, on the activity of PP2A with P-32-labeled casein, and did not prevent the autodephosphorylation of PP2A in incubations with the autophosphorylation-activated protein kinase [Guo, H., and Damuni, Z. (1993) Proc. Natl. Acad. Sci. U.S.A. 90, 2500-2504]. The purified preparations of I-1(PP2A) and I-2(PP2A) had little effect, if any, on the activities of protein phosphatase 1, protein phosphatase 2B, protein phosphatase 2C, and pyruvate dehydrogenase phosphatase. With P-32-labeled MBP as a substrate, kinetic analysis according to Henderson showed that I-1(PP2A) and I-2(PP2A) were noncompetitive and displayed a K-i of about 30 and 25 nM, respectively. Following cleavage with Staphylococcus aureus V8 protease, I-1(PP2A) and I-2(PP2A) displayed distinct peptide patterns, indicating that these inhibitor proteins are the products of distinct genes. The N-terminal amino acid sequences of the purified preparations indicate that I-1(PP2A) and I-2(PP2A) are novel proteins.
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页码:1988 / 1996
页数:9
相关论文
共 55 条
[1]   DEPHOSPHORYLATION OF THE HUMAN LYMPHOCYTE-T CD3 ANTIGEN [J].
ALEXANDER, D ;
GORIS, J ;
MARAIS, R ;
ROTHBARD, J ;
MERLEVEDE, W ;
CRUMPTON, MJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 181 (01) :55-65
[2]   PROTEIN PHOSPHATASE-2A IS A SPECIFIC PROTAMINE-KINASE-INACTIVATING PHOSPHATASE [J].
AMICK, GD ;
REDDY, SAG ;
DAMUNI, Z .
BIOCHEMICAL JOURNAL, 1992, 287 :1019-1022
[3]  
AMICK GD, 1992, ARCH BIOCHEM BIOPHYS, V297, P80, DOI 10.1016/0003-9861(92)90643-B
[4]   HUMAN-LIVER PHOSPHATASE 2A - CDNA AND AMINO-ACID SEQUENCE OF 2 CATALYTIC SUBUNIT ISOTYPES [J].
ARINO, J ;
CHEE, WW ;
BRAUTIGAN, DL ;
MILLER, TB ;
JOHNSON, GL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (12) :4252-4256
[5]   CHARACTERIZATION OF GLYCOGEN-SYNTHASE PHOSPHATASE AND PHOSPHORYLASE-PHOSPHATASE IN SUBCELLULAR LIVER FRACTIONS [J].
BOLLEN, M ;
VANDENHEEDE, JR ;
GORIS, J ;
STALMANS, W .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 969 (01) :66-77
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]  
BRAUTIGAN DL, 1986, J BIOL CHEM, V261, P4924
[8]  
CHEN J, 1994, J BIOL CHEM, V269, P7957
[9]   REGULATION OF PROTEIN SERINE-THREONINE PHOSPHATASE TYPE-2A BY TYROSINE PHOSPHORYLATION [J].
CHEN, J ;
MARTIN, BL ;
BRAUTIGAN, DL .
SCIENCE, 1992, 257 (5074) :1261-1264
[10]  
CHEN SC, 1989, J BIOL CHEM, V264, P7267