BIOLOGICALLY-ACTIVE CALCITONIN ANALOGS WHICH HAVE MINIMAL INTERACTIONS WITH PHOSPHOLIPIDS

被引：25

作者：

EPAND, RM ^{[1
]}

EPAND, RF ^{[1
]}

ORLOWSKI, RC ^{[1
]}

机构：

[1] ARMOUR PHARMACEUT CO,KANKAKEE,IL 60901

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1988年 / 152卷 / 01期

关键词：

D O I：

10.1016/S0006-291X(88)80700-9

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：

引用

页码：203 / 207

页数：5

共 10 条

[1] CONFORMATIONAL FLEXIBILITY AND BIOLOGICAL-ACTIVITY OF SALMON-CALCITONIN [J].

EPAND, RM ;

EPAND, RF ;

ORLOWSKI, RC ;

SEYLER, JK ;

COLESCOTT, RL .

BIOCHEMISTRY, 1986, 25 (08) :1964-1968

[2]

EPAND RM, 1986, INT J PEPT PROT RES, V27, P501

[3]

EPAND RM, 1987, J BIOL CHEM, V262, P9389

[4] EFFECT OF ELECTROSTATIC REPULSION ON THE MORPHOLOGY AND THERMOTROPIC TRANSITIONS OF ANIONIC PHOSPHOLIPIDS [J].

EPAND, RM ;

HUI, SW .

FEBS LETTERS, 1986, 209 (02) :257-260

[5] INTERACTION OF GLUCAGON WITH DIMYRISTOYL GLYCEROPHOSPHOCHOLINE [J].

EPAND, RM ;

JONES, AJS ;

SCHREIER, S .

BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 491 (01) :296-304

[6]

EPAND RM, 1987, PROTIDES BIOL FLUIDS, V35, P481

[7] BIOLOGICAL AND PHYSICAL-PROPERTIES OF A MODEL CALCITONIN CONTAINING A GLUTAMATE RESIDUE INTERRUPTING THE HYDROPHOBIC FACE OF THE IDEALIZED AMPHIPHILIC ALPHA-HELICAL REGION [J].

GREEN, FR ;

LYNCH, B ;

KAISER, ET .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (23) :8340-8344

[8] STUDIES OF PEPTIDE CONFORMATION IN THE DESIGN OF PEPTIDE AGONISTS [J].

KAISER, ET .

BIOCHEMICAL PHARMACOLOGY, 1987, 36 (06) :783-788

[9] BIOLOGICALLY POTENT ANALOGS OF SALMON-CALCITONIN WHICH DO NOT CONTAIN AN N-TERMINAL DISULFIDE-BRIDGED RING STRUCTURE [J].

ORLOWSKI, RC ;

EPAND, RM ;

STAFFORD, AR .

EUROPEAN JOURNAL OF BIOCHEMISTRY, 1987, 162 (02) :399-402

[10] DES-SER2 SALMON-CALCITONIN - A BIOLOGICALLY POTENT SYNTHETIC ANALOG [J].

SCHWARTZ, KE ;

ORLOWSKI, RC ;

MARCUS, R .

ENDOCRINOLOGY, 1981, 108 (03) :831-835

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