Crucial role of position 40 for interactions of CCK-58 revealed by sequence of cat CCK-58 |
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Authors: | Reeve Joseph R Rosenquist Grace L Keire David A Chew Peter Nicholas Hugh B Davis Michael T Lee Terry D Shively John E Backus Robert C |
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Affiliation: | CURE: Digestive Diseases Research Center, Veterans Administration Greater Los Angeles Healthcare System, Los Angeles, CA 90073, USA. |
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Abstract: | Evidence suggests that amino terminal extensions of CCK-8 affect the carboxyl terminal bioactive region of CCK. Cat CCK-58 was purified by low pressure reverse phase and ion-exchange chromatography steps and several reverse phase HPLC steps. The purified peptide and its tryptic fragments were characterized by mass spectral analysis and microsequence analysis. The structure of cat CCK-58 is: AVQKVDGEPRAHLGALLARYIQQARKAPSGRMSVIKNLQSLDPSHRISDRDY(SO3) MGWMDF-amide. Cat and dog CCK-58 are identical except for position 40 which is serine in cat and asparagine in dog. Radioimmunoassay detected cat CCK-58 about 1/10th as well as dog CCK-58, indicating a marked effect on C-terminal immunoreactivity. Cat CCK-58 with a serine at position 40, the same residue found in pig, mouse, cow and rabbit CCK-58, can be used as a unique bioprobe for defining how amino terminal amino acids influence the structure and bioactivity of the carboxyl terminal region of CCK. |
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Keywords: | Pancreas Cholecystokinin Conformations Structure-activity relationships Sequence analysis Mass spectral analysis Molecular forms |
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