S100A1 utilizes different mechanisms for interacting with calcium-dependent and calcium-independent target proteins.

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TitleS100A1 utilizes different mechanisms for interacting with calcium-dependent and calcium-independent target proteins.
Publication TypeJournal Article
Year of Publication1998
AuthorsLandar, A, Rustandi, RR, Weber, DJ, Zimmer, DB
JournalBiochemistry
Volume37
Issue50
Pagination17429-38
Date Published1998 Dec 15
ISSN0006-2960
KeywordsAmino Acid Sequence, Amino Acid Substitution, Animals, Biological Markers, Calcium, Calcium-Binding Proteins, Cattle, Electrophoresis, Agar Gel, Enzyme Activation, Fructose-Bisphosphate Aldolase, Molecular Sequence Data, Mutagenesis, Site-Directed, Oligopeptides, Peptide Fragments, Point Mutation, Rats, Recombinant Fusion Proteins, S100 Proteins
Abstract

While previous studies have identified target proteins that interact with S100A1 in a calcium-dependent manner as well as target proteins that interact in a calcium-independent manner, the molecular mechanisms of S100A1-target protein interaction have not been elucidated. In this study, point and deletion mutants of S100A1 were used to investigate the contribution of carboxyl terminal amino acids to S100A1 interaction with calcium-dependent and calcium-independent target proteins. First, a recombinant rat S100A1 protein (recS100A1) expressed in bacteria exhibited physical and chemical properties indistinguishable from native S100A1. Next, proteins lacking the carboxyl-terminal nine residues of recS100A1 (Delta85-93), or containing alanine substitutions at Phe 88 (F88A), Phe 89 (F89A), or Trp 90 (W90A), both Phe 88 and Phe 89 (F88/89A), or all three aromatic residues (F88/89A-W90A) were recombinantly expressed. Like recS100A1, F88A, F89A, and W90A proteins interacted with phenyl-Sepharose in a calcium-dependent manner. However, the Delta85-93 protein did not interact with phenyl-Sepharose, indicating that a phenyl-Sepharose-binding region (PSBR) of recS100A1 had been disrupted. The F88/89A and F88/89A-W90A proteins exhibited reduced calcium-dependent interaction with phenyl-Sepharose when compared with recS100A1, demonstrating that the carboxyl-terminal aromatic residues Phe 88, Phe 89, and Trp 90 comprise the PSBR of S100A1. Fluorescence studies showed that the Delta85-93 protein exhibited reduced calcium-dependent interaction with the dodecyl CapZ peptide, TRTK, while W90A bound TRTK with a Kd of 5.55 microM. These results demonstrate that the calcium-dependent target protein-binding site and the PSBR are indistinguishable. In contrast to the calcium-dependent target TRTK, activation of the calcium-independent target protein aldolase A by the point and deletion mutant S100A1s was indistinguishable from native S100A1. These results demonstrate that carboxyl-terminal residues are not required for S100A1 modulation of calcium-independent target protein aldolase A. Alltogether, these results indicate that S100A1 utilizes distinct mechanisms for interaction with calcium-independent and calcium-dependent target proteins.

DOI10.1021/bi9817921
Alternate JournalBiochemistry
PubMed ID9860858
Grant ListGM 52071 / GM / NIGMS NIH HHS / United States
NS 30660 / NS / NINDS NIH HHS / United States