Abstract

Calexcitin (CE) is a calcium sensor protein that has been implicated in associative learning. The CE gene was previously cloned from the long-finned squid, Loligo pealei, and the gene product was shown to bind GTP and modulate K(+) channels and ryanodine receptors in a Ca(2+)-dependent manner. We cloned a new gene from L. pealei, which encodes a CE-like protein, here named calexcitin B (CE(B)). CE(B) has 95% amino acid identity to the original form. Our sequence analyses indicate that CEs are homologous to the sarcoplasmic calcium-binding protein subfamily of the EF-hand superfamily. Far and near UV circular dichroism and nuclear magnetic resonance studies demonstrate that CE(B) binds Ca(2+) and undergoes a conformational change. CE(B) is phosphorylated by protein kinase C, but not by casein kinase II. CE(B) does not bind GTP. Western blot experiments using polyclonal antibodies generated against CE(B) showed that CE(B) is expressed in the L. pealei optic lobe. Taken together, the neuronal protein CE represents the first example of a Ca(2+) sensor in the sarcoplasmic calcium-binding protein family.

Highlights

  • Calcium ions (Ca2ϩ) play a vital role in cells, being involved in various signaling events from cell growth to cell death

  • We found that calexcitin B (CEB) shows 28% amino acid identity to assignment of the Branchiostoma lanceolatum SCP (ASCP) [19], which is higher than the identity score

  • The sarcoplasmic calcium-binding proteins (SCPs) protein subfamily of the EF-hand superfamily comprises a number of invertebrate muscle proteins, with molecular masses ranging from 20 to 22 kDa

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Summary

The abbreviations used are

CaBP, calcium-binding protein; CD, circular dichroism; CE, calexcitin; CKII, casein kinase II; HSQC, heteronuclear single-quantum correlation; PKC, protein kinase C; SCP, sarcoplasmic calcium-binding protein; PAGE, polyacrylamide gel electrophoresis; SP, sense primer; AP, antisense primer; ASCP, B. lanceomotif, termed “EF-hand” [1]. A new CaBP called calexcitin (CE) has been identified in squid and implicated to play a role in associative learning through inhibition of Kϩ channels in a Ca2ϩ-dependent manner [3,4,5]. It was reported [6] that CE binds and activates ryanodine receptors, which are involved in associative learning [7]. We describe a new homologue of CE, termed CEB (the original form of CE (Ref. 4) is denoted CEA for clarity). The recombinant CEB has been expressed and purified from Escherichia coli and characterized using biochemical and biophysical techniques

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