Antifreeze proteins (AFPs) are found in many marine fish and have been classified into five biochemical classes: AFP types I-IV and the antifreeze glycoproteins. Type I AFPs are ␣-helical, partially amphipathic, Alarich polypeptides. The winter flounder (Pleuronectes americanus) produces two type I AFP subclasses, the liver-type AFPs (wflAFPs) and the skin-type AFPs (wfsAFPs), that are encoded by distinct gene families with different tissue-specific expression. wfsAFPs and wflAFPs share a high level of identity even though the wfsAFPs have approximately half the activity of the wflAFPs. Synthetic polypeptides based on two representative wflAFPs and wfsAFPs were generated to examine the role of the termini in antifreeze activity. Through systematic exchange of N and C termini between wflAFP-6 and wfsAFP-2, the termini were determined to be the major causative agents for the variation in activity levels between the two AFPs. Furthermore, the termini of wflAFP-6 possessed greater helix-stabilizing ability compared with their wfsAFP-2 counterparts. The observed 50% difference in activity between wflAFP-6 and wfsAFP-2 can be divided into ϳ20% for differences at each termini and ϳ10% for differences in the core. Furthermore, the N terminus was determined to be the most critical component for antifreeze activity.Fish antifreeze proteins are diverse in structure and have been grouped into five biochemical classes based on their structural characteristics: antifreeze proteins (AFPs) 1 types I-IV and antifreeze glycoproteins (AFGPs) (1-3). Although diverse in structure, all AF(G)Ps act by what is known as the adsorption inhibition mechanism (2, 4 -6), where the AF(G)Ps lower the observed freezing point in a non-colligative manner creating a hysteresis between the equilibrium melting point and the observed freezing point. The degree of thermal hysteresis is used as a measure of AF(G)P activity.Type I AFPs are Ala-rich, partially amphipathic single ␣-helical polypeptides found in several sculpins and righteye flounders (2,7,8). The winter flounder (Pleuronectes americanus) produces two subclasses of type I AFPs, the liver-type (wflAFPs) and the skin-type AFPs (wfsAFPs), which are encoded by distinct gene families (9). wflAFP-6 (formerly known as HPLC-6) is the major winter flounder plasma AFP and is produced in the liver as a prepro-precursor, and then secreted into circulation, where it is then processed into the mature polypeptide of 37 residues (10, 11). Conversely, the wfsAFPs have a wider tissue distribution and are produced as mature intracellular polypeptides (9).The wflAFPs and wfsAFPs share a high level of structural identity even though the wfsAFPs have approximately half the activity of wflAFP-6 (9). Both wflAFPs and wfsAFPs possess two 11-residue motifs of the structure TaaXAXXAAXX (where the first Thr is always conserved, uppercase A is a conserved Ala, lowercase a is almost always Ala, and X can be one of several amino acids), with wflAFP-6 having a third full motif at the N terminus (see Fig. 1). Furthermore,...