BETA THYMOSIN FRAGMENTS

Description

REFERENCE TO A SEQUENCE LISTING

The present application includes a Sequence Listing filed in electronic format. The Sequence Listing is entitled “2600-258_SequenceListing.txt” created on Feb. 4, 2013, and is 2512 bytes in size. The information in the electronic format of the Sequence Listing is part of the present application and is incorporated herein by reference in its entirety.

BACKGROUND

1. Technical Field

The present disclosure relates to the field of beta thymosin fragments.

2. Description of the Background Art

Thymosin β4 was initially identified as a protein that is up-regulated during endothelial cell migration and differentiation in vitro. Thymosin β4 (Tβ4) was originally isolated from the thymus and is a 43 amino acid, 4.9 kDa ubiquitous polypeptide identified in a variety of tissues. Several roles have been ascribed to this protein including a role in endothelial cell differentiation and migration, T cell differentiation, actin sequestration and vascularization.

The amino acid sequence of Tβ4 is disclosed in U.S. Pat. No. 4,297,276, herein incorporated by reference. The gene encoding for Tβ4 was highly conserved during evolution. In fact, total homology exists between mice, rat and human Tβ4. Total homology is predicted to exist between the dog and human Tβ4 based on the analysis of a canine cDNA library.

Tβ4 has been found to be present in numerous tissue types in mammals and has also been implicated in a wide variety of cellular and physiological processes including inducing terminal deoxynucleotidyl transferase activity of bone marrow cells, stimulating secretion of hypothalamic luteinizing hormone releasing hormone and luteinizing hormone, inhibiting migration and enhancing antigen presentation of macrophages, and inducing phenotypic changes in T-cell lines in vitro.

There is a need in the art for active beta thymosin fragments.

SUMMARY OF THE INVENTION

In accordance with one embodiment, a peptide fragment having an amino acid sequence corresponding to a portion of a thymosin beta 4, a thymosin beta 10 and/or a thymosin beta 15 amino acid sequence, comprises, consists essentially of, or consists of amino acid sequence H-Leu-Lys-Lys-Thr-Glu-Thr, H-Ser-Asp-Lys-Pro, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser, H-Leu-Lys-Lys-Thr-Glu-Thr-Gln, Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr, Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser, Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu -Lys- Lys-Thr-Glu-Thr-Gln, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys, Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser, a methionine-containing variant of said fragment in which said methionine is oxidized or superoxidized, a variant of said fragment which normally is methionine-containing but which has an amino acid substituent substituted for at least one methionine of the normally methionine-containing fragment, an isolated R-enantiomer of said fragment, an isolated S-enantiomer of said fragment, or a combination thereof.

DETAILED DESCRIPTION

Beta thymosin fragments in accordance with the present invention can be provided by any suitable method, such as by solid phase peptide synthesis, one example of which is disclosed in U.S. Pat. No. 5,512,656.

Many Tβ4 isoforms have been identified and have about 70%, or about 75%, or about 80% or more homology to the known amino acid sequence of Tβ4. Such isoforms include, for example, Tβ4^ala, Tβ9, Tβ10, Tβ11, Tβ12, Tβ13, Tβ14 and Tβ15. Similar to Tβ4, the Tβ10 and Tβ15 isoforms have been shown to sequester actin. Tβ4, and many of its isoforms share an amino acid sequence, LKKTET or LKKTNT, that appears to be involved in mediating actin sequestration or binding.

According to one embodiment, a peptide fragment is provided, having an amino acid sequence corresponding to a portion of a thymosin beta 4, a thymosin beta 10 and/or a thymosin beta 15 amino acid sequence, said fragment comprising, consisting essentially of, or consisting of amino acid sequence H-Leu-Lys-Lys-Thr-Glu-Thr, H-Ser-Asp-Lys-Pro, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser, H-Leu-Lys-Lys-Thr-Glu-Thr-Gln, Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr, Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser, Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys, Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser, a methionine-containing variant of said fragment in which said methionine is oxidized or superoxidized, a variant of said fragment which normally is methionine-containing but which has an amino acid substituent substituted for at least one methionine of the normally methionine-containing fragment, an isolated R-enantiomer of said fragment, an isolated S-enantiomer of said fragment, or a combination thereof. A normally methionine-containing variant of said fragment may correspond to a methionine-containing fragment, but has an amino acid substituent substituted for at least one methionine of the fragment. Whenever herein amino acid Met is identified, it is to be understood that said Met may be substituted with amino acid AAA, wherein AAA may comprise leucine, valine, isoleucine, alanine, phenylalanine, proline or the like, substituted for said methionine.

Many beta thymosin peptides and fragments thereof include in their amino acid sequences the amino acid methionine, which is subject to oxidation in vivo and in vitro. In many of the known beta thymosins, methionine is present at position 6.

The oxidation of amino acid, methionine (C₅H₁₁NO₂S), to methionine sulfoxide (C₅H₁₁NO₃S), or otherwise, represents a major degradation pathway of methionine-containing beta thymosins such as Tp4 and fragments thereof.

Exemplary beta thymosins containing methionine at position 6 include Tβ4, Tβ4^ala, Tβ4^xen, Tβ10 and Tβ13.

In preferred embodiments, the amino acid substituted for methionine is neutral, non-polar, hydrophobic and/or non-oxidizing.

The compositions have advantages in greater stability than methionine-containing beta thymosins, while possessing activity substantially the same as, or different from the corresponding beta thymosin fragment.

In preferred embodiments, the amino acid being substituted for methionine inhibits oxidation of the beta thymosin fragment, and most preferably, the biological activity of the substituted beta thymosin fragment is substantially the same as that of the corresponding methionine-containing beta thymosin fragment.

Replacement of methionine in a methionine-containing beta thymosin peptide fragment may result in a change in the stability profile of the peptide, and/or unexpectantly new or unchanged properties of the peptide fragment.

As non-limiting examples, the amino acid to be substituted for methionine in the methionine-containing beta thymosin fragment is valine, isoleucine, alanine, phenylalanine, proline or leucine.

In accordance with one embodiment, the amino acid to be substitute for methionine in the methionine-containing beta thymosin fragment is other than leucine. In certain embodiments, the amino acid to be substituted for methionine in the methionine-containing beta thymosin is valine, isoleucine, alanine, phenylalanine or proline.

In accordance with one embodiment, the preferred amino acid to be substituted for methionine is valine or isoleucine.

In accordance with another embodiment, the preferred amino acid to be substituted for methionine is alanine.

In accordance with a still further embodiment, the preferred amino acid to be substituted for methionine is valine.

Beta thymosin fragments and variants thereof in accordance with the present invention can be provided by any suitable method, such as by solid phase peptide synthesis, one example of which is disclosed in U.S. Pat. No. 5,512,656.

PCT publication number WO 2006/076523 A1 discloses test results showing activity of Met-substituted beta thymosin peptides.

The invention also is applicable to combinations of fragments disclosed herein, which may be formed by admixing two or more different fragments (a physical mixing), or by chemically linking two or more different fragments using any suitable linkage method.

According to one embodiment, the fragment comprises amino acid sequence Ac-Leu-Lys-Lys-Thr-Glu-Thr-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Ser-Asp-Lys-Pro-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH.

According to one embodiment, the fragment comprises amino acid sequence Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-OH.

According to one embodiment, the fragment comprises amino acid sequence Ac-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH.

According to one embodiment, the fragment comprises amino acid sequence Ac-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH.According to one embodiment, the fragment comprises amino acid sequence Ac-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH.

According to one embodiment, the fragment comprises amino acid sequence Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-OH.

According to one embodiment, the fragment comprises amino acid sequence Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH.

According to one embodiment, the fragment comprises amino acid sequence Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-OH.

According to one embodiment, the fragment comprises amino acid sequence Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH.

According to one embodiment, the fragment comprises amino acid sequence H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH.

According to one embodiment, a peptide fragment is provided, having an amino acid sequence corresponding to a portion of a thymosin beta 4 amino acid sequence, said fragment comprising, consisting essentially of, or consisting of amino acid sequence H-Leu-Lys-Lys-Thr-Glu-Thr-OH.

According to one embodiment, the invention comprises a method of at least one of suppressing inflammation in tissue of a subject, stimulating cell migration in tissue of a subject, protecting tissue from cytotoxicity in tissue of a subject, inhibiting apoptosis in tissue of a subject, stimulating collagen in tissue of a subject, inhibiting collagen in tissue of a subject, stimulating collagen IV in tissue of a subject, stimulating elastin in tissue of a subject, inhibiting the activation of NFkB and its translocation in tissue of a subject, promoting neurite outgrowth, promoting neuron survival, stimulating production of L1, inhibiting tissue damage caused by ultraviolet (UV) radiation, protecting tissue from ultraviolet (UV) radiation damage, inhibiting IKBa phosphorylation in tissue of a subject, or restoring impaired T-lymphocyte blastogenic response comprising administering to said subject a peptide fragment having an amino acid sequence corresponding to a portion of a thymosin beta 4 amino acid sequence, said fragment comprising, consisting essentially of, or consisting of amino acid sequence H-Leu-Lys-Lys-Thr-Glu-Thr-OH, Ac-Leu-Lys-Lys-Thr-Glu-Thr-OH, H-Ser-Asp-Lys-Pro-OH, H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH, Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH, H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH, Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH, H-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-OH, Ac-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-OH, H-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH, Ac-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH, H-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH, Ac-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH, H-Leu-Lys-Lys-Thr-Glu-Thr, Ac-Leu-Lys-Lys-Thr-Glu-Thr, H-Ser-Asp-Lys-Pro, H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser, Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser, H-Leu-Lys-Lys-Thr-Glu-Thr-Gln, Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln, H-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr, Ac-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr, H-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser, Ac-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser, H-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser, Ac-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser, Leu-Lys-Lys-Thr-Glu-Thr-OH, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH, Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH, Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-OH, Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH, Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH, H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-OH, Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-OH, H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH, Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH, H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-OH, Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-OH, H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH, Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH, H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr, Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr, H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln, Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln, H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys, Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys, H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser, Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-OH, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH, Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-OH, Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH, a methionine-containing variant of said fragment in which said methionine is oxidized (sulfoxide) or superoxidized (sulfone), a variant of said fragment which normally is methionine-containing but which has an amino acid substituent substituted for at least one methionine of the normally methionine-containing fragment, an isolated R-enantiomer of said fragment, an isolated S-enantiomer of said fragment, or a combination thereof.

In one embodiment, the disclosure provides a method of treatment for treating, preventing, inhibiting or reducing disease, damage, injury and/or wounding of a subject, or of tissue of a subject, by administering an effective amount of a composition which contains a peptide as described herein or a combination of peptides described herein. The administering may be directly or systemically. Examples of direct administration include, for example, contacting tissue, by direct application, intrathecal injection or inhalation, with a carrier comprising a solution, lotion, salve, gel, cream, paste, spray, suspension, colloid, colloidal suspension, mix of nanoparticles, aerosol droplets, dispersion, emulsion, hydrogel, ointment, or oil including a peptide as described herein. Systemic administration includes, for example, oral, intravenous, intraperitoneal, subcutaneous, intramuscular injections of a composition containing a peptide as described herein, in a pharmaceutically acceptable carrier such as water for injection or protective chitosan nanoparticle bundles. The subject preferably is mammalian, most preferably human.

Compositions, as described herein, may be administered in any suitable effective amount. For example, a composition as described herein may be administered in dosages within the range of about 0.0001-5,000,000 micrograms, more preferably in amounts within the range of about 0.01-50,000 micrograms, most preferably within the range of about 1-500 micrograms.

A composition as described herein can be administered daily, every other day, every other week, every other month, etc., with a single application or multiple applications per day of administration, such as applications 2, 3, 4 or more times per day of administration.

The disclosure also includes a pharmaceutical or cosmetic composition comprising a therapeutically effective amount of a composition as described herein in a pharmaceutically or cosmetically acceptable carrier. Such carriers include any suitable carrier, including those listed herein.

The approaches described herein involve various routes of administration or delivery of a composition as described herein, including any conventional administration techniques (for example, but not limited to, direct administration, local injection, inhalation, or systemic administration), to a subject. The methods and compositions using or containing a composition as described herein may be formulated into pharmaceutical or cosmetic compositions by admixture with pharmaceutically acceptable or cosmetically non-toxic excipients, additives or carriers or by incorporation or linkage of a composition to a carrier or chaperone molecule to allow for targeted delivery of a composition described herein to a preferred site in the body of a mammal or preferably man.

EXAMPLES

In the examples herein, the tested fragments are identified as follows:

Fragment 1a

H-Leu-Lys-Lys-Thr-Glu-Thr-OH

Fragment 1b

Ac-Leu-Lys-Lys-Thr-Glu-Thr-OH

Fragment 2a

H-Ser-Asp-Lys-Pro-OH

Fragment 2b

Ac-Ser-Asp-Lys-Pro-OH

Fragment 3a

H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-

Phe-Asp-Lys-Ser-OH

Fragment 3b

Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-

Lys-Phe-Asp-Lys-Ser-OH

Fragment 4a

H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH

Fragment 4b

Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH

Fragment 5a

H-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-OH

Fragment 5b

Ac-Glu-Lys-Asn-Pro-Leu-Pro-Ser-Lys-Glu-Thr-OH

Fragment 6a

H-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH

Fragment 6b

Ac-Ile-Glu-Gln-Glu-Lys-Gln-Ala-Gly-Glu-Ser-OH

Fragment 7a

H-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH

Fragment 7b

Ac-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH

Fraction Aa:

H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-

Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-OH.

Fraction Ab:

Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-

Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-OH.

Fraction Ba:

H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-

Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-

Gln-OH.

Fraction Bb:

Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-

Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-

Gln-OH.

Fraction Ca:

H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-

Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-Thr-

Gln-Glu-Lys-OH.

Fraction Cb:

Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-

Lys-Phe-Asp-Lys-Ser-Lys-Leu-Lys-Lys-Thr-Glu-

Thr-Gln-Glu-Lys-OH.

Fraction Da:

H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-

Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-

Gln-Ala-Gly-Glu-Ser-OH.

Fraction Db:

Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-Glu-Lys-Asn-Pro-

Leu-Pro-Ser-Lys-Glu-Thr-Ile-Glu-Gln-Glu-Lys-

Gln-Ala-Gly-Glu-Ser-OH.

LDH Cytotoxicity Assay

- Primary passaged human dermal fibroblasts (Fb, Cascade Biologics, OR) were cultured to 80% confluence
- 2 ml chlorhexidene digluconate (CHX, 0.002%) in basal medium±1 μg/ml Tb4 or peptides was added to Fb for 1, 2, 3, or 4 hours
- 100 μl culture medium (n=4) was added to 100 μl LDH reagent and incubated at room temperature for 20 minutes
- OD500 nm was read and averages±SEM were calculated
- Data was analyzed with probability of p≦0.05

Tb4 and peptide 3A and 3B protect Fb against the cytotoxic effects of 0.002% CHX after a 2 hour exposure

Tb4 and peptide 3A protect Fb against the cytotoxic effects of 0.002% CHX after 1, 2, or 3 hours exposure

Peptide 3A protects Fb against the cytotoxic effects of 0.002% and 0.005% CHX after 2 hours exposure

Dose Response Analysis of Peptide 3A

- Human dermal fibroblasts (Fb, Cascade Biologics, OR) were cultured to 80% confluence
- 2 ml CHX (0.002%) in basal medium±1 μg/ml Tb4 or 1.0, 0.1, 0.01, or 0.001 μg/ml peptide 3A was added to Fb for 1, 2, 3, or 4 hours
- 100 μl culture medium (n=4) was added to 100 μl LDH reagent and incubated at room temperature for 20 minutes
- OD500 nm was read and averages±SEM were calculated
- Data was analyzed with probability of p≦0.05

1.0 μg/ml peptide 3A protects Fb against the cytotoxic effects of 0.002% CHX after 2 hours

Ability of Peptide 3A to Protect Against Other Cytotoxic Agents

- Human dermal fibroblasts (Fb, Cascade Biologics, OR) were cultured to 80% confluence
- 2 ml 10% ethanol, 1% hydrogen peroxide, or 0.01% benzalkonium chloride in basal medium±1 μg/ml Tb4 or 1.0, 0.1, 0.01, or 0.001 μg/ml peptide 3A was added to Fb for 1, 2, 3, or 4 hours
- 100 μl culture medium (n=4) was added to 100 μl LDH reagent and incubated at room temperature for 20 minutes
- OD500 nm was read and averages±SEM were calculated
- Data was analyzed with probability of p≦0.05

Peptide 3A does not protect Fb against the cytotoxic effects of 10% ethanol

Peptide 3A protects Fb against the cytotoxic effects of 1% hydrogen peroxide

Peptide 3A protects Fb against the cytotoxic effects of 0.01% benzalkonium chloride

Cellular Mechanisms of Cytotoxicity

Chlorhexidine: CHX can release iron from ferritin, an iron storage protein, in a dose-dependent manner which might be related to mitochondrial permeability transition

Ethanol: Some reports indicate that iron is involved in ethanol-induced cytotoxicity

Hydrogen Peroxide: The principal mechanism of H2O2 toxicity is thought to involve the generation of hydroxyl radicals through its interactions with Fe2+ ions

Benzalkonium chloride: The mechanisms of cytotoxicity of H2O2 and BAK appeared to differ

Effect of Tb4 and Peptide 3A on CHX-induced apoptosis

- Human dermal Fb were cultured to 80% confluence
- Fb were treated with 0.002% CHX+1 μg/ml Tb4 or peptide 3A, 4A or 6A for 1.5 hours
- APOPercentage “dye” was added to the Fb cultures at a 1:50 dilution for an additional 30 minutes
- Excess dye was washed from the cells, and digital images were captured. Cells dyed red were apoptotic
- Adobe Photoshop was used to calculate the number of red pixels in six digitized images for each treatment
- Statistical analysis was done using the t-test

Tb4 and peptide 3A protect Fb against apoptosis induced by exposure to 0.002% CHX for 2 hours

Peptide 3A protects Gingival Fb against cytotoxicity induced by 0.002% CHX

Tb4 and Peptide 3A protect gingival Fb against apoptosis induced by exposure to 0.002% CHX for 2 hours

Summary of Cytoxicity and Apoptosis Studies

- Peptide 3A can inhibit chlorhexidine digluconate, hydrogen peroxide, and benzalkonium chloride-induced cytotoxicity in cultured human dermal fibroblasts for up to 4 hours exposure
- Peptide 3A can inhibit chlorhexidine digluconate-induced apoptosis in cultured human dermal fibroblasts
- Peptide 3A can inhibit chlorhexidine digluconate and Peridex (diluted to 0.002% CHX) induced cytotoxicity in cultured human gingival fibroblasts
- Peptide 3A can inhibit chlorhexidine digluconate-induced apoptosis in cultured human gingival fibroblasts

Effect of Tb4 and peptides on collagen type IV secretion

- Transformed human corneal epithelial cells (HCET) were cultured to 80% confluence
- Cells were treated with 1 μg/ml Tb4 or peptides for 24 hours
- Culture supernatant samples (n=3 per experiment, total of 4 experiments) were analyzed using a collagen type IV ELISA
- Data was analyzed using the t-test

Peptides 2A and 4A stimulate collagen type IV secretion in corneal epithelial cells

Effect of Tb4 and peptides on collagen secretion

- Human dermal fibroblasts (Fb) were cultured to 80% confluence
- Cells were treated with 1 μg/ml Tb4 or peptides for 24, 48, or 72 hours. Cells were treated once/day.
- Culture supernatants (n=3, experiments repeated 5 times) were assayed for collagen secretion using a colorimetric assay that detects collagen types I, II, III, IV and V, and possibly VII

Peptide 5B stimulates the secretion of collagens by human dermal fibroblasts after 3 days of treatment

Peptides inhibit the secretion of collagens by human dermal fibroblasts

Effect of Tb4 and peptides on elastin secretion

- Human dermal fibroblasts (Fb) were cultured to 80% confluence
- Cells were treated with 1 μg/ml Tb4 or peptides for 24, 48, or 72 hours. Cells were treated once/day.
- Culture supernatants (n=3, experiments repeated 6 times) were assayed for elastin secretion using a colorimetric assay
- Data was analyzed using the t-test

Tb4 and peptides 4A, 4B, and 7B stimulate the secretion of elastin by dermal Fb

Summary of Collagen and Elastin Studies

- Peptides 2A and 4A stimulate collagen IV secretion by corneal epithelial cells
- No peptides stimulate collagen type I secretion by dermal fibroblasts
- Peptide 5B stimulates the secretion of “collagens” by dermal fibroblasts, but the type of collagen is unknown
- Peptide 4A stimulates the secretion of elastin by dermal fibroblasts

Analysis of IL-8 Secretion

- Human corneal epithelial cells or dermal Fb were cultured to 80% confluence
- Cells were pre-treated with 1 μg/ml Tb4 or peptides for one hour
- Cells were stimulated with 10 ng/ml TNF-a in the presence or absence of Tb4 or peptides
- Culture medium was analyzed for secreted IL-8 by ELISA (n=3, experiments repeated twice)
- Data was analyzed using the t-test

Tb4 and Peptide 1A suppress TNF-a-stimulated IL8 secretion in corneal epithelial cells

Tb4 and Peptides 2B and 3A suppress TNF-a-stimulated IL8 secretion in dermal fibroblasts

Analysis of NFkB Nuclear Translocation

- Human corneal epithelial cells were cultured to 80% confluence
- Cells were pre-treated with 1 μg/ml Tb4 or peptide 4A or 6A for one hour
- Cells were stimulated with 10 ng/ml TNF-a in the presence or absence of Tb4 or peptides for 15 minutes
- Cells were fixed and labeled with antibodies to the p65 subunit of NFkB

Analysis of Filamentous Actin Distribution

- Human corneal epithelial cells were cultured to 80% confluence
- Cells were pre-treated with Tb4 (1, 5, or 10 μg/ml) or peptide 4A or 6A (1 μg/ml ) for one hour
- Cells were stimulated with 10 ng/ml TNF-a in the presence or absence of Tb4 or peptides for 1 hour
- Cells were fixed and labeled with FITC-phalloidin

Effect of Tb4 and peptides on the NFkB signaling pathway

- Cell-free assay
- Prepared 1.0, 0.1, and 0.01 ng/ml solutions of Tb4 or peptides in kinase buffer supplied with kit
- Added 10 μl of the solutions to wells of a 96-well plate coated with IkBa
- IKKb (20 mU) was added to wells
- 90 μl kinase reaction buffer (containing ATP) was added to the wells
- ELISA to detect phosphorylated IkBa

Peptide 6B may have an effect on the NFkB signaling pathway by inhibiting IkBa phosphorylation.

In a further embodiment, Fragments 1 a, 1 b, 2a, 2b, 3a, 3b, 4a, 4b, 5a, 5b, 6a, 6b, 7a, and 7b are utilized to inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neurite outgrowth, promote neuron survival, and stimulate production of L1.

In one embodiment, Fragment Aa stimulates cell migration in tissue of a subject, protect tissue from cytotoxicity in tissue of a subject, inhibit apoptosis in tissue of a subject, inhibit collagen in tissue of a subject, stimulate collagen IV in tissue of a subject, stimulate elastin in tissue of a subject, inhibit NFkB translocation in tissue of a subject, inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neurite outgrowth, promote neuron survival, and stimulate production of L1.

In one embodiment, Fragment Ab stimulates cell migration in tissue of a subject, protect tissue from cytotoxicity in tissue of a subject, inhibit apoptosis in tissue of a subject, stimulate collagen in tissue of a subject, inhibit collagen in tissue of a subject, inhibit NFkB translocation in tissue of a subject, inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neurite outgrowth, promote neuron survival, and stimulate production of L1.

In one embodiment, Fragment Ba stimulates cell migration in tissue of a subject, protect tissue from cytotoxicity in tissue of a subject, inhibit apoptosis in tissue of a subject, inhibit collagen in tissue of a subject, stimulate collagen IV in tissue of a subject, stimulate elastin in tissue of a subject, inhibit NFkB translocation in tissue of a subject, inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neurite outgrowth, promote neuron survival, and stimulate production of L1.

In one embodiment, Fragment Bb stimulates cell migration in tissue of a subject, protect tissue from cytotoxicity in tissue of a subject, inhibit apoptosis in tissue of a subject, stimulate collagen in tissue of a subject, inhibit collagen in tissue of a subject, inhibit NFkB translocation in tissue of a subject, promote neurite outgrowth, inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neuron survival, and stimulate production of D.

In one embodiment, Fragment Ca stimulates cell migration in tissue of a subject, protect tissue from cytotoxicity in tissue of a subject, inhibit apoptosis in tissue of a subject, inhibit collagen in tissue of a subject, stimulate collagen IV in tissue of a subject, stimulate elastin in tissue of a subject, inhibit NFkB translocation in tissue of a subject, promote neurite outgrowth, inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neuron survival, and stimulate production of D.

In one embodiment, Fragment Cb stimulates cell migration in tissue of a subject, protect tissue from cytotoxicity in tissue of a subject, inhibit apoptosis in tissue of a subject, stimulate collagen in tissue of a subject, inhibit collagen in tissue of a subject, inhibit NFkB translocation in tissue of a subject, inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neurite outgrowth, promote neuron survival, and stimulate production of D.

In one embodiment, Fragment Da inhibits collagen in tissue of a subject, stimulate elastin in tissue of a subject, inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neurite outgrowth, promote neuron survival, stimulate production of L1, inhibit IKBa phosphorylation, and restore impaired T-lymphocyte blastogenic response.

In one embodiment, Fragment Db inhibits collagen in tissue of a subject, stimulate elastin in tissue of a subject, inhibit tissue damage caused by ultraviolet (UV) radiation and/or protect tissue from ultraviolet (UV) radiation damage, promote neurite outgrowth, promote neuron survival, stimulate production of L1 ,and inhibit IKBa phosphorylation and restore impaired T-lymphocyte blastogenic response.

Summary of Peptide Uses

Tb4
1A
1B
2A
2B
3A
3B
4A
4B
5A
5B
6A
6B
7A
7B
Aa
Ab
Ba
Bb
Ca
Cb
Da
Db

Suppresses
P
P

P
P

U
U
U
U
U
U

inflammation

Stimulates
P

P

P
P

U
U
U
U
U
U

Migration

Protects from
P

P
P

U
U
U
U
U
U

cytotoxicity

Inhibits
P

P

U
U
U
U
U
U

apoptosis

Stimulates

P

U

U

U

collagens

Inhibits

P
P

P

P
P
P
U
U
U
U
U
U
U
U
U

collagens

Stimulates

P

P

U

U

U

collagen IV

Stimulates
P

P
P

U
U
U
U
U
U
U
U
U

Elastin

Inhibits NFkB
P

P

U

U

U

translocation

Inhibits IkBa

P

U
U

phosphorylation

Promotes
P
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U

neurite

outgrowth

Promotes
P
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U

neuron survival

Stimulates L1
P
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U

production

Inhibits tissue
P
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U

damage caused

by UV radiation

Protects tissue
P
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U
U

from UV

radiation

damage

Restores
P

U
U

impaired T-

lymphocyte

blastogenic

response

P = active

U = useful

Claims

1. A peptide having an amino acid sequence selected from Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3), Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), a variant of said Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH which has an amino acid substituent substituted for said methionine residue, an isolated R-enantiomer of Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3) or Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), an isolated S-enantiomer of Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3) or Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), or a methionine-containing variant thereof in which any methionine is oxidized or superoxidized.
2. The peptide of claim 1, having amino acid sequence Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3).
3. The peptide of claim 1, having amino acid sequence Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4).
4. The peptide of claim 1, wherein said peptide has an amino acid substituent substituted for a methionine residue, said substituent being a leucine, valine, isoleucine, alanine, phenylalanine or proline substituted for said methionine.
5. A method of at least one of suppressing inflammation in tissue of a subject in need thereof, stimulating cell migration in tissue of a subject in need thereof, protecting tissue from cytotoxicity in tissue of a subject in need thereof, inhibiting apoptosis in tissue of a subject in need thereof, stimulating collagen in tissue of a subject in need thereof, inhibiting collagen in tissue of a subject in need thereof, stimulating collagen IV in tissue of a subject in need thereof, stimulating elastin in tissue of a subject in need thereof, inhibiting NFkB translocation in tissue of a subject in need thereof, inhibiting tissue damage caused by ultraviolet (UV) radiation in need thereof, protecting tissue from ultraviolet (UV) radiation damage in need thereof, promoting neurite outgrowth in a subject in need thereof, promoting neuron survival in a subject in need thereof, stimulating production of L1 in a subject in need thereof, inhibiting IKBa phosphorylation in a subject in need thereof, or restoring impaired T-lymphocyte blastogenic response in a subject in need thereof comprising administering to said subject a peptide having an amino acid sequence selected from Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3), Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3), H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), a variant of Ac- or H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3) that has an amino acid substituent substituted for said methionine residue, an isolated R-enantiomer of Ac- or H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3) or Ac- or H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), an isolated S-enantiomer of Ac- or H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3) or Ac- or H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), a methionine-containing variant thereof in which any methionine is oxidized or superoxidized, or a combination thereof.
6. The method of claim 5, wherein said stimulating cell migration in tissue of a subject in need thereof comprises administering Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4).
7. The method of claim 5, wherein said stimulating collagen IV in tissue of a subject in need thereof comprises administering H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4).
8. The method of claim 5, wherein said stimulating elastin in tissue of a subject in need thereof comprises administering H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4).
9. The method of claim 5, wherein said inhibiting NFkB translocation in tissue of a subject in need thereof comprises administering H-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4).
10. The method of claim 5, wherein said protecting tissue from cytotoxicity in tissue of a subject in need thereof comprises administering Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3).
11. The method of claim 5, wherein said suppressing inflammation in tissue of a subject in need thereof comprises administering H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3).
12. The method of claim 5, wherein said inhibiting apoptosis in tissue of a subject in need thereof comprises administering H-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3).
13. The method of claim 5, wherein said protecting tissue from cytotoxicity in tissue of a subject comprises administering Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3).
14. The method of claim 5, wherein said promoting neurite outgrowth in a subject in need thereof comprises administering a peptide having an amino acid sequence selected from Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3), Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), or a combination thereof.
15. The method of claim 5, wherein said promoting neuron survival in a subject in need thereof comprises administering a peptide having an amino acid sequence selected from Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3), Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), or a combination thereof.
16. The method of claim 5, wherein said stimulating production of L1 in a subject in need thereof comprises administering a peptide having an amino acid sequence selected from Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3), Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), or a combination thereof.
17. The method of claim 5, wherein said inhibiting IkBa phosphorylation in a subject in need thereof comprises administering a peptide having an amino acid sequence selected from Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3), Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), or a combination thereof.
18. The method of claim 5, wherein said restoring impaired T-lymphocyte blastogenic response in a subject in need thereof comprises administering a peptide having an amino acid sequence selected from Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3), Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4), or a combination thereof.
19. A composition comprising a peptide having amino acid sequence Ac-Ser-Asp-Lys-Pro-Asp-Met-Ala-Glu-Ile-Glu-Lys-Phe-Asp-Lys-Ser-OH (SEQ ID NO: 3) and a peptide having amino acid sequence Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln-OH (SEQ ID NO: 4).
20. The composition of claim 19, wherein one or both of said peptides are isolated R-enantiomers.
21. The composition of claim 19, wherein one or both of said peptides are isolated S-enantiomers.
22. A composition comprising at least on peptide as defined in claim 1.
23. The composition of claim 22 comprising a plurality of peptides as defined therein.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 12/933,230, filed on Oct. 13, 2010, which is a 35 U.S.C. §371 National Phase Entry Application from PCT/U.S. 2009/037060, filed Mar. 13, 2009, and claims the benefit of U.S. Provisional Application Ser. No. 61/083,798, filed Jul. 25, 2008 and U.S. Provisional Application Ser. No. 61/037,207, filed Mar. 17, 2008, the contents of which are incorporated herein in their entirety by reference.

Provisional Applications (2)

	Number	Date	Country
	61037207	Mar 2008	US
	61083798	Jul 2008	US

Divisions (1)

	Number	Date	Country
Parent	12933230	Oct 2010	US
Child	13758751		US

BETA THYMOSIN FRAGMENTS

Information

Publication Number

Date Filed

Date Published

Inventors

Original Assignees

CPC

US Classifications

International Classifications

Abstract

Description

Claims

CROSS-REFERENCE TO RELATED APPLICATIONS

Provisional Applications (2)

Divisions (1)