Modification and compositions of human secretoglobin proteins

Abstract

Novel compositions of recombinant human CC10 protein have been generated by chemically modifying the pure protein in vitro. Several new synthetic preparations containing isoforms of chemically modified rhCC10 have been generated by processes that utilize reactive oxygen species and reactive nitrogen species. These preparations contain novel isoforms of rhCC10 which have been characterized with enhanced or altered biological properties compared to the unmodified protein. Preparations containing novel isoforms may be used as standards to identify and characterize naturally occurring isoforms of native CC10 protein from blood or urine and ultimately to measure new CC10-based biomarkers to assess patient disease status. These preparations may also be used to treat respiratory, autoimmune, inflammatory, and other medical conditions that are not effectively treated with the unmodified protein.

Claims

1. A process to produce synthetic CC10 protein containing a modified amino acid comprising contacting a purified CC10 molecule or a purification intermediate solution with a reactive oxygen or nitrogen species in a reaction mixture.

2. The process of claim 1 wherein the reactive oxygen or nitrogen species is hypochlorite, sodium hypochlorite, mCPBA, peroxynitrate, nitric oxide, hydrogen peroxide, oxygen, ozone, chlorine, fluorine, bromine, iodine, permanganate (MnO.sub.4), chromate (CrO.sub.4), dichromate (Cr.sub.2O.sub.7) ions, nitric acid (HNO.sub.3), perchloric acid (HClO.sub.4), and/or sulfuric acid (H.sub.2SO.sub.4).

3. The process of claim 1 wherein the temperature during contact is maintained between 0° C. and 8° C.

4. The process of claim 1 wherein the temperature during contact is maintained between 8° C. and 32° C.

5. The process of claim 1 wherein the temperature during contact is maintained between 32° C. and 45° C.

6. The process of claim 1 wherein the temperature during contact is maintained above 45° C.

7. The process of claim 1 wherein sodium (Na) and/or potassium (K) in concentration between 0.1° A and 20% on a weight to volume basis is added to the solution.

8. The process of claim 1 wherein exposure of the purified CC10 molecule or a purification intermediate to light is limited.

9. The process of claim 1 wherein an enzyme is added to the reaction.

10. The process of claim 1 wherein a buffer such as phosphate, citrate, sulfate, Tris, HEPES, or MOPS is added to the solution to maintain the pH.

11. The process of claim 1 wherein the pH of the reaction is maintained in the range of 6.5 to 7.5.

12. The process of claim 1 wherein the pH of the reaction is maintained below 6.5.

13. The process of claim 1 wherein the pH of the reaction is maintained above 7.5.

14. The process of claim 1 wherein calcium and/or magnesium is added to the solution.

15. The process of claim 1 wherein the molar ratio of purified CC10 molecule to oxidant equivalents is between 100:1 and 1:100.

16. A process to produce modified synthetic CC10 protein containing a modified amino acid comprising contacting a purified CC10 molecule or a purification intermediate with a metal ion or metal surface.

17. The process of claim 16 wherein the metal ion is nickel, iron, cobalt, copper, manganese, chromium, and/or bismuth.

18. The process of claim 16 wherein the temperature during contact is maintained between 0° C. and 8° C.

19. The process of claim 16 wherein the temperature during contact is maintained between 8° C. and 32° C.

20. The process of claim 16 wherein the temperature during contact is maintained between 32° C. and 45° C.

21. The process of claim 16 wherein the temperature during contact is maintained above 45° C.

22. The process of claim 16 wherein exposure of the purified CC10 molecule or a purification intermediate to light is limited.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0083] FIG. 1: Amino acid sequences of secretoglobins

[0084] The amino acid sequences of the monomer forms of eight human secretoglobins are shown. All sequences were taken from Genebank and signal peptides of the translation products have been removed to show the predicted N-termini of each monomer. All secretoglobins share a conserved four helical bundle secondary structure and form homodimers, heterodimers, tetramers, and large multimers.

[0085] FIG. 2: HPLC pattern of rhCC10 reacted with NaOCl

[0086] Preparations of unmodified rhCC10 (panel A) and rhCC10 reacted with increasing amounts of NaOCl oxidant equivalents (panels B-E) were analyzed by reverse phase HPLC using a C-18 column. The arrow points to the unmodified rhCC10 peak in reaction mixtures. Approximately 25 mcg of protein was loaded for each HPLC run shown. Panel A-E depict HPLC analysis of NaOCl oxidation products.

[0087] FIG. 3: SDS-PAGE of rhCC10 NaOCl reactions

[0088] A 10-20% tricine SDS-PAGE gel was used. Preparations of rhCC10 modified with increasing amounts of NaOCl; numbers of oxidant equivalents are shown for each lane. All samples, each containing ˜5 mcg protein, were reduced with 1 mM DTT in SDS loading buffer and heated to 65° C. for 15 minutes prior to gel loading.

[0089] FIG. 4: Isoelectric focusing (IEF) of rhCC10 NaOCl reactions

[0090] The IEF gel covered pH range from 3-7. Preparations of rhCC10 modified with increasing amounts of NaOCl; numbers of oxidant equivalents are shown for each lane. All samples contain ˜25 mcg protein. Samples were not reduced, exposed to SDS, or heated prior to gel loading.

[0091] FIG. 5: Western blot of IEF gel of rhCC10 NaOCl reactions using anti-rhCC10 antibody

[0092] The IEF gel covered pH range from 3-7 and was blotted to PVDF membrane, then probed with a Protein-A purified rabbit polyclonal antibody prepared using unmodified rhCC10 as the antigen. Preparations of rhCC10 modified with NaOCl reaction conditions shown in lane descriptions. All samples contain −25 mcg protein. Samples were not reduced, exposed to SDS, or heated prior to gel loading.

[0093] FIG. 6: Western blot of DNPH-treated rhCC10 NaOCl reactions using anti-DNP antibody

[0094] A 10-20% tricine SDS-PAGE gel was run on the modified rhCC10 preparations. NaOCl reaction products were run alongside MPO and mCPBA reaction products. The gel was blotted to PVDF then probed with rabbit polyclonal anti-DNP antibody (commercially available). Samples were not reduced but were mixed with SDS PAGE loading buffer and heated to 65° C. for 15 minutes prior to loading. Unmodified rhCC10 and MPO and mCPBA reaction products were not recognized by the antibody under the conditions used. Only the NaOCl reaction products contained detectable DNP, indicating the presence of carbonyl groups in these preparations.

[0095] FIG. 7: HPLC analysis of mCPBA oxidation products

[0096] Preparations of unmodified rhCC10 (FIG. 7, panel A) and rhCC10 reacted with increasing amounts of mCPBA oxidant equivalents (FIG. 7, panels B-E) were analyzed by reverse phase HPLC using a C-18 column. The arrow points to the unmodified rhCC10 peak in reaction mixtures. Approximately 25 mcg of protein in each sample was loaded for each HPLC run shown.

[0097] FIG. 8: Isoelectric focusing of rhCC10 mCPBA reactions

[0098] The IEF gel covered pH range from 3-7. Preparations of rhCC10 modified with increasing amounts of mCPBA; numbers of oxidant equivalents are shown for each lane and two different temperatures were tested. All samples contain ˜25 mcg protein. Samples were not reduced, exposed to SDS, or heated prior to gel loading.

[0099] FIG. 9: Western blot of IEF gel of rhCC10 mCPBA reactions using anti-rhCC10 antibody

[0100] The IEF gel covered pH range from 3-7 and was blotted to PVDF membrane, then probed with Protein-A purified rabbit polyclonal antibody raised against rhCC10. Preparations of rhCC10 modified with increasing amounts of mCPBA; numbers of oxidant equivalents are shown for each lane and two different temperatures were tested. All samples contain ˜25 mcg protein. Samples were not reduced, exposed to SDS, or heated prior to gel loading.

[0101] FIG. 10: Isoelectric focusing of rhCC10 mCPBA reactions; additional conditions

[0102] The IEF gel covered pH range from 3-7. Preparations of rhCC10 modified with mCPBA under additional conditions, including the presence of CaCl.sub.2) and comparison of much higher numbers of oxidant equivalents. All samples contain −25 mcg protein. Samples were not reduced, exposed to SDS, or heated prior to gel loading.

[0103] FIG. 11: Purification & mass spectral analysis of mCPBA reaction products: CC10 isoforms

[0104] C-18 RP-HPLC was used to separate each of eight individual CC10 isoforms represented as different peaks from the mCBPA reaction mixture. In this example, peak #3 (FIG. 11, panel B) was collected, rerun on the HPLC to estimate purity, then sent for mass spectral analysis (electrospray ionization method). The arrow points out the peak that was purified in this example. All samples contain ˜25 mcg protein. Results of ESI-MS analysis are shown in Panel D.

[0105] FIG. 12: Optimization of MPO-H.sub.2O.sub.2 reaction; Effect of CaCl.sub.2)

[0106] MPO-H.sub.2O.sub.2 reactions with and without 2 mM CaCl.sub.2) (respectively panels A, B, D and panels C, E) were compared using C-18 RP-HPLC to monitor reactions. All reactions were performed in the dark in citrate buffer at pH 5.0 with 50 oxidant equivalents of H.sub.2O.sub.2 at 37° C. for a total of 60 minutes. Arrows point out peaks corresponding to unmodified rhCC10. All samples contain ˜25 mcg protein.

[0107] FIG. 13 (panels A-E): HPLC analysis of MPO-H.sub.2O.sub.2 oxidation products

[0108] MPO-H.sub.2O.sub.2 reactions with 2 mM CaCl.sub.2) (panels B-E). were monitored using C-18 RP-HPLC with increasing amounts of MPO and H.sub.2O.sub.2. All reactions were performed in the dark in citrate buffer at pH 5.0 with 50 oxidant equivalents of H.sub.2O.sub.2 at 37° C. for a total of 30 minutes. Arrows point out peaks corresponding to unmodified rhCC10. All samples contain ˜25 mcg protein.

[0109] FIG. 14: Isoelectric focusing of rhCC10 MPO and H.sub.2O.sub.2 reactions

[0110] The IEF gel covered pH range from 3-7. Preparations of rhCC10 modified with increasing amounts of MPO. All reactions were performed in the dark in citrate buffer at pH 5.0 with 50 oxidant equivalents of H.sub.2O.sub.2 at 37° C. for a 1 or 24 hours. All samples contain ˜25 mcg protein. Samples were not reduced, exposed to SDS, or heated prior to gel loading.

[0111] FIG. 15: Western blot of IEF gels of rhCC10 MPO and H.sub.2O.sub.2 reactions using anti-rhCC10 antibody

[0112] The IEF gel covered pH range from 3-7 and was blotted to PVDF membrane, then probed with Protein-A purified rabbit polyclonal antibody raised against rhCC10. Preparations of rhCC10 modified with increasing amounts of MPO. All reactions were performed in the dark in citrate buffer at pH 5.0 with 50 oxidant equivalents of H.sub.2O.sub.2 at 37° C. for a 1 or 24 hours. All samples contain ˜25 mcg protein. Samples were not reduced, exposed to SDS, or heated prior to gel loading.

[0113] FIG. 16 (panels A-D): Purification and mass spectral analysis of a CC10 isoform from a MPO-H.sub.2O.sub.2 reaction

[0114] C-18 RP-HPLC was used to separate each of eight individual CC10 isoforms represented as different peaks, numbered 9-17, from the MPO-H.sub.2O.sub.2 reaction mixture (panel B). In this example, peak #10 was collected, rerun on the HPLC to estimate purity, then sent for mass spectral analysis (electrospray ionization method). The arrow points out the peak that was purified in this example. All samples contain ˜25 mcg protein. Results of ESI-MS analysis are shown in Panel D.

[0115] FIG. 17: (panels A-E) HPLC analysis of peroxynitrite oxidation products

[0116] Reactions of rhCC10 with peroxynitrite were monitored using C-18 RP-HPLC with increasing numbers of oxidant equivalents (panels B-E). Reactions were performed in water at room temperature in the dark for 1 hour. The arrow points out the peak corresponding to unmodified rhCC10. All samples contain ˜25 mcg protein.

[0117] FIG. 18 (panels A-H): Effects of pH and CaCl.sub.2) on peroxynitrite-mediated oxidation of rhCC10

[0118] Reactions of rhCC10 with peroxynitrite in the presence of CaCl.sub.2) (panels A,C,E,G) and absence of CaCl.sub.2) (panels B,D,F,H) and at different pHs were monitored using C-18 RP-HPLC with increasing numbers of oxidant equivalents. Reactions were performed using 10 oxidant equivalents at room temperature in the dark for 1 hour. Arrows point out peaks corresponding to unmodified rhCC10. All samples contain ˜25 mcg protein.

[0119] FIG. 19: Western blot analysis of peroxynitrite reaction products

[0120] A 10-20% tricine SDS-PAGE gel was run on the modified rhCC10 preparations. The gel was blotted to PVDF then probed with rabbit polyclonal anti-nitrotyrosine antibody (commercially available). Samples containing 10 mcg protein were not reduced but were mixed with SDS PAGE loading buffer and heated to 65° C. for 15 minutes prior to loading. Unmodified rhCC10 was not recognized by the antibody.

[0121] FIG. 20: Secretoglobin reaction products of ROS and RNS detected with rhCC10 protein

[0122] Schematic diagrams of oxidative modification reaction products observed with rhCC10; addition of oxygen to methionine, addition of nitro group to tyrosine, formation of carbonyl groups that are reactive with DNPH.

[0123] FIG. 21: Modification of rhCC10 by transglutaminase

[0124] Western blot of in vitro reactions of rhCC10 using TG2+4.5 mM calcium with two different biotinylated amine compounds. The reactions were performed in 25 mM Tris/150 mM NaCl pH 8.0 with 1.5 mM DTT at using 5 micro-units of TG2 enzyme at 37° C. for 60 minutes. Reactions were run on a 10-20% SDS-PAGE tricine gel, blotted to PVDF membrane, and probed with streptavidin-HRP conjugate, which recognizes the biotin. All lanes contain reducing agent to eliminate disulfide bonds.

[0125] FIGS. 22A-B: Enhanced inhibition of viral replication by modified rhCC10

[0126] Neutral red assay indicating cell survival with and without infection by two strains of influenza (H1N1: Neutral Red Assay, FIG. 22A and H5N1: Neutral Red Assay, FIG. 22B) and in the presence of 1 mg/ml unmodified and modified rhCC10.

[0127] FIGS. 23A-23C:Enhanced inhibition of neutrophil chemotaxis by modified rhCC10 ROS and RNS products

[0128] Fluorescence measurements of migrated differentiated PLB-985 cells differentiated in the presence of 100 mcg/ml of unmodified rhCC10 (CC10-A), NaOCl-modified rhCC10 (CC10-B), and mCBPA-modified rhCC10 (CC10-C).

[0129] FIG. 24A-C: Modification of CC10 by exposure to metal

[0130] FIG. 24 A: Amino acid sequences of two versions of recombinant human CC10 protein, FIG. 24 B: Overview of the purification process for T2-CC10 protein that includes IMAC. The hCC10 is in the His tagged USL fusion protein above the dotted line and is free T2 CC10 monomer and dimer below the dotted line. Abbreviations: polyethylenimine; Ni-IMAC: Nickel immobilized metal affinity chromatography: NMWCO: nominal molecular wight cutoff; UBL: ubiquitin like, and

[0131] FIG. 24 C: Far Western blot demonstrating SDC4-binding biological activity enhanced by oxidative modification achieved by processes that involve exposure to either ROS/RNS or to metal ions.

DEFINITIONS

[0132] Secretoglobin: A type of protein that includes human and non-human proteins in the CC10 family having the conserved four helical bundle motif and ranging in size from about 50-100 amino acids in length. Human secretoglobins are shown in FIG. 1.

[0133] Synthetic secretoglobin: A secretoglobin that is made by chemical or recombinant process and not isolated from a natural source.

[0134] Unmodified secretoglobin protein: A secretoglobin monomer, dimer, or other multimer that does not contain chemically or enzymatically modified amino acid residues, other than spontaneously occurring disulfide bonds between cysteine residues in homodimers and heterodimers.

[0135] Unmodified CC10 protein: A CC10 monomer, dimer, or other multimer that does not contain chemically or enzymatically modified amino acid residues, other than disulfide bonds between cysteine residues.

[0136] Modified secretoglobin: A secretoglobin monomer, dimer, or other multimer, that contains one or more chemically or enzymatically modified amino acid residues.

[0137] Modified synthetic secretoglobin: A synthetic secretoglobin monomer, dimer, or other multimer, that contains one or more chemically or enzymatically modified amino acid residues.

[0138] Modified CC10: A CC10 monomer, dimer, or other multimer, that contains one or more chemically or enzymatically modified amino acid residues.

[0139] Modified recombinant human CC10: A CC10 monomer that is made by recombinant DNA methods and contains one or more chemically or enzymatically modified amino acid residues.

[0140] Modified synthetic CC10: A CC10 monomer made by either recombinant DNA or chemical peptide synthetic methods that contains one or more chemically or enzymatically modified amino acid residues.

[0141] Modified amino acid residues: An amino acid in a protein whose side chain has been modified from the form originally present upon completion of translation of the protein.

[0142] The chemical structure of the 20 natural unmodified amino acids found in proteins can be found in any biochemistry textbook.

[0143] Carbonyl group: An aldehyde or ketone group on an amino acid side chain.

Abbreviations

[0144] CC10: Clara cell 10 kDa protein; aka CC16, CCSP, uteroglobin, urine protein-1 [0145] SCGB: Secretoglobin [0146] RNS: reactive nitrogen species [0147] ROS: reactive oxygen species [0148] MPO: myeloperoxidase enzyme [0149] iNOS: intracellular nitric oxide synthase [0150] mCPBA: meta-choloroperbenzoic acid [0151] DNP: 2, 4-dinitrophenylhydrazone [0152] DNPH: 2, 4-dinitrophenylhydrazine [0153] HNE: 4-hydroxy-2-trans-nonenal (HNE); a lipid peroxidation product [0154] MDA: malanodialdehyde

DETAILED DESCRIPTION

[0155] The modification of secretoglobins by ROS, RNS, and enzymatic activity such as MPO and TG2 has not been investigated in detail. Preliminary reports suggest that native CC10 is modified during acute inflammatory responses in vivo, such as in respiratory distress, giving rise to new isoforms thus far identified by cross-reactivity with anti-CC10 antibodies and isoelectric points different from unmodified CC10 (pI˜4.8), which is the predominant form in biological fluid samples. It has also been reported that CC10 is a substrate for tissue transglutaminase in vitro. Other than the role for Cys residues in stabilizing multimers and controlling access to the central hydrophobic cavity, there is no known physiological role for oxidation of any amino acid in any secretoglobin. We believe that reversible oxidation of Cys and Met residues is a protective physiologic mechanism by which CC10 and other secretoglobins are able to scavenge harmful ROS from the local environment, thereby sparing tissue during an inflammatory response. We further believe that the oxidation status of Cys and Met residues in secretoglobins affects the biochemical and biological properties but does not represent protein damage that results in loss of function, rather the properties and function of the oxidized secretoglobins are modulated. Likewise, oxidative and/or enzymatic modification of other secretoglobin amino acids such as tyrosine, lysine, glutamine, valine, leucine, phenylalanine, glutamate, arginine, threonine, proline, histidine, and tryptophan do not represent protein damage, but rather modulate biochemical and biological properties that enable different or enhanced activities.

[0156] The majority of known, specific ROS, RNS, and MPO-mediated amino acid modifications are associated with protein damage and loss of function. Accumulation of oxidized protein is associated with disease and aging processes (Berlett and Stadtman, 1997). However, recognition of reversible oxidation is emerging as a regulatory mechanism for modifying protein function and not just a form of damage that inactivates proteins. All eight human secretoglobins contain Cys residues that are believed to typically exist in a naturally oxidized state in which disulfide bonds between conserved cysteines at the N- and C-termini stabilize homo- and hetero-dimers, tetramers, and higher multimers. All cysteines in secretoglobins are potentially susceptible to oxidation and the formation of intra- or intermolecular disulfide bonds, particularly the respiratory secretoglobins, CC10, SCGB3A1, and SCGB3A2. The disulfide bonds between N- and C-terminal Cys in CC10 certainly stabilize the homodimer in conditions that would otherwise break apart the dimer into monomers, such as in non-reducing SDS-PAGE conditions. Similarly, the internal Cys of SCGB3A2 (Cys60 of the sequence shown in FIG. 1) stabilizes the homodimer in vitro. No particular functionality is ascribed to the dimer versus the monomer or other multimers of CC10 or SCGB3A2. However, since CC10 and SCGB3A2 both form homodimers spontaneously in vitro without any requirement for an oxidizing agent, it has not been possible to evaluate differences in biochemical properties or biological activities of forms other than the dimer. These homodimers are very stable in vitro, although there is an equilibium between monomer and dimer in any given aqueous environment and it is possible to change buffer conditions to favor a higher percentage of monomer and/or tetramer with respect to dimer. Despite that the dimer is the initial form administered to humans and animals, numerous reducible and non-reducible forms can be recovered from biological fluids (Antico, 2006). Physiologically, the in vivo glutathione redox system in the lungs likely mediates reversible oxidation of disulfide bonds in the respiratory secretoglobins and other secretoglobins that may be found in the lungs.

[0157] A physiological role for CC10 has been proposed to be the scavenging of toxic or otherwise harmful hydrophobic moieties that may be taken up and bound into the central hydrophobic cavity and thereby removed from the local tissue environment (Peter, 1992; Hard, 1995; Umland, 1992; 1994). The disulfide bonds between the Cys residues (Cys3 and Cys69) of the monomer components in each CC10 dimer are believed to act like a gate that opens and closes by reversible oxidation of the Cys residues to form and break the disulfide bonds to allow entry of a hydrophobic moiety into the central hydrophobic cavity, then trap it there. Several studies have reported the strong binding of putative in vivo CC10 ligands such as a polychlorinated biphenyls and progesterone, inside the dimer and that specific residues such as Phe6 and Tyr21 stabilize ligand binding (Callebaut, 2000).

[0158] All secretoglobins contain significant proportions of amino acids that are susceptible to oxidative and enzymatic amino acid modification. Each 70 amino acid monomer of CC10 contains a total of 42 amino acids (out of 70; >50%), listed in Table 1, that can be oxidized by physiologic processes involving ROS and RNS, leaving open the possibility of a large number of ROS and RNS reaction products, aka isoforms. TG can also be used to attach lipid or other moieties to secretoglobins via their glutamine, lysine, and cysteine residues, and not just cross-link secretoglobins to other proteins. As illustrated in the following examples, we have herein found this to be the case with rhCC10, in which oxidative and enzymatic modifications give rise to multiple isoforms that can be isolated and characterized. Preparations containing oxidatively modified rhCC10 also mediated enhanced of inhibition of viral replication and neutrophil chemotaxis, representing significant improvements on the existing unmodified CC10 drug preparation. Furthermore, the use of rhCC10 preparations modified in vitro as standards to assess CC10 isoforms contained within, or isolated from, biological samples, enables the evaluation of native CC10 isoforms as biomarkers of pulmonary status in chronic diseases and acute conditions. Thus, in the absence of oxidative or enzymatic amino acid modification, a secretoglobin may have no effect on a particular cell type, but has a different effect after modification because the modification enabled or disabled binding to a cell surface receptor, cell signaling molecule, lipid, ligand, structural protein, or other intra- or extracellular component. The effects of oxidative and/or enzymatic amino acid modification on the biochemical and biological properties of secretoglobins, therefore, opens up new possibilities for the use of modified secretoglobins in mediating pharmacological effects not previously possible using unmodified preparations, as well as for use as standards to evaluate novel isoforms of native secretoglobins as biomarkers of disease status in various patients, including, but not limited to patients with cancer, respiratory diseases, autoimmune diseases, acute or chronic infections, allergies, metabolic diseases, cardiovascular diseases, hematologic disorders, and exposures to smoke, chemical pollutants, toxins or other insult.

EXAMPLES

Example 1: Chemical Modification of rhCC10 by ROS: Sodium Hypochlorite (NaOCl)

[0159] Each reaction was initiated at ˜4° C. (on ice) by adding NaOCl (9.2 □L; 0.05% solution in water, 62.1 nmol, 5 equivalents) to a solution of the protein (0.2 mg, 12.42 nmol) in 10 mM phosphate buffer, pH 7.4 or plain water, mixing briefly and incubating on ice for 15 minutes in the dark (total volume of 0.2 mL). The reaction was quenched by adding L-methionine (9.3 □L; 10 mM in water, 93.15 nmol), then incubated for 20 min and warmed to room temperature.

[0160] Several reactions were performed using equivalents of the oxidant (“oxidant equivalents”) ranging from 1-100 FIG. 2, panels B-E. Oxidation of rhCC10 was monitored using HPLC, in which new modified isoforms appeared as new HPLC peaks, eluting earlier than unmodified rhCC10, as shown in FIG. 2. Reactions were concentrated by Speedvac and then resuspended in water. Approximately 25 □g of each sample was injected onto the HPLC column (VYDAC Polymeric C18 column 300A 5□m, 2.1 mm×250 mm, Cat #218TP52) on an Agilent 1100 system using a mobile phase as follows: A: water; B: 95% acetonitrile+5% water (both containing 0.1% TFA) at a flow rate of 0.3 mL/min. Output was monitored by UV absorption at 214 nm.

[0161] Increasing the number of oxidant equivalents of NaOCl increased the number of rhCC10 isoforms as well as the peak heights, indicating increased amounts of each isoform as the reaction progressed. At 20 oxidant equivalents, the HPLC shows that essentially all of the unmodified rhCC10 is gone and only modified isoforms remain. SDS-PAGE of these preparations under reducing conditions showed monomeric protein (6 kDa) as expected, but also showed dimer (˜12 kDa), tetramer (˜24 kDa), hexamer (˜32 kDa), and higher multimer bands remaining, as shown in FIG. 3. This is the first report of a tetramer formed by CC10 and stable to reducing SDS-PAGE conditions in the absence of transglutaminase activity. The presence and predominance of the monomer indicates that the amino acid sequence for rhCC10 is largely intact. Even at 100 oxidant equivalents, there are faint CC10 monomer, dimer, tetramer, and higher multimer bands on SDS-PAGE, although the majority of protein is missing and appears to be destroyed with that many oxidation equivalents.

[0162] Interactions of the modified and unmodified rhCC10 with the C-18 column reflect hydrophobic interactions between the protein and chromatography resin. The modified isoforms elute faster than the unmodified rhCC10, indicating that the amino acid residues on the surface of the modified protein are less hydrophobic than the unmodified protein. Changes in the surface hydrophobicity pattern likely correspond with changes in surface charge, which can be measured by the isoelectric point. Samples were analyzed by isoelectric focusing using pH 3-7 isoelectric focusing gels as shown in FIG. 4. There is a progressive shift in pI towards more acidic isoforms less than 4.5. There is also a band at pI˜5.5 in the reactions with 2 and 5 equivalents that disappears at 20 equivalents and may represent a reaction intermediate. Analysis of these reactions by Western blot of the IEF gel shows that all acidic NaOCl isoforms <4.5 are recognized by a rabbit polyclonal anti-rhCC10 antibody as shown in FIG. 5, however, the tetramer is not recognized by the polyclonal anti-rhCC10 antibody.

[0163] The extent of the chemical reaction and modification of rhCC10 can be estimated by the detection of reactive carbonyl groups. The presence of carbonyl groups in ROS-reacted rhCC10 samples can be detected by labeling the carbonyl groups with 2,4-dinitrophenylhydrazine (DNPH), which adds a dinitrophenylhydrazone group (DNP), then analyzing the reaction products by Western blot using anti-DNP antibody as shown in FIG. 6. There is a baseline signal for monomer and tetramer in the unmodified CC10 (lane 8), which is exceeded in all other samples, regardless of type of ROS used in the reaction. Therefore, all ROS reactions produced some species that contained carbonyl groups. The unmodified dimer, and dimer in MPO and mCPBA modified preps show no reactivity and even blocked the background (see “ghost bands” at dimer position in lanes 2, 3, and 8.) There appears to be a combination effect of rhCC10 concentration and buffer in the NaOCl reaction. The signal strength in lane 4 is over 10× greater than lane 5, which is more than expected by the 2× difference in protein present. This suggests that higher rhCC10 concentration provides for a more extensive reaction than lower concentration when the reaction is done in water. The signal strength in lanes 4 and 7 is equal, despite that lane 7 contains half the protein, indicating that the reaction is more efficient in 10 mM phosphate buffer, pH 7.4 than in water. The signal strength in lane 6 is much less than in lane 7, despite that the same amount of protein is present. These observations indicate that the NaOCl reaction was more efficient when rhCC10 concentration is lower in the presence of buffer. Therefore, effect of rhCC10 concentration on reaction efficiency is opposite in water versus buffer. These differences illustrate how the process for chemical modification of rhCC10 with NaOCl is optimized. For example, an optimized process for NaOCl-mediated chemical modification of CC10 would involve the use of a lower concentration of rhCC10, in the presence of a low strength phosphate buffer at neutral pH.

Example 2: Chemical Modification of rhCC10 by ROS: mCPBA

[0164] Each reaction was initiated at ˜24° C. (room temperature) by adding meta-choloroperbenzoic acid (mCPBA) (6.21 □L, 2 mM in water, 12.42 nmol, 2 equivalents) in 1 portion to a solution of the protein (0.1 mg, 6.21 nmol) in water at 24° C. and incubating for 15 minutes in the dark with occasional stirring (total volume of 0.2 mL). The reaction was stopped by the addition of L-methionine (1.8 □L; 10 mM in water, 18.6 nmol) and incubated for 20 min at 24° C. Several reactions were performed using oxidant equivalents of mCPBA ranging from 2-100.

[0165] Oxidation of rhCC10 was monitored using HPLC. Reactions were concentrated in a Speedvac and then resuspended in water. Approximately 25 □g of each sample was injected onto the HPLC, as with the NaOCl reactions. New modified isoforms appeared as new HPLC peaks, eluting earlier than unmodified rhCC10, as shown in FIG. 7. Isoelectric focusing of the mCPBA reactions, shown in FIG. 8, revealed that multiple new isoforms were generated, including a cluster of new isoforms in the pI 4.5-5.2 range (4.6, 4.7, 4.9, 5.1, 5.2), two isoforms above 5.3 (˜5.5, ˜5.8) and one isoform below 4.5 (˜4.3). These additional 8 bands differed from the original unmodified rhCC10 with a major band at pI 4.8 and a minor band at ˜4.65. An important parameter in optimization of the reaction is temperature. The temperature of the reaction, 4° C. vs 21° C., did not affect the products or the apparent proportions of each product. Western blot of the IEF gel, shown in FIG. 9, demonstrated that the majority of these isoforms are recognized by a rabbit polyclonal antibody raised against rhCC10. However, like the tetramer form generated by the NaOCl reaction, the band at pI 4.3 was not recognized by the anti-rhCC10 antibody, suggesting that the structure of the protein was dramatically changed when 10 eq mCPBA were used. The isoforms below the main immunoreactive band at 4.8, also showed less signal than would be expected based on the intensity of staining in the IEF gel. Further analysis of reaction conditions showed that the presence of CaCl.sub.2) could prevent modification of rhCC10 by mCPBA (FIG. 10, lane 2), that 100 eq mCPBA completely eliminates all of the original unmodified protein leaving only more acidic isoforms (pIs 4.0, 4.3, 4.5; lane 4), and that rhCC10 is destroyed if the reaction is run too long (lane 3).

[0166] In order to further characterize the CC10 isoforms generated in the mCPBA reaction, a protein sample of each of 8 separate major HPLC peaks (numbered 1-8) was collected, concentrated using a Speedvac, and verified by repeat HPLC to represent a single peak; for example peak 3, as shown in FIG. 11. The samples were then analyzed by electrospray mass spectrometry (ESI-MS) to obtain molecular weights for each isoform. Table 2 shows the results of the MS analysis of isoforms contained in individual HPLC peaks. All CC10 isoforms had a greater molecular weight (MW) than the unmodified form, which has a MW of 16,110 daltons (Da). The addition of an oxygen adds 16 Da. The mCPBA reaction oxidized methionine residues before modifying other amino acids. This is clear since the average mass of 5 of the 8 peaks was increased by a multiple of 16 (eg. peaks 2, 4, 5, 6, and 8). Peak 3 did not increase by an even multiple of 16; this peak contains dimers in which the average number of oxygens is 5.25 or may represent more complex modification than simple addition of oxygen. Peaks 1 and 7 did not yield usable mass spectra.

TABLE-US-00002 TABLE 2 Mass spectral analysis of isolated mCPBA CC10 isoforms # of Mass Mass change Oxygens Peak # (daltons) (daltons) added 1 Not obtained 2 16206.5 +~96 6 3 16194   +~84 5.25 4 16190.7 +~80 5 5 16174.1 +~64 4 6 16173.5 +~64 4 7 Not obtained 8 16125.1 +~16 1

Example 3: Chemical Modification of rhCC10 by ROS: Myeloperoxidase Enzyme (MPO) and Hydrogen Peroxide (H.SUB.2.O.SUB.2.)

[0167] Modification of rhCC10 by MPO plus H.sub.2O.sub.2 was monitored using HPLC. The reaction of rhCC10 with MPO-H.sub.2O.sub.2 required extensive optimization before any CC10 modifications were observed. Initial reactions performed in phosphate buffered saline (PBS), pH 7.4, in the absence of calcium chloride (CaCl.sub.2)) were unsuccessful. Very modest increases in the number and height of new HPLC peaks were achieved in phosphate buffer at neutral pH with increasing amounts of MPO and H.sub.2O.sub.2. However, the lowering of pH to 5 using citrate buffer and the addition of CaCl.sub.2) dramatically increased the CC10 reaction products detectable as new HPLC peaks as shown in FIG. 12. Once calcium was added and pH was optimized, the amounts of MPO and H.sub.2O.sub.2 oxidant equivalents were re-optimized and a reproducible HPLC peak pattern showing a clear MPO- and H.sub.2O.sub.2-concentration and time dependent peak progression was observed. Briefly, a solution of the protein (0.1 mg, 6.21 nmol) in 2 mM CaCl.sub.2) and 10 mM citrate buffer (pH 5) was incubated at 37° C. for 30 min. The reaction was initiated at 37° C. by adding MPO (2.5 □L, 10 □g/mL in water, 25 ng) and H.sub.2O.sub.2 (1.55 □L, 100 mM in water, 155.25 nmol, 25 equivalents) and incubated in the dark for 30 min at 37° C. with occasional stirring. Another aliquot of MPO (25 ng) and H.sub.2O.sub.2 (1.55 □L) solutions were added and incubated for further 30 min at that temperature with stirring (total volume of 0.2 mL). The reaction was stopped by the addition of L-methionine (4.66 □L; 0.1 M in water, 0.466 □mol) and incubated for 30 min at 37° C. Reactions were typically concentrated in a Speedvac, then resuspended in water, and about 25 □g of each sample was injected onto the HPLC, as with the NaOCl and mCPBA reactions. Modified isoforms appeared as new HPLC peaks, eluting earlier than unmodified rhCC10, as shown in FIG. 13.

[0168] Isoelectric focusing of the MPO and H.sub.2O.sub.2 reactions, shown in FIG. 14, revealed that only 2 isoforms with altered isoelectric points were generated, including an isoform at 5.5 and one or more isoforms below 4.7. Unmodified CC10 sometimes appears as a major band at 4.8 plus a minor band at 4.7 in IEF gels (likely dimer and monomer, respectively). The gel was loaded with 25 mcg of each preparation, so that minor bands would not be missed. Therefore, the multiple peaks observed by HPLC (n=8) do not match the number of new bands on IEF (n>2). This indicates that, remarkably, at least 6 of the isoforms separated by HPLC on the basis of hydrophobic interactions retain the same surface charge as unmodified CC10. Western blot of an identical IEF gel, shown in FIG. 15, demonstrated that these pI 4.8 isoforms are recognized by a rabbit polyclonal antibody raised against unmodified rhCC10.

[0169] In order to further characterize the CC10 isoforms generated in the MPO-H.sub.2O.sub.2 reactions, a protein sample of each of 8 major separable HPLC peaks (numbered 9-17) was collected, concentrated using a Speedvac, and verified by repeat HPLC to represent a single peak; for example peak 10, as shown in FIG. 16. The samples were then analyzed by electrospray mass spectrometry (ESI-MS) to obtain molecular weights for each isoform. Table 3 shows the results of the MS analysis. All CC10 isoforms had a greater molecular weight (MW) than the unmodified form, which has a MW of 16,110 daltons (Da). In contrast to the mCPBA isoforms, none of the MPO-H.sub.2O.sub.2 isoforms showed molecular weight increases that were multiples of 16 (eg. simple additions of oxygen). Modifications under the conditions tested may include some combination of the addition of oxygen, chlorine, or other adducts, as well as the formation of carbonyl groups.

TABLE-US-00003 TABLE 3 Mass spectral analysis of isolated MPO-H.sub.2O.sub.2 CC10 isoforms # of Mass Mass change Oxygens Peak # (daltons) (daltons) added 9 Not obtained 10 16234.7 124.7 7.79 11 16211.6 101.6 6.35 12 16218.9 108.9 6.81 13 16194.3 84.3 5.27 14 16191.7 81.7 5.11 15 16171.1 61.1 3.82 16 16188.1 78.1 4.88 17 16177   67 4.19

Example 4: Chemical Modification of rhCC10 by RNS: Peroxynitrite

[0170] Modification of rhCC10 by peroxynitrite was monitored using HPLC. Each reaction was initiated at ˜23° C. (room temperature) by adding commercially available peroxynitrite reagent (10-100 equivalents) to 0.1 mg of protein (total reaction volume 0.2 mL), stirring briefly and incubating for 1h in the dark. Reactions were typically concentrated in a Speedvac, then resuspended in water, and about 25 □g of each sample was injected onto the HPLC, as with the other reactions. Modified isoforms appeared as new HPLC peaks, eluting both earlier and later than unmodified rhCC10, as shown in FIG. 17, panels A-B. Four new major peaks are evident using 10 equivalents, in addition to a peak that elutes at the same retention time as unmodified CC10. Use of over 20 equivalents resulted in loss of peaks, which broaden into a long bump centered at a point that elutes slightly sooner than unmodified CC10 (FIG. 17, panels D-E). This broad bump pattern indicates that a vast number of modifications and isoforms are generated. Given the loss of resolution of HPLC peaks, 10 equivalents was the maximum used in further experiments. Further optimization was performed at pH ranging from 3-6 (10 mM citrate buffer), with and without 2 mM CaCl.sub.2) as shown in FIG. 18, panels A-H. In contrast to MPO-H.sub.2O.sub.2 and mCPBA, where calcium and pH had a significant effect on the reactions, there was no apparent impact on the peroxynitrite reaction products.

[0171] Each human CC10 monomer contains a single tyrosine, which these results show is susceptible to nitration in the presence of RNS without the need to denature the protein with 8M urea, or elevate the reaction pH to 8.5-9.0, as previously observed using native rabbit uteroglobin and tetranitromethane instead of RNS (peroxynitrite) (Saavedra, 1980). As the reaction with peroxynitrite progresses, intermolecular bonds may form di-tyrosine complexes in different monomers. The isoforms generated by the peroxynitrite reactions were largely intact human CC10 homodimer with larger covalently linked complexes as shown by Western blot of SDS-PAGE in FIG. 19. Peroxynitrite reactions with human CC10 were run under non-reducing conditions in a 1-10% SDS-PAGE tricine gel, which was blotted to PVDF membrane, blocked with 4% non-fat milk, and probed with rabbit polyclonal anti-nitrotyrosine antibody. The blot shows immunoreactive human CC10 dimers, tetramers, and “smears” of higher molecular weight complexes, proving that the tyrosine residue in the human CC10 monomer and/or dimer is accessible from the surrounding environment and susceptible to modification without denaturation. Nitration of tyrosine does not disrupt dimer or tetramer stability. This pattern further indicates that tyrosine nitration favors the formation of large complexes, likely linked together by both di-tyrosines and disulfide bonds, but does not generate the distinct sets of thermodynamically favored multimers achieved by simple disulfide bond rearrangements in the absence of di-tyrosine formation.

[0172] The results herein (Examples 1-4) demonstrate that multiple reactive oxygen or nitrogen species may be used in the process to produce a ROS- or RNS-modified secretoglobin, such reactive oxygen or nitrogen species including but not limited to hypochlorite, sodium hypochlorite, mCPBA, peroxynitrite, nitric oxide, hydrogen peroxide, oxygen, ozone, chlorine, fluorine, bromine, iodine, permanganate (MnO4), chromate (CrO4), dichromate (Cr2O7) ions, nitric acid (HNO3), perchloric acid (HClO4), and/or sulfuric acid (H2SO4). The results demonstrate that the concentration of sodium (Na) used in the process to produce a ROS- or RNS-modified secretoglobin is about 0.9% on a weight to volume basis, but may range between 0.1% and 20%. Potassium (K) alone or in combination with sodium, may also be used at a concentration of 0.1%-20%. The process may also utilize a buffer such as phosphate, citrate, sulfate, Tris, HEPES, or MOPS in order to maintain the pH at a constant level between pH 3.0 and 9.0, but most optimally in the 6.5-7.5 range. Calcium and/or magnesium may also be used in the process to manipulate the secretoglobin conformation to produce specific isoforms.

[0173] The results herein further demonstrate that the preferred temperature of the process for ROS and RNS modification of a secretoglobin is close to 0° C., in the range of 0−8° C., and that the most useful range of molar ratios of CC10 molecules to oxidant equivalents ranges between 1:1 and 1:50. However, as the temperature is increased, the molar ratio of oxidant equivalents may be decreased and one would expect that changes in secretoglobin conformation at below normal body temperature (<32° C.), body temperature and fever range (>32-45° C.), and over physiologic temperatures (>45° C.) would impact process efficiency and the isoforms produced.

Example 5: Modification of CC10 by Transglutaminase

[0174] CC10 was shown to be an in vitro substrate of tissue transglutaminase (aka TG2) (Manjunath, 1984), and is cross-linked to itself and other proteins via glutamine and lysine residues. Determination of availability of glutamine in uteroglobin as an acyl donor/amine acceptor was performed using biotin linked to two different monoamine groups. Purified guinea pig liver transglutaminase and monoamine-biotin reagents; 5-(Biotinamido)pentylamine and (+)-Biotinyl-3,6-dioxaoctanediamine; were purchased from a commercial vendor. The reactions were performed in 25 mM Tris/150 mM NaCl pH 8.0 with 1.5 mM DTT. Where applicable, CaCl.sub.2) was used at a final concentration of 4.5 mM. Calcium is a TG cofactor required for the crosslinking of glutamine and lysine residues. In the absence of calcium and reducing agent, TG2 mediates a rearrangement of disulfide bonds in CC10, resulting in formation of a “ladder” of multimers that can be reduced with a reducing agent (not shown). The protein and amine of interest were combined in buffer with or without calcium to an assay volume of 0.1 mL. Samples were pre-incubated at 37° C. for 30 minutes prior to the addition of the transglutaminase. EDTA at a final concentration of 50 mM was added to the samples without calcium and acted as negative controls. After the pre-incubation 5 □U of transglutaminase was added to each tube and the reaction was allowed to proceed at 37° C. for 60 minutes. After 60 minutes EDTA (50 mM) was added to the tubes containing calcium to stop the reaction. One hundred □L of SDS sample buffer plus reducing agent (1 mM DTT) was added to each reaction, which were then heated at 95° C. for 10 minutes prior to separation on a SDS-PAGE gel. The gel was blotted to a PVDF membrane. Blocking was done for 1 hour at room temperature using 5% BSA (filtered through a 2 micron membrane). Washes between incubations were done with PBS-Tween (0.4%). Biotin groups were detected on the labeled protein(s) by incubating with a streptavidin-alkaline phosphatase conjugate. Visualization was performed with colorimetric reagents (NBT/BCIP) as shown in FIG. 21. The results show that glutamines and lysines in CC10 are both acyl donors and acyl acceptors for TG2 reactions. The reaction is calcium dependent and is abolished by the removal of calcium with a chelating agent. The non-reducible high molecular weight bands indicate that CC10 contains at least two reactive glutamine—lysine pairs, since the high molecular weight bands represent cross-linked CC10 with at least one glutamine-amine biotin amine per complex (such that a single monomer is both labeled with the biotin tag and cross-linked to at least one other monomer). This also illustrates that moieties such as labels, chemicals, lipids, and peptides containing primary amine groups may be added to rhCC10 using TG2 in the presence of calcium and a reducing agent while other moieties containing sulfhydryl groups may be added to rhCC10 using TG in the absence of a reducing agent.

Example 6: Enhanced Inhibition of Influenza Replication In Vitro by Modified rhCC10 Compared to Unmodified rhCC10

[0175] In order to determine the effect of modification on the activity of rhCC10, a single pool of modified rhCC10 was made by combining equal aliquots of rhCC10 reactions with NaOCl, mCPBA, MPO+H.sub.2O.sub.2, and peroxynitrite. All HPLC peaks from each reaction were represented in the pool. Modified and unmodified rhCC10 preparations were diluted in eight half-log dilutions in MEM solution at the highest concentrations possible with the sample available. Each dilution was added to 5 wells of a 96-well plate with 80-100% confluent MDCK cells. Three wells of each dilution were infected with virus (H1H1 or H5N1), and two wells remained uninfected as toxicity controls. The multiplicity of infection (MOI) for each virus was between 0.1-1.0. Media was MEM solution with 10 units/mL trypsin. After untreated virus control wells reached maximum cytopathic effect (CPE), plates were then stained with neutral red dye for approximately 2 hours, then supernatant dye was removed from the wells and the incorporated dye was extracted in 50:50 Sorensen citrate buffer/ethanol, then the optical density at 540 nm was read on a spectrophotometer. Neutral red dye is taken up in live cells and used as a measure of cells remaining after viral infection. Results are shown in FIGS. 22A-B FIG. 22. Surprisingly, the modified rhCC10 preparation demonstrated enhanced anti-viral activity against two strains of influenza rather than a loss of function that is normally the consequence of oxidative protein modification.

Example 7: Enhanced Inhibition of Neutrophil Chemotaxis In Vitro by Modified rhCC10 Compared to Unmodified rhCC10

[0176] Human PLB-985 cells are an immature myeloid leukemia cell line that can be differentiated in vitro essentially into mature human neutrophils (Pedruzzi, 2002). The differentiated PLB-985 cells can then be used as surrogates for actual human neutrophils isolated from peripheral blood in neutrophil function assays such as chemotaxis in response to a variety of stimuli, including fMLP. fMLP is a formylated peptide (Met, Leu, Pro) that is produced only by bacteria and is a signal of bacterial overgrowth to the body that elicits a potent anti-inflammatory response, including migration of neutrophils along a concentration gradient towards the source of the fMLP. Both unmodified and modified rhCC10 were evaluated as inhibitors of differentiated PLB-985 (dPLB-985) in this model.

[0177] Cells were grown in RPMI 1640 medium containing 10% FBS, 100 U/ml penicillin, and 100 μg/ml streptomycin at 37° C. in a humidified atmosphere of 5% CO2. To induce a differentiation to the mature neutrophil phenotype, PLB-985 cells were cultured in medium supplemented with 300 μM dibutyril cyclic AMP for 3 days before each experiment. Differentiated PLB-985 cells were resuspended in RPMI-1640 (without phenol red) containing 10% FBS (RPMI/FBS) at 10.sup.7 cells/ml. The cells were pre-incubated with 5 μg/ml calcein-acetoxymethyl ester at 37° C. for 30 min in the dark with constant agitation. The cells were then washed and resuspended in RPMI/FBS at 2×10.sup.6 cells/ml. The dPLB-985 cells were incubated with 100 mcg/ml rhCC10 preparations at 37° C. for 60 min or PBS (50%). Cell migration was monitored using a 96-well ChemoTX disposable chemotaxis system (Neuro Probe). The wells of the lower chamber of the plate were filled with 32 μl of fMLP at 10.sup.−8 M. The polycarbonate filters (3 μM) were positioned on the plate, and dPLB-985 cells (30 μl; 60,000 cells/well) were placed on the filter and allowed to migrate for 120 min at 37° C. in the presence of 5% CO2 in the dark. The cells that had not migrated were removed by gently wiping the filters with a tissue.

[0178] The fluorescence of the cells in the filters was measured with a microplate fluorescence reader using excitation and emission wavelengths of 485 and 530 nm, respectively. The fluorescence from known numbers of dPLB-985 were obtained by placing them into the bottom chamber and a standard curve was generated (FIG. 23, B). FIG. 23C shows that unmodified rhCC10 (CC10-A) slightly inhibits neutrophil migration in response to fMLP, while NaOCl-modified rhCC10 (CC10-B) and mCPBA-modified rhCC10 (CC10-C) both inhibit neutrophil migration to a significantly greater extent. It was surprising to discover that these reactions enhanced rhCC10 activity rather than causing the more typical loss of function that is more often the result of oxidative modification.

Example 8: Modification of CC10 by Exposure to Metal

[0179] Recombinant human CC10 was produced using a ubiquitin-like (UBL) fusion protein expression system in E. coli bacteria, as described in Examples 2 and 3 of U.S. Pat. No. 9,765,127, except that the human CC10 sequence according to FIG. 24 A was produced instead of the human SCGB3A2 sequence. The version of rhCC10 produced using the UBL system will be referred to as “T2-CC10” and the original preparation of rhCC10 described in U.S. Pat. No. 7,122,344 is referred to as rhCC10. This UBL expression system has the advantage that extra N-terminal amino acids are not required for robust E. coli expression, and T2-CC10 lacks the two N-terminal alanine (AA) residues (FIG. 24 A). It uses a N-terminal histidine purification tag on an UBL fusion partner and with the hCC10 at the C-terminus of the UBL component. The purification scheme for T2-CC10 is shown in FIG. 24 B. The his tag enables the fusion protein to be purified from the crude lysate and other purification intermediates using immobilized metal affinity chromatography (IMAC). IMAC uses a chromatographic resin (usually sepharose) that is loaded with metal ions such as nickel, cobalt, copper, iron, manganese, chromium, and/or bismuth, or other metals. The CC10 component in the purification intermediate is juxtaposed to nickel metal ions during the purification step in which the his tagged UBL fusion protein binds to the IMAC resin. Metal ions and metal surfaces can function as oxidizing agents, similar to ROS, under certain conditions, such as those used during the IMAC purification step. All purification steps are typically carried out in ambient light at room temperature or between 2-8° C. and purification intermediates are typically stored at 2-8° C. between steps. However, variations in temperature may be used to manipulate the efficiency of different purification steps and/or the efficiency of CC10 modification. Therefore, T2-CC10 produced using this process is modified in a manner similar to that when purified rhCC10 made according to U.S. Pat. No. 9,765,127 is exposed to ROS and RNS in vitro.

[0180] One of the functional consequences of ROS modification of human CC10 is that binding of Syndecan-4 (SDC4) is enhanced as described in Examples 3, 8, and 9 of U.S. patent application 62/925,058. FIG. 24 C shows a Far-Western blot illustrating that unmodified rhCC10 binds poorly to immobilized SDC4, whereas ROS-modified and RNS-modified rhCC10 and T2-CC10 bind well to immobilized SDC4. The Far-Western blot method was done according to Example 3 of U.S. patent application 62/925,058. Briefly, 200 ng each of SDC1, SDC4, GPC3, rhCC10 (aka rhSCGB1A1) (positive control), and bovine serum albumin (BSA) (negative control), all in PBS pH 7.4, were spotted onto nitrocellulose membranes and allowed to dry. The membranes were blocked in 5% non-fat dry milk in PBS pH 7.4 for 1 hour at room temperature. After blocking, the membranes were equilibrated in citrate buffer, pH 6.5, then the unmodified rhCC10, ROS-modified rhCC10, RNS-modified rhCC10, or T2-CC10 was diluted in citrate buffer, pH 6.5, to 50 mcg/ml, added to the blocked membrane, and incubated overnight at 4° C. with gentle agitation. The membrane was washed with PBS pH 7.4, 0.1% Tween-20 (PBS-T) and incubated for 1 hour at room temperature with gentle agitation in the primary anti-human CC10 antibody, which was diluted 1:1,000 in 0.1% non-fat dried milk in PBS-T. The membranes were washed with PBS-T and incubated in secondary antibody, which were each conjugated to alkaline phosphatase enzyme, diluted 1:8,000 in 0.1% non-fat dried milk in PBS-T, and incubated with the membranes for 1 hour at room temperature. The membranes were washed with PBS-T then incubated in NBT/BCIP to develop color.

[0181] The data illustrate that the ROS-modified rhCC10, RNS-modified rhCC10, and T2-CC10 are essentially equivalent in binding to SDC4, while the unmodified rhCC10 binding to SDC4 is significantly lower. Since the T2-CC10 was not ROS or RNS modified after it was purified and no other steps in the purification allow either the fusion protein or the T2-CC10 to come into contact with any type of oxidizing agent, we infer that the oxidative modification took place during the exposure of the UBL-T2-CC10 fusion protein to metal ions. This observation has significant implications not only in that it is possible to produce a version of recombinant human CC10 that has the enhanced potency properties of ROS-modified or RNS-modified rhCC10 without having to perform the extra step of exposing the purified protein to ROS or RNS, but also that exposure to metal ions and/or surfaces, such as injection needles or other metal delivery device components, could positively or negatively impact the biological activities of the purified recombinant human CC10 protein.