TY - JOUR
T1 - Immunological characterisation of barley polypeptides in lager foam
AU - Kauffman, Juliet A.
AU - Mills, E. N.Clare
AU - Brett, Gary M.
AU - Fido, Roger J.
AU - Tatham, Arthur S.
AU - Shewry, Peter R.
AU - Onishi, Akiko
AU - Proudlove, Michael O.
AU - Morgan, Michael R.A.
PY - 1994/11
Y1 - 1994/11
N2 - Eight monoclonal antibodies (mAb) recognising barley polypeptides have been identified from a library developed to wheat prolamins. The specificity or the mAb has been determined using enzyme‐linked immunosorbent assay (ELISA) and immunoblotting. Six were of broad specificity, recognising D, B, C and γ‐hordeins to varying degrees by both techniques. IFRN 0610 preferentially recognised γ‐hordeins by ELISA but was highly specific for this hordein group by immunoblotting. Another mAb, IFRN 0624, bound to a Mr ∽ 18000 polypeptide belonging to the CM protein (trypsin/α‐amylase inhibitor) family by immunoblotting. This, or a related protein, was detected by 0624 in all hordein fractions using ELISA. These mAb, together with two others described previously and found to recognise the repeat motif of C hordein, were used in ELISA and immunoblot analysis of Octyl‐Sepharose fractions of lager foam. Hordein polypeptides were found in all foam fractions, indicating that much foam protein originates from the malt. The CM‐like protein was found present in a virtually unmodified form. In contrast, the repeat motif of C hordein was not detected, indicating that it had either been destroyed or masked by other beer constituents. The foam stabilising agent, propylene glycol alginate (PGA), increased the apparent hydrophobicity of hordein fragments suggesting that at least part of the activity of PGA is mediated by interactions with the hordein components of foam.
AB - Eight monoclonal antibodies (mAb) recognising barley polypeptides have been identified from a library developed to wheat prolamins. The specificity or the mAb has been determined using enzyme‐linked immunosorbent assay (ELISA) and immunoblotting. Six were of broad specificity, recognising D, B, C and γ‐hordeins to varying degrees by both techniques. IFRN 0610 preferentially recognised γ‐hordeins by ELISA but was highly specific for this hordein group by immunoblotting. Another mAb, IFRN 0624, bound to a Mr ∽ 18000 polypeptide belonging to the CM protein (trypsin/α‐amylase inhibitor) family by immunoblotting. This, or a related protein, was detected by 0624 in all hordein fractions using ELISA. These mAb, together with two others described previously and found to recognise the repeat motif of C hordein, were used in ELISA and immunoblot analysis of Octyl‐Sepharose fractions of lager foam. Hordein polypeptides were found in all foam fractions, indicating that much foam protein originates from the malt. The CM‐like protein was found present in a virtually unmodified form. In contrast, the repeat motif of C hordein was not detected, indicating that it had either been destroyed or masked by other beer constituents. The foam stabilising agent, propylene glycol alginate (PGA), increased the apparent hydrophobicity of hordein fragments suggesting that at least part of the activity of PGA is mediated by interactions with the hordein components of foam.
KW - Hordeins
KW - beer foam
KW - hydrophobicity
KW - monoclonal antibodies
UR - http://www.scopus.com/inward/record.url?scp=84988148563&partnerID=8YFLogxK
U2 - 10.1002/jsfa.2740660312
DO - 10.1002/jsfa.2740660312
M3 - Article
AN - SCOPUS:84988148563
SN - 0022-5142
VL - 66
SP - 345
EP - 355
JO - Journal of the Science of Food and Agriculture
JF - Journal of the Science of Food and Agriculture
IS - 3
ER -