A NEWLY IDENTIFIED 105-KD LOWER LAMINA-LUCIDA AUTOANTIGEN IS AN ACIDIC PROTEIN DISTINCT FROM THE 105-KD GAMMA-2 CHAIN OF LAMININ-5

Citation
Ls. Chan et al., A NEWLY IDENTIFIED 105-KD LOWER LAMINA-LUCIDA AUTOANTIGEN IS AN ACIDIC PROTEIN DISTINCT FROM THE 105-KD GAMMA-2 CHAIN OF LAMININ-5, Journal of investigative dermatology, 105(1), 1995, pp. 75-79
Citations number
18
Categorie Soggetti
Dermatology & Venereal Diseases
ISSN journal
0022202X
Volume
105
Issue
1
Year of publication
1995
Pages
75 - 79
Database
ISI
SICI code
0022-202X(1995)105:1<75:ANI1LL>2.0.ZU;2-L
Abstract
A 105-kD lower lamina lucida antigen (p105) has been detected by autoa ntibodies (anti-p105) from patients with a novel immunobullous disease , To distinguish p105 from other known lamina lucida components, we pe rformed comparative immunoblotting on purified human amniotic laminin- 5 (kalinin), 804G matrix (enriched in laminin-5), and keratinocyte and fibroblast proteins using anti-804G matrix antibody (J-18) and anti-p 105, J-18 labeled the truncated laminin-5 gamma 2 chain in amniotic la minin-5, 8046 matrix, and keratinocyte conditioned medium, but did not label fibroblast cytosol, Conversely, anti-p105 did not label amnioti c laminin-5 or 804G matrix, but did label p105 in both keratinocyte co nditioned medium and fibroblast cytosol. J-18 labeled the 105-kD lamin in-5 gamma 2 chain in reduced keratinocyte proteins and a 400-kD lamin in-5 complex under non-reducing conditions, In contrast, anti-p105 lab eled p105 under both reducing and non-reducing conditions but did not label a 400-kD protein complex, Similarly, comparative immunoblotting on keratinocyte proteins using anti-p105 and anti-laminin-1 revealed n o commonly labeled protein bands. Electrophoretic fractionations by pr eparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis an d immunoblotting of these fractions revealed that the peak fractions o f keratinocyte proteins reactive with anti-p105 are different from tho se reactive with J-18, Furthermore, keratinocyte proteins fractionated by Mono Q anion-exchange chromatography revealed fractions immunoreac tive with anti-p105, whereas J-18 showed no reactivity with these frac tions, Two-dimensional gel electrophoresis and immunoblotting with ant i-p105 revealed p105 to be an acidic protein with isoelectric points b etween 5.7 and 6.3, distinct from the isoelectric points of laminin-5 gamma 2 chain. We conclude that p105 is an acidic protein located in t he lamina lucida and distinct from the truncated laminin-5 gamma 2 cha in and the laminin-1 family.