11 research outputs found

    ํ”„๋กœํ…Œ์˜ด ๋ถ„์„๋ฒ•์„ ์ด์šฉํ•œ ๋ˆ„์—์ฒด์•ก ์ค‘์˜ ํ•ญ ์—์ดํŒŒํ† ์‹œ์Šค ๋‹จ๋ฐฑ์งˆ์˜ ๋ถ„๋ฆฌ ๋ฐ ๋™์ •

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    ํ•™์œ„๋…ผ๋ฌธ(์„์‚ฌ)--์„œ์šธ๋Œ€ํ•™๊ต ๋Œ€ํ•™์› :์‘์šฉํ™”ํ•™๋ถ€,2003.The addition of silkworm hemolymph to culture medium increases the longevity of insect and mammalian cells by inhibiting apoptosis. The apoptosis-inhibiting component of silkworm hemolymph was identified as a low molecular weight lipoprotein, which is so-called '30K proteins' of unknown function. In this study, 30K proteins isolated from silkworm hemolymph by gel-filtration chromatography were studied by proteome analysis. The 30K proteins were separated into five spots, and all five spots were identified as low molecular 30kDa lipoprotein(Clone PBMHPC-19) by using MALDI-TOF. As a part of our effort to characterize the anti-apoptotic proteins in silkworm hemolymph and understand the proteome of silkworm hemolymph, silkworm hemolymph polypeptides were analyzed by 2D-gel mapping. To enhance reproducibility and resolving power of two dimensional electrophoresis, innovative method that inhibited reoxidation of โ€“SH group was used. Compared with conventional method, in the sample treated by the new protocol a much larger number of spots is visible. The 2D-map of silkworm hemolymph was composed of over 30 Coomassie-stained protein spots. Among them, 16 spots were identified by MALDI-TOF. Silkworm hemolymph was composed of several charge isomers of differently modified isoforms of several proteins.Maste
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