tenosynovitis 发表于 2025-3-23 10:03:03
Reconstitution of Membrane Proteins into Nanodiscs for Single-Particle Electron Microscopy,ess to structural methodologies developed for soluble proteins. Here, we present the reconstitution of OprM membrane protein into nanodisc associated with a step of size-exclusion chromatography, an approach applicable to prepare IMPs for subsequent visualization by single-particle electron microscopy.Basilar-Artery 发表于 2025-3-23 16:06:54
http://reply.papertrans.cn/64/6304/630382/630382_12.pngmonochromatic 发表于 2025-3-23 20:49:41
http://reply.papertrans.cn/64/6304/630382/630382_13.png先兆 发表于 2025-3-23 23:14:15
http://reply.papertrans.cn/64/6304/630382/630382_14.pngTdd526 发表于 2025-3-24 06:10:17
http://reply.papertrans.cn/64/6304/630382/630382_15.png使虚弱 发表于 2025-3-24 06:48:43
http://reply.papertrans.cn/64/6304/630382/630382_16.png来就得意 发表于 2025-3-24 11:11:56
Direct Extraction and Purification of Recombinant Membrane Proteins from , Protoplasts,ne proteins (MPs), leading to the crystallization and structure determination for a variety of them. The actual overexpression of functional MPs achieved with this system is, however, often accompanied by the formation of a variable but significant proportion of misfolded and/or aggregated proteins去掉 发表于 2025-3-24 18:53:23
http://reply.papertrans.cn/64/6304/630382/630382_18.pngforebear 发表于 2025-3-24 20:15:33
http://reply.papertrans.cn/64/6304/630382/630382_19.pngdandruff 发表于 2025-3-24 23:35:40
Methyl-Specific Isotope Labeling Strategies for NMR Studies of Membrane Proteins,provide high sensitivity even in very large proteins, such as membrane proteins in a membrane-mimicking environment. In this chapter, we discuss the approach for labeling methyl groups in .-based protein expression, as exemplified with the mitochondrial carrier GGC.