Abstract
Over the past decade, the number of membrane protein (MP) structures solved at the atomic resolution level by electron cryo-microscopy (cryo-EM) has increased dramatically [1]. Despite the impact of cryo-EM in MP structural biology, further technological developments are still required. A major limitation lies in the preparation of high-quality grids: general advices might be shared [2], but grid properties remain poorly reproducible and system-dependent.
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