Hugh Pelham

Laboratory of Molecular Biology (LMB) between 2006 and 2018.^[8]

translation in immature blood cells (Reticulocytes).^[9] His PhD was supervised by Richard J. Jackson and Tim Hunt,^[7] who went on to receive the Nobel Prize in Physiology or Medicine

Professor of Molecular Biology at the University of Cambridge since 2015.^[3]

Fellow of the Royal Society (FRS) in 1988.^[7] His certificate of election reads:

Distinguished for his contributions to protein biosynthesis, the control of gene activity and intracellular sorting. He developed a sensitive in vitro translation system, with which he discovered that naturally "leaky" termination codons exist in plant virus RNAs, and achieved the first correct synthesis and processing of viral polyproteins in vitro. He showed that the transcription factor TFIIIA, which is required in Xenopus oocytes for 5S rDNA transcription, binds to the gene product, %S RNA and is present in large amounts in oocytes. From studies on heat shock genes, he identified the first regulatory DNA sequence (the "Pelham" box) in a eukaryotic gene, proving this alone could confer heat inducibility on another gene. He has shown that this sequence is the binding site for a transcription factor which is modified by heat shock, thus establishing the basic mechanism of induction of these genes. He has clarified the function of heat shock proteins, finding that two of these reside in the lumen of the endoplasmic reticulum. This led to his discovery that a C-terminal amino acid sequence is a novel sorting signal, preventing proteins from being exported from the lumen of the endoplasmic reticulum.^[14]

King Faisal International Prize in 1996.^[1] He won the Louis-Jeantet Prize for Medicine in 1991 and the EMBO Gold Medal in 1989. He was awarded the Colworth Medal from the Biochemical Society in 1988 and elected a member of the European Molecular Biology Organization (EMBO) in 1985.^[15]