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Foreword

A Tribute to Stephen Allan Baldwin

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Steve Baldwin

I am very sad to be writing this as it is not, as it should be if life was fair, to recognize the passing of Steve Baldwin at a great old age after many years of happy retirement. It is instead to record his untimely passing when he was still full of energy and life with many important contributions still ahead of him. Nevertheless, I want to pay tribute to him and celebrate his many achievements, detailed below in an affectionate obituary by his long-standing colleagues and friends Peter Henderson, Vincent Postis, Stephen Muench and Alison Baker. I have known Steve for a long time, but not terribly well. We met occasionally, as scientists do, at conferences, committee meetings and suchlike. On those occasions I always enjoyed his company, both for his scientific insights and generosity and also for his delightful and warm personality. When I saw Steve was going to be at the same meeting as me it always made it something to look forward to rather than a chore. In the last couple of years when I moved close to Leeds I met him a few times and was looking forward to many more such meetings.

From the perspective of Molecular Membrane Biology, Steve was a great supporter and a long time Editorial Board member during the years when Jack Lucy was Editor-in-Chief, a role in which Steve excelled due to his scientific expertise, good judgement and work ethic. I appreciate what he did in those years and also the more informal advice he gave me on a number of occasions. Steve will be missed by me and many, many others. If there is a “place” after this life then I am sure he will be appreciated just as much there! Over to you Peter, Vincent, Stephen and Alison ….

Stephen Allan Baldwin, known to his many friends and colleagues as Steve, passed away on 13 November 2014, aged 62. He grew up in Southport in Lancashire, one of three children. His father was an airline pilot and his mother, a potter. He developed interests in outdoor activities, natural history, and in chemistry, which he explored in their garden shed (remember those chemistry sets we used to play with?). In 1970 he won a Scholarship to Trinity College, Cambridge, to study the Natural Sciences Tripos, specializing in Biochemistry in his final year. Here he met Jocelyn from Norwich and New Hall, also studying Part II Biochemistry, and they married in 1973 after graduation. They remained in Cambridge while Steve undertook research for a PhD degree supervised by Richard Perham in the Biochemistry Department. In 1978 their first papers on purification and characterization of Fructose 1,6 bisPhosphate Aldolases were published in the Biochemical Journal (Baldwin & Perham, Citation1978), a journal where Steve continued to publish throughout his career (Huysmans et al., Citation2012).

Like many of us at that time, Steve and Jocelyn became part of the “brain-drain” and set off for the USA to work with Gus Lienhard on the purification and characterization of the glucose transport protein from human red blood cells. Thus was born Steve’s long-term interest in biological membranes, and his many contributions to the understanding of glucose transport in mammalian cells, and its role in insulin reception and diabetes. In 1981 they returned to London where they met Jack Lucy, another scientist working with biological membranes. Steve raised antibodies to the glucose transport protein he and Jocelyn had purified, and this enabled the ground-breaking sequence and putative structure of the human glucose transporter published with American collaborators in Science in 1985 (Mueckler et al., Citation1985).

Their two boys, Chris and Alex, were born in 1984 and 1986, and Steve took up a Senior Lectureship at the Royal Free Hospital in London in 1988 where he became a Reader in 1992. During this period a second focus of his lifelong research then evolved on the activities of nucleoside transport proteins, based on his early characterization of the process in mammalian erythrocytes. Again, he exploited antibodies to identify the protein involved; this generated sequence information from which the gene could be identified.

While refereeing a grant proposal of Peter Henderson’s on bacterial sugar transporters, Steve realized there was a profoundly important similarity between human and bacterial transport proteins, and so the first members of the Major Facilitator Superfamily were recognized. Peter and Steve published this together in Nature in 1987 (Maiden et al., Citation1987), and they collaborated on-and-off ever since – their most recent paper was in 2013 (Henderson & Baldwin, Citation2013). In 1992 Peter and his family moved to Leeds, and Steve and Jocelyn and the boys came in 1993. Steve and Peter have occupied neighbouring laboratories ever since, first in the then Biochemistry Department, and subsequently in the Astbury Building, as founding members of the subsequently very successful Astbury Centre for Structural Molecular Biology.

The great majority of Steve’s science was done independently and with a much wider group of collaborators from all over the world – Canada, USA, Chile, India, Pakistan, Malaysia, Spain, many European countries and most recently, China. Not to mention many UK Universities – including Imperial College London, Oxford, Cambridge, Bristol, Manchester, Glasgow, Edinburgh, Sheffield and York. With a group from Glasgow University, Steve led the Membrane Protein Structure Initiative out of which emerged important structures of proteins involved in peptide transport (Newstead et al., Citation2011). He was also a group leader in the European Drug Initiative for Channels and Transporters (EDICT), and was very successful in advancing studies on structures and activities of transporters of biomedical interest.

Steve’s research had an impact on many areas of membrane biology, especially in the clinical domain. If we had to single out his major contributions they would be in the early development of understanding diabetes, and in understanding the role of nucleoside transporters in cancer chemotherapy.

Steve served on the Editorial Boards of a number of journals. In 1993 he became an Associate Editor of Molecular Membrane Biology. Many of his externally refereed science papers and reviews were published there, including one issue devoted to the outcomes of the MPSI project (The Membrane Protein Structure Initiative of the BBSRC, Molecular Membrane Biology 2008;25(8):585–701); he was also a contributor to a subsequent issue describing outcomes of the EDICT project (The European Drug Initiative for Channels and Transporters of the EC, Molecular Membrane Biology 2013;30:150).

Steve loved his research. “Biochemistry is my hobby” he would say. Over 100 students and postdoctoral researchers trained under Steve’s supervision, and he rejoiced in the high quality of their research and the publications (more than 200) they produced together. Through working with Steve, their horizons broadened and their ambitions grew. The theses they presented for their PhD degrees and their successes in science and many other walks of life constitute a major legacy of his.

So why did everybody love working with Steve? Well, first the mercenary reason – he was brilliant at writing grant applications! He grasped the essence of what was wanted by the sponsors, he thought deeply about the relevant issues, and he composed a series of carefully-conceived and meticulous arguments. Very many of us are literally in his debt for these contributions to our professional well-being. This meticulous and thoughtful approach extended to all Steve’s activities. He was the exemplar of the “good citizen” of our Institution – supportive, inclusive, and collegiate. His enthusiasm and willingness to embrace and share new ideas and his breadth and depth of knowledge were exceptional. He had one infuriating fault! He turned self-deprecation and modesty into an art form. Before or after some brilliant contribution, insight, or assistance he would say in all sincerity what rubbish it was and likely to be. A favourite expression was “I am as useful as a chocolate teapot”. Nothing could be further from the truth.

But the real reason Steve left an impression on so many people can be found in the numerous personal tributes we have received; a very small number of which are paraphrased here:

Steve was as lovely a guy as he was a talented scientist

What a lovely man and fine scientist he was

He was an excellent scientist and a very pleasant colleague

Steve was a gentleman

Steve was a very fine man indeed and a wonderful scientist

Steve was such a warm and friendly individual with boundless enthusiasm for his science

An inspirational example of academic honesty and kindness for all those…. working under his supervision

He is the truly model scientist I wish myself to follow

This personal esteem comes from all backgrounds, from secretary to Nobel Laureate, from student to professor, from Chile to Japan, from Bristol to Aberdeen.

Unfortunately, Steve became ill only shortly after he took early “retirement” although he continued to work just as hard as previously continuing to develop his innovative science. Despite the various setbacks and difficult treatments that he had to suffer Steve persisted in keeping busy and it was humbling to see him coping with his illness.

Throughout Steve’s busy career Jocelyn was a partner in his research activities as well as providing the personal and family life he truly appreciated. To Jocelyn, Chris, Alex and all Steve’s family and friends, we offer our heartfelt sympathy at the loss of a great friend and mentor.

References

  • Baldwin SA, Perham RN. 1978. Novel kinetic and structural properties of the class-I D-fructose 1,6-bisphosphate aldolase from Escherichia coli (Crookes’ strain). Biochem J 169:643–652
  • Henderson PJF, Baldwin SA. 2013. This is about the in and the out. Nature Struct Mol Biol 20:654–655
  • Huysmans GH, Chan N, Baldwin JM, Postis VL, Tzokov SB, Deacon SE, et al. 2012. A urea channel from Bacillus cereus reveals a novel hexameric structure. Biochem J 445:157–166
  • Maiden MCJ, Davis EO, Baldwin SA, Moore DCM, Henderson PJF. 1987. Mammalian and bacterial sugar-transport proteins are homologous. Nature 325:641–643
  • Mueckler M, Caruso C, Baldwin SA, Panico M, Blench I, Morris HR, et al. 1985. Sequence and structure of a human glucose transporter. Science 229:941–945
  • Newstead S, Drew D, Cameron AD, Postis VL, Xia X, Fowler PW, et al. 2011. Crystal structure of a prokaryotic homologue of the mammalian oligopeptide-proton symporters, PepT1 and PepT2. EMBO J 30:417–426

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